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  • International Union of Crystallography (IUCr)
  • American Association for the Advancement of Science (AAAS)
  • American Meteorological Society
  • 1995-1999  (4,207)
  • 1997  (4,207)
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  • 1995-1999  (4,207)
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  • 1
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 220-221 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A mannose-specific lectin from Calystegia sepium has been crystallized by the hanging-drop vapour-diffusion method using ammonium sulfate as precipitant. The needle-shaped crystals are orthorhombic, space group C2221 with cell dimensions a = 55.2(1), b = 55.9 (1), c = 196.1 (1) Å. Fresh crystals diffract to 1.9 Å resolution on a synchrotron radiation source. The asymmetric unit contains a dimer of two identical 16 kDa subunits with a packing density of 2.36 Å3 Da−1. Intensity data have been observed beyond 2.0 Å, but reasonable statistics restricted the usable range to 2.0 Å.
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  • 2
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 227-228 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Two crystal forms of component 1 (the MoFe protein) of nitrogenase from Klebsiella pneumoniae have been isolated and characterized. The triclinic form has cell dimensions a = 76.0, b = 109.6, c = 144.6 Å, α = 80.3, β = 74.9 and γ = 69.6°, diffracts to around 3.0 Å and has two molecules in the asymmetric unit. The monoclinic form belongs to space group P21 with a = 76.6, b = 127.8, c = 109.1 Å and β = 104.6° (frozen at 100 K), diffracts to 1.5 Å and has one molecule in the asymmetric unit. At this resolution the outstanding questions concerning the structure and the operation of the enzyme, in particular the linkage between the Fe4S4 units in the P clusters, the true geometry of the apparently trigonal Fe atoms in the FeMoco and the reduction site itself, should be answerable.
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  • 3
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 302-310 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Soybean leghemoglobin a is a small (16 kDa) protein facilitating the transport of O2 to respiring N2-fixing bacteria at low free-O2 tension. The crystal structure of soybean ferric leghemoglobin a nicotinate has been refined at 2.3 Å resolution. The final R factor is 15.8% for 6877 reflections between 6.0 and 2.3 Å. The structure of soybean leghemoglobin a (143 residues) is closely similar to that of lupin leghemoglobin II (153 residues), the proteins having 82 identical residues when the sequences are aligned. The new structure provides support for the conclusion that the unique properties of leghemoglobin arise principally from a heme pocket considerably larger and more flexible than that of myoglobin, a strongly ruffled heme group, and a proximal histidine orientation more favourable to ligand binding.
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  • 4
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: C-phycocyanin and allophycocyanin from the green alga Spirulina platensis were isolated and crystallized by gel-acupuncture techniques. A novel two-step chromatographic procedure was used for purification. Blue hexagonal crystals were obtained by diffusing magnesium chloride into the protein solution for a week, followed by diffusion of PEG 6000 in order to complete the reduction of the solubility of the protein in the capillary tube used as a growth cell. In the case of allophycocyanin, crystals with a size of 0.4 × 0.3 × 0.3 mm were characterized by X-ray diffraction. They belong to space group P6322 with unit-cell parameters a = b = 102.04, c = 131.22 Å. The crystals of C-phycocyanin belong to either space group P6 or P63 with unit-cell constants a = b = 182.38, c = 60.87 Å, α = β = 90, γ = 120°. The crystals diffract beyond 2.4 and 2.5 Å resolution, respectively, using a rotating anode as an X-ray source.
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  • 5
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A chromoprotein from Pleurotus salmoneostramineus L. Vass. has been purified and crystallized. The needle-shaped crystal has monoclinic space group C2 with the cell dimensions of a = 118.5, b= 59.7,0 c = 31.8 Å and β = 114°. The crystal diffracts to 1.8 Å resolution with a synchrotron radiation X-ray source.
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  • 6
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 345-347 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Ab inito quantum chemical calculations are performed to quantify the stabilizing role of long C—H···O=C contacts in nucleic acid base pairing, which was suggested by Leonard, McAuley-Hecht, Brown & Hunter [(1995). Acta Cryst. D51, 136–139]. For the Watson-Crick adenine-uracil pair, a contribution of about 6% to the total bond energy is obtained. This weakly bonding effect is primarily a result of electrostatic attraction between the total positive charge of adenine C(2)—H and the negative end of the dipole uracil O(2)=C.
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  • 7
    Electronic Resource
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 355-363 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A lysozyme isolated from the milk of a monotreme, the echidna, Tachyglossus aculeatus multiaculeatus, has been crystallized (space group P21, with unit-cell dimensions a = 37.1, b = 42.0, c = 38.1 Å, β = 91° and Z = 2) and the structure refined to an R value of 0.167 for all measured data in the resolution range 7.0–1.9 Å. It had previously been inferred from sequence homology with α-lactalbumins that echidna milk lysozyme (EML) would bind one calcium ion per molecule. This has been confirmed in the present study in which the largest peak in a difference Fourier synthesis is associated with a calcium ion. The calcium binding site of EML is very similar to that observed in baboon and human α-lactalbumins, and in a human lysozyme engineered to contain a calcium-binding site. The overall fold of the protein is similar to that of chick-type lysozymes. EML, like pigeon lysozyme, has only 125 residues terminating at a cysteine but in EML this forms a disulfide with a cysteine at residue 9 whereas the equivalent cysteine residue in all other lysozymes of known sequence occurs at position 6. These changes cause some minor structural rearrangements. The binding of calcium appears to have had little effect on the polypeptide backbone conformation and caused only small changes in the conformation of side chains coordinating the calcium ion. A homology modelling study [Acharya, Stuart, Phillips, McKenzie & Teahan (1994). J. Protein Chem. 13(6), 569–584] correctly predicted the overall structure of EML and the nature of its calcium binding site but generally failed to model some more subtle differences observed in the EML structure as evidenced by the fact that the homology model more closely resembles the starting structure from which the model was derived than it does the crystal structure.
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  • 8
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 406-418 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Copper-containing nitrite reductases (NiR's) have been conveniently subdivided into blue and green NiR's which are thought to be redox partners of azurins and pseudo-azurins, respectively. Crystal structures of two green NiR's have recently been determined. Alcaligenes xylosoxidans has been shown to have a blue-copper nitrite reductase (AxNiR) and two azurins with 67% homology both of which donate electrons to it effectively. The first crystal structure of a blue NiR (AxNiR) in its oxidized and nitrite-bound forms, with particular emphasis to the Cu sites, is presented. The Cu-Smet distance is the same as those in the green NiR's. Thus, the length of this interaction is unlikely to be responsible for differences in colour. Crystallographic data presented here taken together with structural data of other single Cu type-1 proteins and their mutants suggest that the displacement of Cu from the strong ligand plane is perhaps the cause for the differences in colour observed for otherwise `classical' blue Cu centre. Nitrite is observed binding to the catalytic Cu in a bidentate fashion displacing the water molecule, offering a neat rationalization for the XAFS observation that the type-2 Cu-ligand distances increase on nitrite binding as a result of increased coordination. These results are discussed in terms of enzyme mechanism.
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  • 9
    Electronic Resource
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 419-425 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The X-ray structure of crystal form IX of bovine pancre- atic ribonuclease A (space group P212121) is reported at 1.6 Å resolution. The structure was refined to an R factor of 15.0% and includes coordinates for two sulfate ions, four methanol molecules and 82 waters. The structure could be superimposed on the highest resolution crystal structure of bovine pancreatic fibonuclease available (in space group P21) with an r.m.s, difference in main-chain atomic positions of 0.51 Å. Most of the larger differences between the two structures could be related to crystal lattice contacts. Superposition of the new structure with eight other structures of ribonuclease in six crystal forms resulted in an r.m.s, deviation from the average structure of 0.43 Å for all main-chain atoms. This similarity among structures exists in spite of the fact that all nine molecules are in different crystal environments.
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  • 10
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 438-447 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Osmotic pressure, small-angle X-ray scattering and quasi-elastic light scattering were used to study the medium-range interaction potentials between macromolecules in solution. These potentials determine macromolecular crystallization. Calf eye lens γ-crystallins were used as a model system with the charge, and therefore the interactions, varied with pH. The second virial coefficient was determined under the same conditions with each of the three techniques. Osmotic pressure and quasi-elastic light scattering can be used conveniently in the laboratory to rapidly test the type of interactions (either attractive or repulsive) present in the solution. The measurement is direct with osmotic pressure, whereas with quasi-elastic light scattering, the directly measured coefficient is a combination of thermodynamic and hydrodynamic terms. X-rays, which require more sophisticated equipment such as synchrotron radiation facilities, can provide more detailed information on the interparticle potentials when models are used. At low ionic strength, two potentials were found necessary to account for the temperature and pH phase diagram as a function of protein concentration. The first potential is the van der Waals attractive potential that was previously shown to account for the fluid-fluid phase separation at low temperature. The second potential is an electrostatic coulombic repulsive potential which is a function of the protein charge and thus of the pH. The interaction trail could be followed at protein concentrations as low as 10 mg ml−1. The results as a whole are expected to be valid for all compact low molecular weight proteins at low ionic strength.
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  • 11
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 464-468 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of apo duck ovotransfemn (APODOT) has been determined at a resolution of 4.0 Å by the molecular replacement method using the structure of duck ovotransfemn (DOT) as the search model. The DOT structure contains two iron binding sites; one in the N-terminal lobe lying between domains N1 and N2 and one in the C-terminal lobe between domains C1 and C2. Both lobes have a closed structure. Models of various forms of both the N and C lobes were used in the search. The final model was refined to give an R factor of 0.22. The comparison of the structure of APODOT with that of DOT shows that both the N and the C lobes are in an open form, where the N2 and C2 domains undergo large rigid-body rotations of 51.6 and 49.9° relative to the N1 and C1 domains, respectively. The interface between the N and C lobes, which is formed by the N1—C1 contact in the core of the molecule does not change significantly. The DOT molecule may be described in terms of three rigid bodies; the N1 and C1 domains as one rigid body forming the static core of the molecule and the N2 and C2 domains as two other rigid bodies which, on the release of iron, move away from the static core of the molecule to form the open structure of APODOT.
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  • 12
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 472-473 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: PR1A3 antibody binds specifically to the tumour-associated cell-surface antigen, carcinoembryonic antigen. Crystals of the Fab fragment of the PR1A3 antibody were obtained by vapour diffusion against mother liquor containing Tris–HC1 buffer, pH 8.6, magnesium chloride and polyethylene glycol 4000 as precipitating agent. Crystals belong to the monoclinic space group P21 with cell dimensions a = 42.2, b = 216.7, c = 45.9 Å and β = 95.6°. Two Fab fragments are proesent in the asymmetric unit. Diffracted intensities up to 2.9 Å resolution have been measured from frozen crystals.
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  • 13
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A strategy is presented for refining anomalous scattering models and calculating protein phases directly from the Bijvoet and dispersive differences of a macromolecular multiwavelength anomalous diffraction (MAD) experiment. This procedure, incorporated in the program MADPHSREF, is especially amenable for exploiting the weak perturbations to normal scattering produced by inner-shell electronic transitions of asymmetric metal and protein ligand assemblies. The protocol accounts for more than one type of anomalous scatterer, incorporates stereochemical restraints, treats the data in local scaling groups, and partly compensates for correlated errors. Approximating maximum likelihood by averaging observation variances and covariances over all values of phase considerably improved error estimation. Probabilistic rejection of aberrant observations, re-evaluated before each refinement cycle, improved refinement convergence and accuracy compared with other less flexible rejection criteria. MADPHSREF allows the facile combination of MAD phase information with phase information from other sources. For the suifite reductase hemoprotein (SiRHP), relative weights for MAD and multiple isomorphous replacement (MIR) phases were determined by matching histograms of electron density. Accurate metal-cluster geometries and the associated errors in atomic positions can be determined from refinement against anomalous differences using normal scattering phases from a refined structure. When applied to MAD data collected on SiRHP, these methods confirmed the Fe4S4 cluster asymmetry initially observed in the refined 1.6 Å resolution structure and resulted in a MAD-phased, experimental, electron-density map that is of better quality than the combined MAD/MIR map originally used to determine the structure.
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  • 14
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 458-460 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The matrix protein, M1, of influenza virus strain A/PR/8/34 has been purified from virions and crystallized. The crystals consist of a stable fragment (18 kDa) of the M1 protein. X-ray diffraction studies indicated that the crystals are in space group P3121 or P3221, with a = 66.17, c = 135.30 Å. Vm calculations showed that there are two monomers in the asymmetric unit.
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  • 15
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 480-481 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Staphylokinase, a 17 kDa protein, produced by certain strains of Staphylococcus aureus functions as a fibrin-specific plasminogen activator. During its interaction with plasminogen, staphylokinase is converted into a low molecular weight form by loss of ten amino-terminal residues. This low molecular weight form of recombinant staphylokinase has been crystallized using the hanging-drop vapor-diffusion technique with polyethylene glycol 4000 as precipitant. Crystals belong to the orthorhombic space group C2221 with unit-cell dimensions a = 43.78, b = 59.86 and c = 103.25 Å and one molecule in the asymmetric unit. These crystals diffract to about 2.4 Å resolution.
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  • 16
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 482-484 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: RNA guanylyltransferase, or capping enzyme (E.C. 2.7.7.50) catalyzes the transfer of GMP from GTP to diphosphate-terminated RNA to form the cap structure GpppN. Chlorella virus capping enzyme expressed in E. coli has been purified, treated with GTP and crystallized. X-ray diffraction data have been collected from these crystals as well as for a mercury derivative obtained by soaking the crystals in thimerosal. Selenomethionine RNA guanylyltransferase was purified and crystallized in a similar fashion. The space group is C2221 and the cell parameters are a = 93.3, b = 214.9, c = 105.8 Å. Two Hg atoms and two subsets of Se atoms have been localized using difference Patterson and Fourier methods, suggesting that there are two molecules per asymmetric unit.
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  • 17
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 513-523 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The ferritins are a multigene family of proteins that concentrate and store iron in all prokaryotic and eukaryotic cells. 24 monomeric subunits which fold as four-helix bundles assemble to form a protein shell with 432 cubic symmetry and an external diameter of ∼130 Å. The iron is stored inside the protein shell as a mineralized core ∼80 Å in diameter. Recombinant amphibian red cell M ferritin crystallizes in ∼2 M (NH4)2SO4 at pH 4.6 in a space group that has not been reported previously. Electron microscopy, precession photography, Patterson and Fourier maps of the native protein and a UO{_2^{2+}} derivative, and simulations were used to determine that the unit-cell dimensions are a = b = 169.6, c = 481.2 Å, α = β = γ = 90° and the space group is P41212 or P43212. A preliminary model of the structure was obtained by molecular replacement, with amphibian red cell L ferritin as the model. In contrast to previously determined ferritin crystal structures which have intermolecular contacts at the twofold and threefold molecular axes, M ferritin crystals have a novel intermolecular interaction mediated by interdigitation of the DE loops of two molecules at the fourfold molecular axes.
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  • 18
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 713-719 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of orthorhombic crystals of monellin, a sweet protein extracted from African serendipity berries, has been solved by molecular replacement and refined to 2.3 Å resolution. The final R factor was 0.150 for a model with excellent geometry. A monellin molecule consists of two peptides that are non-covalently bound, with chain A composed of three β-strands interconnected by loop regions and chain B composed of two β-strands interconnected by an α-helix. The N terminus of chain A is in close proximity to the C terminus of chain B. The two molecules in the asymmetric unit are related by a non-crystallographic twofold axis and form a dimer, similar to those previously observed in other crystal forms of both natural and single-chain monellin. The r.m.s, deviation between the Cα atoms in the two independent molecules is 0.60 Å, while the deviations from the individual molecules in the previously reported monoclinic crystals are 0.50–0.57 Å. This result proves that the structure of monellin is not significantly influenced by crystal packing forces.
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  • 19
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 747-755 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Lysozyme has been crystallized using the ESA Advanced Protein Crystallization Facility onboard the NASA Space Shuttle Orbiter during the IML-2 mission. CCD video monitoring was used to follow the crystallization process and evaluate the growth rate. During the mission some tetragonal crystals were observed moving over distances of up to 200 μm. This was correlated with microgravity disturbances caused by firings of vernier jets on the Orbiter. Growth-rate measurement of a stationary crystal (which had nucleated on the growth reactor wall) showed spurts and lulls correlated with an onboard activity: astronaut exercise. The stepped growth rates may be responsible for the residual mosaic block structure seen in crystal mosaicity and topography measurements.
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  • 20
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The charge-density distribution in 1H+-adeniniumtrichlorozinc(II) has bcen determined from X-ray diffraction data collected to sin θ/λ = 1.32 Å−1 at 123 K. The electrostatic potential, isolated from the crystal lattice, and the deformation density in the nucleobase have been calculated following multipole refinements based on the rigid pseudoatom model of Stewart. These and the molecular dimensions have been compared with results from the charge-density study of adenine hydrochloride hemihydrate by Cunane & Taylor [Acta Cryst. (1993). B49, 524–530] to determine the effects of metal binding on the nucleobase. The main conclusions are that while the bond lengths and angles in the pyrimidine ring are similar, those in the imidazole ring are significantly perturbed on complexation; lone-pair electron density at N7 is observed in both structures and lies significantly off the plane of the nucleobases; the positive electrostatic potential of the complexed base extends much further from the molecule than in the uncomplexed one and the regions of negative potential at N3 and N7 are depleted in the complexed base. The observed enhancement of positive electrostatic potential in the nucleobase on binding to zinc is presented in support of a model for the mechanism of reversible unwinding of DNA in the presence of zinc ions.
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  • 21
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 787-788 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A mannose-specific agglutinin from garlic (Allium sativum) which forms part of a well conserved super-family of bulb lectins has been purified and crystallized by the hanging-drop vapour-diffusion technique, by equilibrating with a 20% solution of PEG 8000 in the presence of α-D-mannose. Crystals of the dimeric form of this protein are monoclinic C2 with unit-cell dimensions a = 203.2, b = 43.8, c = 79.3 Å and β = 112.4° and have two dimers in the asymmetric unit. Data have been collected to 2.4 Å resolution and the structure solved by molecular replacement using the coordinates of the snowdrop lectin as the search model.
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  • 22
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 795-797 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Chicken egg-white lysozyme was crystallized from ammonium sulfate over the pH range 4.0–7.8, with protein concentrations from 100 to 150 mg ml−1. Crystals were obtained by vapor-diffusion or batch-crystallization methods. The protein crystallized in two morphologies with an apparent morphology dependence on temperature and protein concentration. In general, tetragonal crystals could be grown by lowering the protein concentration or temperature. Increasing the temperature or protein concentration resulted in the growth of orthorhombic crystals. Representative crystals of each morphology were selected for X-ray analysis. The tetragonal crystals belonged to the P43212 space group with crystals grown at pH 4.4 having unit-cell dimensions of a = b = 78.71, c = 38.6 Å and diffracting to beyond 2.0 Å. The orthorhombic crystals, grown at pH 4.8, were of space group P21212 and had unit-cell dimensions of a = 30.51, b = 56.51 and c = 73.62 Å.
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  • 23
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Methionine aminopeptidase (MAP) from Pyrococcus furiosus (Pfu) has been crystallized in four different forms (A, B, C and D). Form A crystals belong to space group P21 with unit-cell dimensions a = 54.18, b = 85.72, c = 72.84 Å, β = 108.34°. Forms B, C and D belong to space group P62(4) with unit-cell dimensions a = 139.1, c = 63.7 Å for form B, a = 198.6, c = 243.8 Å for form C, and a = 111.0, c = 125.0 Å for form D. Forms A and D diffract to 2.9 Å, form B diffracts to 3.5 Å, and form C crystals diffract to 4.5 Å. Form A contains two molecules of MAP-Pfu per asymmetric unit. The binuclear metal center positions and a non-crystallographic twofold symmetry matrix has been determined for the form A crystals.
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  • 24
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 25
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    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 342-344 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Crystals of aryl acylamidase (E.C. 3.5.1.13) from tulip bulbs have been obtained by the hanging-drop vapor-diffusion method using polyethylene glycol (PEG) 8000 as a precipitant. The crystals belong to space group P212121 with unit-cell dimensions a = 68.7, b = 80.1 and c = 112.9 Å. Assuming two molecules of molecular weight of 34 kDa in the asymmetric unit, Vm is 2.28 Å3 Da−1, indicating a solvent content of approximately 46%. The intensity data have been collected to 2.5 Å resolution with an Rmerge of 0.067.
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  • 26
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    Acta crystallographica 53 (1997), S. 354-354 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 27
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    Acta crystallographica 53 (1997), S. 354-354 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 28
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    Acta crystallographica 53 (1997), S. 377-384 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Neutron diffraction combined with the deuterium-labelled molecular groups of biological and model membrane components allows one to detect with high accuracy the structure of these objects. Experiments of this kind are only possible at unique high-flux neutron sources, and the planning of neutron-diffraction experiments must take into account some special requirements primarily related to the duration of the experiment and the accuracy of estimation of membrane structure parameters as a result of finite time of the measurements. This paper deals with the question of statistical accuracy of the position x0 and width v of the distribution of deuterium labels in membranes along the normal of their plane, which are determined in a neutron diffraction experiment. It is shown that the accuracy of x0 and v estimation does not depend on membrane constitution. It is dependent only on the scattering amplitude of the deuterium label, the label position x0 and the distribution width v. Analytic calculations show that the statistical errors Δx0 and Δv are inversely proportional to the scattering amplitude of the label and, as usual, to the square root of measurement time. The question of Δx0 and Δv dependence on the number of structure factors used in the calculations of x0 and v is also studied. It is shown that, the accuracy of x0 estimation is approximately constant with down to four structure factors used, and, with the number of the factors below four, it deteriorates drastically. Analogous is the behaviour of Δv(hmax) relation with one exception: abrupt deterioration of the accuracy occurs beginning with five structure factors used. One does not have to measure the highest diffraction reflections which takes a much longer time compared with the first ones. It is an important result. All the problems mentioned above have also been considered for the case of two different deuterium labels in membranes.
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  • 29
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    Acta crystallographica 53 (1997), S. 448-455 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: wARP is a procedure that substantially improves crystallographic phases (and subsequently electron-density maps) as an additional step after density-modification methods such as solvent flattening and averaging. The initial phase set is used to create a number of dummy atom models which are subjected to least-squares or maximum-likelihood refinement and iterative model updating in an automated refinement procedure (ARP). Averaging of the phase sets calculated from the refined output models and weighting of structure factors by their similarity to an average vector results in a phase set that improves and extends the initial phases substantially. An important requirement is that the native data have a maximum resolution beyond \sim2.4 Å. The wARP procedure shortens the time-consuming step of model building in crystallographic structure determination and helps to prevent the introduction of errors.
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  • 30
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    Acta crystallographica 53 (1997), S. 461-463 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Electron-transferring flavoprotein from the rumen bacterium Megasphaera elsdenii is a heterodimer (Mr = 75 kDa) containing FAD as cofactor and functioning solely to mediate electron transfer between the prosthetic groups of other proteins. The enzyme was crystallized by the hanging-drop vapour-diffusion method using polyethylene glycol 4000 as precipitant. The crystals obtained belong to the space group P212121 with unit-cell dimensions of a = 58.75, b = 61.77 and c = 122.27 Å. Interestingly the crystals exhibit a low solvent content. Crystals diffracted to beyond 2.5 Å using synchrotron radiation.
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  • 31
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The calcium-binding domain of the small subunit of porcine calpain (domain VI) has been expressed in Escherichia coli, purified, and crystallized in the presence of Ca2+. Two crystal forms have been obtained by the vapor-diffusion method using PEG 6000 as the precipitant. Crystal form I, belonging to trigonal space group P3121 (or P3221) with cell dimensions a = b = 79.8, c = 57.08 Å, α = β = 90.0 and γ, = 120.0° diffracted to 2.8 Å. The second crystal form diffracts to 1.8 Å and belongs to monoclinic space group P21 with cell dimensions a = 50.1, b = 79.7, c = 57.1 Å and β = 91.2°.
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  • 32
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    Acta crystallographica 53 (1997), S. 485-487 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The Zn2+ β-lactamase from Bacteroides fragilis (E.C. 3.5.2.6) was overexpressed in Escherichia coli using an isopropylthiogalactoside-inducible T7 RNA polymerase expression system. Crystallization trials by the hanging-drop vapour-diffusion method have yielded two different crystal forms from two slightly different conditions. Crystals of form I belong to the monoclinic space group C2 with unit-cell dimensions a = 56.03, b = 43.98, c = 105.32 Å, β = 112° and diffracted only up to 4.0 Å. Crystals of form II are orthorhombic, space group P212121 with unit-cell dimensions a = 48.10, b = 98.05, c = 111.76 Å, diffract to at least 2.0 Å and are suitable for high-resolution structural analysis.
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  • 33
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    Acta crystallographica 53 (1997), S. 493-506 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: This paper reports the primary sequence and refined crystal structure of Pseudomonas fluorescens holoazurin. The crystal structure has been determined by molecular replacement on the basis of the molecular model of azurin from Alcaligenes denitrificans, and refined by the method of molecular dynamics simulation and energy-restrained least-squares methods. P. fluorescens was crystallized in the orthorhombic space group P21212〈inf/〉1 with unit-cell dimensions a = 31.95, b = 43.78, c = 78.81 Å. The asymmetric unit is composed of only one molecule. The final R value is 16.7% for 6691 reflections to a resolution of 2.05 Å. This azurin structure shows some interesting features at His35 and His83. Part of the main chain of strand 3 including His35 O are involved in the contact between two symmetrically related molecules. P. fluorescens is also compared with the other azurin structures in terms of primary sequence, crystal packing, solvent structure and Cu-site geometry. The difference in fluorescence decay behavior of two holoazurins from P. fluorescens and P. aeruginosa and the correlation between the fluorescence quenching and electron transfer are discussed.
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  • 34
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    Acta crystallographica 53 (1997), S. 540-543 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A method is proposed for improvement of local portions of electron-density maps. The main difference between this method and several other dummy-atoms techniques is that the dummy atoms are placed independently of the initial weak density and are not biased by it. An example of an application of the method is given.
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  • 35
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    Acta crystallographica 53 (1997), S. 535-539 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The physical basis of the conditional probability distributions of the quartet and of the triplet are investigated by means of the `Patterson' and `modulus' sum functions, respectively. From this study, a new conditional probability distribution of the triplet follows which has been tested on real data from three structures of different size. The empirically found distribution is compared with Cochran's closely related distribution.
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  • 36
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    Acta crystallographica 53 (1997), S. 599-604 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The major endoglucanase (35 kDa) from the thermophilic fungus Thermoascus aurantiacus has been purified from culture filtrates using an affinity method and the sequence for 35 N-terminal amino acids determined. This has allowed assignment of the enzyme to subtype A6 of family 5 endoglucanases. The enzyme has been crystallized as thick plates by the hanging-drop method using ammonium sulfate as precipitant. The crystals belong to space group P212121 with cell edges a = 76.4, b = 85.7 and c = 89.5 Å, with two molecules in the asymmetric unit, and diffract to 1.62 Å resolution using synchrotron radiation. The structure will be solved by isomorphous replacement.
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  • 37
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    Acta crystallographica 53 (1997), S. 780-781 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: SM3 antibody binds to a tumour-associated epitope on polymorphic epithelial mucin (PEM). Crystals of the Fab fragment of SM3 in complex with a peptide antigen were obtained by vapour diffusion against mother liquor containing acetate buffer, pH 6.5, cadmium chloride and polyethylene glycol (PEG) 4000 as precipitating agent. Crystals belong to the monoclinic space group P21 with cell dimensions a = 42.2, b = 83.9, c = 64.5 Å and β = 93.4°. One Fab-antigen complex is present in the asymmetric unit. Diffracted intensities up to 1.95 Å resolution have been measured from a frozen crystal using synchrotron radiation.
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  • 38
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    Acta crystallographica 53 (1997), S. 665-672 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The Cα positions for a protein can provide a scaffold for the reconstruction of more complete models. Reconstructions can be by manual rebuilding, from geometric solutions to the constraints on main-chain torsion angles or from databases of known protein structures. The last method is usually the most convenient and reliable. This paper describes a database reconstruction program, CALPHA, and assesses its accuracy and reliability by test reconstructions of well refined structures. Typically, backbone atoms are repositioned to within 0.3 Å of their original positions. This corresponds to regenerating main-chain torsion angles to within 15°. Uses of CALPHA for automating refinement procedures are discussed. In particular, the uses of Cα-only and rcconstructed polyalanine models of HIV-1 reverse transcriptase for cross-rotation and translation function searches are compared. The CALPHA polyalanine model is found to provide more selectivity for approximately correct orientations. The effect on the translation function is dependent on the resolution shell employed. It is expected that these observations will be applicable in other cases.
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  • 39
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    Acta crystallographica 53 (1997), S. 8-22 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of the 60 kDa E. coli sulfite reductase hemoprotein (SiRHP) was determined by using multiwavelength anomalous diffraction (MAD) to exploit the relatively small anomalous signals produced near the Fe K absorption edge from the protein's native Fe4S4 cluster and siroheme Fe atom. Because of systematic measurement error, generation of useful MAD data required rejection of outlying intensity observations that were only identified by careful manual scrutiny of the observed intensities and single parameter scaling among wedges of diffraction data. The key steps for obtaining effective phases were local anisotropic scaling between Bijvoet pairs and among wavelengths, extraction of phase information from unmerged observations, and refinement of the anomalous scattering model. Important factors for positioning the anomalous scattering model included removal of aberrant coefficients from Patterson syntheses, positional refinement of the Fe positions against MAD-derived normal-scattering amplitudes, and systematic searches of cluster orientation that attempted to optimize agreement between observed and calculated MAD intensities. To obtain MAD phases for reflections that were underdetermined for least-squares methods, parameters necessary for defining phase-probability distributions had to be estimated from the anomalous scattering model. The MAD phase distributions, when combined probabilistically with otherwise insufficient MIR phase information, led to the determination of the SiRHP structure. The techniques developed and lessons learned from the SiRHP MAD experiment should be applicable to the design of MAD experiments on other macromolecules.
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  • 40
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    Acta crystallographica 53 (1997), S. 49-55 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A procedure combining direct methods and solvent flattening to break the phase ambiguity intrinsic to the single isomorphous replacement (SIR) technique has been tested with the experimental SIR data of the known protein RNase Sa at 2.5 Å resolution. The use of direct methods provided better initial phases for the solvent-flattening procedure, while the solvent-flattening procedure greatly improved direct-method phases leading to a traceable Fourier map. A small subset of known phases at low resolution makes direct phasing of SIR data much easier. Accordingly a method for extending low-resolution phases to high-resolution ones is proposed making use of additional SIR information. This reduces the problem of finding a value in the range of 0–2π for each unknown phase to that of just making a choice between two possible values. Tests with the known protein RNase Sa showed that the method is able to extend phases from a resolution of 6 to 2.5 Å leading to an easily traceable Fourier map. The solvent-flattening technique and the combination of which with direct methods were used for the phase extension. Either procedure yielded reasonably good results, but on the whole, the result from the combination of direct methods with solvent flattening is better. Results of the latter procedure were further compared with that from direct phasing of the 2.5 Å SIR data and with that from phase extension by solvent flattening without SIR information. An improvement gained by the use of SIR information is evident.
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  • 41
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    Acta crystallographica 53 (1997), S. 105-107 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Recombinant rhamnogalacturonase A from Aspergillus aculeatus has been crystallized and X-ray diffraction data has been collected. Crystals were grown by the hanging-drop vapour-diffusion technique, under the conditions 10% PEG 8000, 0.05 M KH2PO4 and 0.1 M sodium acetate buffered at pH 3.5. The crystals diffract beyond 2.0 Å resolution and belong to one of the orthorhombic space groups I212121 or I222, with the unit-cell parameters a = 62.9, b = 125.4 and c = 137.0 Å. There is one molecule in the asymmetric unit and a solvent content of approximately 54%. The enzyme is highly glycosylated corresponding to 5.9 kDa.
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  • 42
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    Acta crystallographica 53 (1997), S. 114-115 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Recombinant cohesin-2, a unique type of protein-recognition domain from the cellulosome of Clostridium thermocellum, has been crystallized by the hanging-drop vapor-diffusion method. The crystals are monoclinic, space group C2 with unit-cell dimensions a = 79.91, b = 47.86, c = 51.13 Å, β = 126.77°. There is most likely to be one molecule per asymmetric unit, corresponding to a packing density of 2.16 Å3 Da−1. The crystals diffract to beyond 2.3 Å on a conventional laboratory rotating-anode source.
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  • 43
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    Acta crystallographica 53 (1997), S. 125-128 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Tobacco ringspot virus, a plant virus that is believed to fill an apparent niche in the evolution of picornavirus-like capsids, has been crystallized by vapor diffusion with potassium phosphate and polyethylene glycol buffered at pH 6.5 in a new crystal form. The monoclinic crystals belong to the space group C2 with unit-cell dimensions of a = 407.1, b = 399.7, c = 285.9 Å and β = 129.1° and diffract synchrotron radiation to 3.3 Å. One half of a virus particle constitutes the crystallographic asymmetric unit. The orientation of the virus particle in the unit cell was determined by the rotation function analysis of a partial data set that has been collected at CHESS using image plates. Development of a suitable phasing model for the high-resolution structure determination of TRSV with the real-space molecular replacement technique is now under way.
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  • 44
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    Acta crystallographica 53 (1997), S. 160-168 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The crystal structure of the 154-amino-acid form of human basic fibroblast growth factor (hbFGF154), probably representing the intact form of hbFGF as deduced from the open reading frame of hbFGF cDNA, was determined by X-ray crystallography and refined to a crystallographic residual of 19.0% for all data between 20.0 and 2.0 Å resolution. Crystals were obtained from recombinant hbFGF154 expressed in E. coli. hbFGF154 has the same overall structure as the N-terminus truncated 146-amino-acid form. The structure has a Kunitz-type fold and is built of 12 β-strands of which six antiparallel strands form a β-sheet barrel. In the structure it was possible to locate two additional residues at the N terminus and the last three C-terminal amino-acid residues, which seem to be disordered in all but one of the reported structures of the truncated form of hbFGF. The C-terminal amino-acid residues are part of the last β-strand through the formation of a hydrogen bond between the main-chain amide group of Ala152 and the carbonyl O atom of Pro28. An apparent phosphate ion is bound within the basic region on the surface of the molecule and has as ligands the side chains of Asn35, Arg128 and Lys133 and two water molecules. A slightly different hydrogen-bonding pattern to the phosphate ion is observed as compared with the sulfate ions in the truncated forms [Eriksson, Cousens & Matthews (1993). Protein Sci. 2, 1274–1284; Zhang, Cousens, Barr & Sprang (1991). Proc. Natl Acad. Sci. USA, 88, 3446–3450]. One molecule of β-mercaptoethanol forms a disulfide bridge to Cys77.
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  • 45
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    Acta crystallographica 53 (1997), S. 151-159 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of membrane-active antibiotic cyclodecapeptide gramicidin S in the crystals of its complex with urea, C60H92N12010.0.5[(NH2)2CO].7.94H20, has been investigated with three-dimensional X-ray data by the automatic sequential approximation method. The crystals are trigonal, space group P3121, a = 25.80(3), c= 21.49 (2) Å, Mr = 7968, calculated density = 1.088 mg m−3, Z = 1. Conventional R factor: R1 = 0.0943, wR2 = 0.2478 [I〉 2σ(I)]. The molecule possesses an antiparallel twisted β-structure, with turns involving the Phe-Pro peptides. The Orn side chains extend on one side of the sheet, while the non-polar Val and Leu side chains are located on the other face. One of the Orn residues (namely Orn2) is linked by an intermolecular hydrogen bond to the O atom of Phe4 residue, the other is free. The side chains of the Phe residues have trans orientation (χ1 ∼ 180°) and those of the Val, Orn, Leu residues, except those of Orn2, have the preferential gauche orientation with the χ1 angle close to 60. Two side chains show statistical disorder and conformation of the Pro residues is Cs—Cβ-exo. There is half a urea molecule and also 7.94 water molecules distributed on 13 positions for each antibiotic molecule. A partially occupied and poorly ordered alcohol molecule had been identified. The gramicidin S molecules are arranged around the 31 axis in the form of a left-handed double spiral forming suggestive channels. The outer hydrophobic surface of the spiral is made of uncharged side radicals while the inside surface consists of the main-chain atoms, mainly O and N, and of ornithine side chains with N atoms at the ends. By changing the Orn side-chain conformation, the inner diameter of the channels may change from 3.4 to 6.3 Å. Thus, ions and particles of rather large size may pass through the channel. The possibility of the creation of the gramicidin S channels in mitochondrial membranes has been noted by some biochemists. The channel complexes are close-packed in a hexagonal arrangement in the crystal. The CI− ions, present in abundance in the mother solution, are not found ordered in the crystals, which may indicate the absence of the charges in the terminal N atoms of the Orn residues.
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  • 46
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    Acta crystallographica 53 (1997), S. 200-202 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Calgranulin C (CAGC) from pig granulocytes has been crystallized and X-ray diffraction data have been collected to 2.6 Å resolution. The crystals belong to the trigonal system, space group P3121 or P3221, cell parameters a = b = 54.35 (2), c = 141.32 (5) Å and probably contain two molecules in the asymmetric unit. CAGC is amongst the first reported typical S100-1ike calcium-binding protein to be crystallized and studied by X-ray crystallography.
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  • 47
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    Acta crystallographica 53 (1997), S. 197-199 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Cytochrome b562 from Erwinia chrysanthemi has been crystallized using the hanging-drop vapour-diffusion method with ammonium sulfate as the precipitant. X-ray precession photographs show that the crystals formed belong to either of the enantiomorphic space groups P41212 or P43212 with the cell parameters a = b = 98.6 and c = 62.7 Å. Estimation of the crystal density and consideration of the possible values for Vm indicate that there is either a dimer or trimer in the asymmetric unit. Experiments using the synchrotron radiation source at the CCLRC Daresbury Laboratory have shown that the crystals diffract to at least 2.7 Å resolution. An analysis of the N-terminal sequence indicates that this cytochrome shows limited homology to the cytochrome b562 from E. coli. Determination of the structure will therefore allow analysis of the relationship between these two proteins.
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  • 48
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    Acta crystallographica 53 (1997), S. 103-104 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A new crystal form of PHO4 DNA-binding domain-DNA complex was obtained by the truncation of the N-terminal segment. This diffracts to a higher resolution than any forms reported previously. The present crystal belongs to orthorhombic space group P212121, with unit-cell dimensions a=53.51, b=68.30, c= 108.77 Å. The crystal contains one protein dimer-DNA complex in the asymmetric unit.
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  • 49
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The recombinant human plasminogen binding protein tetranectin (TN) and the C-type lectin CRD of this protein (TN3) have been crystallized. TN3 crystallizes in the tetragonal space group P42212 with cell dimensions a = b = 64.0, c = 75.7 Å and with one molecule per asymmetric unit. The crystals diffract X-rays to at least 2.0 Å resolution. A complete diffraction data set has been collected to 2.7 Å resolution. The crystals of TN, obtained by the vapour-diffusion reverse salting-in method at 280 K, are rhombohedral, space group R3, with the hexagonal axes a = b = 89.1, c = 75.8 Å, and diffract to at least 2.5 Å. A full data set has been collected to 3.0 Å. The asymmetric unit contains one monomer of TN. Molecular replacement solutions for TN3 and TN have been obtained using the structure of the C-type lectin CRD of rat mannose-binding protein as search model. The rhombohedral space group indicates that trimers of TN are formed in accordance with the observation of trimerization in solution.
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    Acta crystallographica 53 (1997), S. 112-113 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A killer toxin from a halotolerant yeast, Pichia farinosa strain KK1, was crystallized at high- and low-salt concentrations. Crystals from the high-salt solution belonged to the tetragonal space group P41212 or P43212, with unit-cell dimensions of a = b = 81.10, c = 118.46 Å. The low-salt solution provided crystals that belonged to the same space group, with nearly same cell dimensions. Preliminary diffraction studies showed that the intensity distributions are significantly different between the two crystals. Both types of crystals contained either two or three molecules per asymmetric unit. They diffracted X-rays beyond 2.0 Å resolution and were stable to X-ray irradiation.
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Jacalin and artocarpin, the two lectins from jackfruit (Artocarpus integrifolia) seeds, have different physicochemical properties and carbohydrate-binding specificities. However, comparison of the partial amino-acid sequence of artocarpin with the known sequence of jacalin indicates close to 50% sequence identity. Artocarpin crystallizes in two forms, both monoclinic P21, with one and two tetramic molecules, respectively, in the asymmetric units of form I (a = 69.9, b = 73.7, c = 60.6 Å and β = 95.1°) and form II (a = 87.6, b = 72.2, c = 92.6 Å and β = 101.1°). Both the crystal structures have been solved by the molecular replacement method using the known structure of jacalin as the search model and one of them partially refined, confirming that the two lectins are indeed homologous.
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  • 52
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    Notes: The DNA methyltransferase M.BseC1 from B. stearothermophilus methylates the N6 atom of the 3′ adenine in the sequence 5′-ATCGAT-3′. The 579-residue protein has been isolated and crystallized using seeding and microdialysis techniques. The crystals are monoclinic, space group P21 with cell dimensions a = 53.7, b = 85.7, c = 151.8 Å and β = 95.1°, two molecules in the asymmetric unit and diffract to at least 2.5 Å resolution.
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  • 53
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    Acta crystallographica 53 (1997), S. 491-491 
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  • 54
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    Acta crystallographica 53 (1997), S. 492-492 
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  • 55
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    Acta crystallographica 53 (1997), S. 507-512 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Insulin has a concentration of 10−8–10−11 M in the blood which ensures that it circulates and exerts its physiological functions in vivo as a monomer. The crystal structure of monomeric porcine desB1-B2 despentapeptide (B26–B30) insulin (DesB1-2 DPI) with Mr = 4934 Da has been determined at 1.65 Å resolution using the molecular replacement method. A structural comparison between DesB1-2 DPI and 2Zn insulin reveals that the conformation of DesB1-2 DPI is more similar to molecule I than molecule II of 2Zn insulin. The remarkable conformational difference between B25-Phe in DesB1-2 DPI and B25-Phe in despentapeptide (B26–B30) insulin (DPI) indicates that the residue B25-Phe possesses great flexibility and mobility.
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  • 56
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    Acta crystallographica 53 (1997), S. 615-618 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The N-terminal domain of hnRNP A1 protein, termed UP1, comprises two tandem RNA-recognition motifs, both of which are necessary for efficient RNA binding and for the alternative splicing activity of hnRNP A1. Recombinant human UPI expressed in E. coli has been crystallized in space group P21 with unit-cell dimensions a = 37.94, b = 43.98, c = 55.64 Å and β = 93.9°. The unit-cell volume is consistent with one UP1 molecule per asymmetric unit and a calculated 49% solvent content. The crystal diffraction limit is higher than 1.3 Å, and a data set to 2.0 Å has been collected. Diffraction data from one platinum and two mercury derivatives have also been collected.
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  • 57
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    Acta crystallographica 53 (1997), S. 626-626 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Owing to a printing error, the text of §§3.2 and 3.3 of this article [Mathiesen & Mo (1997). Acta Cryst. D53, 262–268] was printed incorrectly. Pages 261–268, incorporating the correct versions of §§3.2 and 3.3, are reprinted on the following pages.
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  • 58
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    Acta crystallographica 53 (1997), S. 673-681 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A computer package ANOMIR is described which can derive phases from anomalous scattering and/or isomorphous-replacement data in any combination. For anomalous scattering it incorporates five methods of applying one-wavelength data and three methods for multiple-wavelength data including SPIN, reported here for the first time. In addition there are three procedures for multiple-wavelength data – the first modifying data for different wavelengths to make them mutually consistent, the second estimating the contributions of the anomalous scatterers alone and the third which finds anomalous differences. For single isomorphous replacement or one-wavelength anomalous scattering the phase ambiguity can be resolved by the direct method [Fan, Han, Qian & Yao (1984). Acta Cryst. A40, 489– 495] but for multiple isomorphous replacement the main method is an adaptation of the probability-curve method [Blow & Crick (1959). Acta Cryst. 12, 794–802]. A new statistical method is described for estimating the standard error in measuring magnitudes which is independent of having subsets of centric reflections. A method is described whereby the weights associated with phase estimates are used to generate probability curves, through which it is possible to combine estimates from different methods and to produce a `best phase' and figure-of-merit for every reflection. ANOMIR procedures are also available for handling combinations of one-wavelength anomalous scattering with single- or multiple-isomorphous replacement. A final process, which is always beneficial, is a single parallel application of the tangent formula. The ANOMIR package has been designed for easy use and is controlled throughout by KEYWORDS. Results for several structures are given and compared with those found from the MLPHARE program in the CCP4 package.
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  • 59
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    Acta crystallographica 53 (1997), S. 544-550 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Diffraction data to 5 Å resolution were collected on a myoglobin crystal at 80, 130, 180 and 240 K. The linear coefficient of thermal expansion for myoglobin was determined to be 45 × 10−6 K−1, based on the measured expansion of the unit-cell parameters. The nature of the hydration layers surrounding the protein in the crystal is described in terms of a shell solvent model, which was used to calculate the coefficient of thermal expansion in reasonable agreement with the measured value. Wilson statistics were calculated and discussed in terms of an averaged disorder model. [F(T2) − F(80 K) exp(−iφ)] Fourier maps were calculated where T2 was taken as 130, 180 and 240 K, respectively. None of these difference maps showed any features above 2.0σ in the protein region. The 130 and 240 K difference maps showed many small and widely distributed negative difference features and showed very few positive difference features above 2.5σ in the solvent region. However, the 180 K difference map showed an extensive negative difference feature at the interface between symmetry-related molecules, occurring in the vicinity of residues 40-50 on one molecule and 76-80 on a symmetry-related molecule. These difference neutron Fourier maps indicate a concerted effect at 180 K, which is interpreted in terms of an onset of extended lattice disorder.
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  • 60
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    Acta crystallographica 53 (1997), S. 580-587 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Horse-spleen apoferritin is known to crystallize in three different space groups, cubic F432, tetragonal P4212 and orthorhombic P21212. A structure comparison of the cubic and tetragonal forms is presented here. Both crystal forms were obtained by the vapor-diffusion technique and data were collected at 2.26 Å (cubic crystal) and 2.60 Å (tetragonal crystal) resolution. Two main differences were observed between these crystal structures: (i) whereas intermolecular contacts only involve salt-bridge type interactions via cadmium ions in the cubic structure, two types of interactions are observed in the tetragonal crystal (cadmium-ion-mediated salt bridges and hydrogen-bonding interactions) and (ii) cadmium ions bound in the threefold axes of ferritin molecules exhibit lower site-occupation factors in the tetragonal structure than in the cubic one.
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  • 61
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    Notes: The laccase from the fungus Coprinus cinereus has been prepared and crystallized in a form suitable for X-ray diffraction analysis. Small plate-like crystals of an enzymatically deglycosylated form of the enzyme have been grown by the hanging-drop method using polyethylene glycol as precipitant. These crystals diffract to at least 2.2 Å. They belong to the space group P212121 with cell dimensions a = 45.4, b = 85.7, c = 143.1 Å with a single molecule of laccase in the asymmetric unit.
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  • 62
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    Notes: The extracellular thermostable xylanase (XT-6) produced by the thermophilic bacterium Bacillus stearothermophilus T-6 was shown to bleach pulp optimally at pH 9 and 338 K, and was successfully used in a large-scale biobleaching mill trial. The xylanase gene was cloned and sequenced. The mature enzyme consists of 379 amino acids with a calculated molecular weight of 43 808 and pI of 9.0. Crystallographic studies of XT-6 were initiated to study the mechanism of catalysis as well as to provide a structural basis for rational introduction of enhanced thermostability by site-specific mutagenesis. This report describes the crystallization and preliminary crystallographic characterization of the native XT-6 enzyme. The most suitable crystals were obtained by the vapor-diffusion method using ammonium sulfate and 2-methyl-2,4-pentanediol as an organic additive. The crystals belong to a primitive trigonal crystal system (space group P31 or P32) with room-temperature cell dimensions of a = b = 114.9 and c = 122.6 Å. At 103 K the volume of the unit cell decreased significantly with observed dimensions of a = b = 112.2 and c = 122.9 Å. These crystals are mechanically strong and diffract X-rays to better than 2.2 Å resolution. The crystals exhibit considerable radiation damage at room temperature even at relatively short exposures to X-rays. A full 2.3 Å resolution diffraction data set (99.8% completeness) has recently been collected on flash-frozen crystals at 103 K using synchrotron radiation. Two derivatives of XT-6 were recently prepared. In the first derivative, a unique Cys residue replaced Glu265, the putative nucleophile in the active site. The second derivative was selenomethionyl xylanase which was produced biosynthetically. These derivatives have been crystallized and the resulting crystals were shown to be isomorphous to the native crystals and diffract X-rays to comparable resolutions.
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  • 63
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    Acta crystallographica 53 (1997), S. 650-657 
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    Notes: The turkey-egg lysozyme (TEL) complex with tri-N-acetylchitotriose [(GlcNac)3] was co-crystallized from 1.5% TEL and 2 mM (GlcNac)3 at pH 4.2. The crystal structure was determined by molecular replacement and refined to an R value of 0.182 using 10–1.77 Å data. The (GlcNac)3 molecule occupies the subsites A, B and C. At the subsites B and C, the sugar residues are bound in a similar manner to that found in the hen-egg lysozyme (HEL) complex. In contrast, the GlcNac residue at the subsite A is exposed to bulk solvent and has no contact with the protein molecule because the active residue Asp101 in HEL is replaced by Gly in TEL. A sulfate ion is bound in the vicinity of subsite B and forms hydrogen bonds with the sugar residue and the guanidino group of Arg61, assisting the binding of the sugar residue to subsite B. The active-site cleft of TEL is narrower than that of native TEL, thus attaining the best fit of the (GlcNac)3 molecule. The lack of binding ability of subsite A is discussed in relation to the catalytic properties of TEL. The result suggests that the cleavage pattern of oligosaccharide substrates in the catalytic reaction is regulated by the protein–sugar interaction at subsite A.
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  • 64
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    Notes: The novel furopyrimidine N-(4-{N-[(2,4-diaminofuro[2,3-d]pyrimidin-5-yl)methyl]methylamino}benzoyl)-L- glutamate (MTXO), a classical antifolate with antitumor activity comparable to that of methotrexate (MTX), has been studied as inhibitor–cofactor ternary crystal complexes with wild-type Pneumocystis carinii (pc) and recombinant human wild-type dihydrofolate reductase (hDHFR). These structural data provide the first direct comparison of the binding interactions of the same antifolate inhibitor in the active site for pc and human DHFR. The human ternary DHFR complex crystallizes in the rhombohedral space group R3 and is isomorphous to the ternary complex reported for a γ-tetrazole methotrexate analogue, MTXT. The pcDHFR complex crystallizes in the monoclinic space group P21 and is isomorphous to that reported for a trimethoprim (TMP) complex. Interpretation of difference Fourier electron-density maps for these ternary complexes revealed that MTXO binds with its 2,4-diaminofuropyrimidine ring interacting with Glu32 in pc and Glu30 in human DHFR, as observed for MTXT. The presence of the 6–5 furopyrimidine ring instead of the 6–6 pteridine ring results in a different bridge conformation compared with that of MTXT. The bridge torsion angles for MTXO, i.e. C(4a)—C(5)—C(8)—N(9) and C(5)—C(8)—N(9)—C(1′), are −156.5/51.9° and −162.6/51.8°, respectively for h and pc, compared with −146.8/57.4° for MTXT. In each case, the p-aminobenzoylglutamate conformation is similar to that observed for MTXT. In the pcDHFR complex, the active-site region is conserved and the additional 20 residues in the sequence compared with the human enzyme are located in external loop regions. There is a significant change in the nicotinamide ribose conformation of the cofactor which places the nicotinamide O atom close to the 4NH2 group of MTXO (2.7 Å), a shift not observed in hDHFR structures. As a consequence of this, there is a loss of a hydrogen bond between the nicotinamide carbonyl group and the backbone of Ala12 in pcDHFR. In the human ternary complexes, the cofactor NADPH is bound with a more extended conformation, and the nicotinamide O atom makes a 3.5 Å contact with the 4NH2 group of MTXO. Although the novel classical antifolate MTXO is not highly active against pcDHFR, there are correlations between its binding interactions consistent with its lower potency as an inhibitor of h and pcDHFR compared with MTX.
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  • 65
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    Acta crystallographica 53 (1997), S. 434-437 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A simple algorithm is described for the identification of spatially contiguous regions in crystallographic envelopes. In a single pass through the grid points of the envelope map, the occupied points are assigned to a series of locally contiguous sets based on consideration of the connections within single voxels. A spatially contiguous region is identified as the union of all of the locally contiguous sets that share an element in common. Therefore, chains of spatial connectivity are traced implicitly by performing simple set operations. This algorithm has been implemented in the program CNCTDENV as part of the DEMON/ANGEL suite of density-modification programs.
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  • 66
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    Acta crystallographica 53 (1997), S. 331-334 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A new cellular growth factor termed augmenter of liver regeneration (ALR) has been crystallized. ALR has been shown to have a proliferative effect on liver cells while at the same time producing an immunosuppressive effect on liver-resident natural killer cells and liver-resident mononuclear leukocytes. In addition, ALR appears to play an important role in the synthesis and stabilization of mitochondrial gene transcripts in actively regenerating cells. ALR crystals diffract to beyond 2 Å resolution and belong to space group P21212, with a = 125.1, b = 108.1 and c = 38.5 Å. Based on four molecules per asymmetric unit, the Matthews coefficient is calculated to be 2.16 Å3 Da−1 which corresponds to a solvent content of 43%.
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  • 67
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    Acta crystallographica 53 (1997), S. 524-534 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The measured macroscopic growth rates of the (110) face of tetragonal lysozyme show an unexpectedly complex dependence on the supersaturation. In earlier studies it has been shown that an aggregate growth unit could account for experimental growth-rate trends. In particular molecular packing and interactions in the growth of the crystal were favored by completion of the helices along the 43 axes. In this study the molecular orientations of the possible growth units and the molecular growth mechanism were identified. This indicated that growth was a two-step process: aggregate growth units corresponding to the 43 helix are first formed in the bulk solution by stronger intermolecular bonds and then attached to the crystal face by weaker bonds. A more comprehensive analysis of the measured (110) growth rates was also undertaken. They were compared with the predicted growth rates from several dislocation and two-dimensional nucleation growth models, employing tetramer and octamer growth units in polydisperse solutions and monomer units in monodisperse solutions. The calculations consistently showed that the measured growth rates followed the expected model relations with octamer growth units, in agreement with the predictions from the molecular level analyses.
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  • 68
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    Acta crystallographica 53 (1997), S. 551-557 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of toxin II from the scorpion Androctonus australis Hector has been determined ab initio by direct methods using SnB at 0.96 Å resolution. For the purpose of this structure redetermination, undertaken as a test of the minimal function and the SnB program, the identity and sequence of the protein was withheld from part of the research team. A single solution obtained from 1 619 random atom trials was clearly revealed by the bimodal distribution of the final value of the minimal function associated with each individual trial. Five peptide fragments were identified from a conservative analysis of the initial E-map, and following several refinement cycles with X-PLOR, a model was built of the complete structure. At the end of the X-PLOR refinement, the sequence was compared with the published sequence and 57 of the 64 residues had been correctly identified. Two errors in sequence resulted from side chains with similar size while the rest of the errors were a result of severe disorder or high thermal motion in the side chains. Given the amino-acid sequence, it is estimated that the initial E-map could have produced a model containing 99% of all main-chain and 81% of side-chain atoms. The structure refinement was completed with PROFFT, including the contributions of protein H atoms, and converged at a residual of 0.158 for 30 609 data with F ≥ 2σ(F) in the resolution range 8.0–0.964 Å. The final model consisted of 518 non-H protein atoms (36 disordered), 407 H atoms, and 129 water molecules (43 with occupancies less than unity). This total of 647 non-H atoms represents the largest light-atom structure solved to date.
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  • 69
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    Acta crystallographica 53 (1997), S. 571-579 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A Bayesian treatment for phase calculation in the multiwavelength anomalous diffraction (MAD) technique is presented. This approach explicitly treats effects of errors correlated among measurements at different wavelengths and between Bijvoet pairs. The resulting method, which is called Bayesian correlated MAD phasing, gives proper statistical consideration to all data and does not give special treatment to data from a particular wavelength. Results obtained using Bayesian correlated MAD phasing and two other strategies on both a model test case and on data obtained in two actual MAD experiments are compared. Although all procedures performed well when the completeness of the data was high, it is shown that Bayesian correlated MAD phasing is more robust with respect to incompleteness of data than the other methods are. At 60% completeness the improvement over other methods for the examples given was nearly 50% in the correlation coefficients, and made a substantial difference in the interpretability of an electron-density map.
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  • 70
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    Acta crystallographica 53 (1997), S. 720-723 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Crystals of a carotenoid protein from the cyanobacterium Arthrospira maxima have been grown in space group C2 with unit-cell dimensions a = 219.6, b = 40.3, c = 75.5 Å and β = 95.5°. The crystals diffract X-rays to 2.3 Å resolution and display unusual optical properties in polarized light that suggest that all of the carotenoid molecules in the crystals are oriented similarly. A slight increase in the concentration of a crystallization additive in the mother liquor induces macroscopic twinning, which is also visible when the crystals are illuminated with polarized light.
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  • 71
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    Acta crystallographica 53 (1997), S. 619-621 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Morphinone reductase from Pseudomonas putida M10, a flavoprotein involved in the degradation of morphine alkaloids, was purified from an overexpressing strain of Escherichia coli and crystallized using the hanging-drop vapour-diffusion method. Diffraction data were collected to 2.5 Å. The I-centred orthorhombic cell has a monomer in the asymmetric unit. Preliminary molecular replacement calculations have been performed using Old Yellow Enzyme as the search model.
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  • 72
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    Acta crystallographica 53 (1997), S. 627-637 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: This study attempts to examine the pattern and variability of backbone packing density in protein structures. A carefully selected non-redundant data set of known protein structures is analyzed in terms of amino-acid composition and the preference of individual amino acids to fall into regions of low, medium or high density depending on the number of observed non-sequence spatial neighbours. The relationship of the backbone packing density to a number of properties such as the hydrophobicity, non-bonded energies and secondary structural features of the amino acids are examined. The correlation between the average percentage composition and the percentage composition in regions corresponding to different levels of packing density of the proteins is evaluated. These studies are extended to the family of globins whose amino-acid sequences have diverged retaining the same three-dimensional structure during evolution. The significance of high-backbone-density regions in this family has become apparent as due to helix/helix packing. Further, the variation in the amino-acid composition in different contact regions of globin proteins follows the same pattern found for the general data set.
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  • 73
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    Acta crystallographica 53 (1997), S. 782-783 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The active non-glycosylated glucoamylase, overexpressed from the Saccharomycopsis fibuligera GLU1 gene in Escherichia coli BL21(DE3), has been purified from the solubilized inclusion bodies and then renatured in vitro. Crystals of the recombinant glucoamylase were obtained by vapour diffusion using PEG as precipitant. The crystals belong to the orthorhombic space group P212121, with unit-cell dimensions of a = 58.1, b = 87.8 and c = 99.9 Å, and diffract to 1.7 Å resolution. This is the first report of the crystallization of the full-length glucoamylase corresponding to the mature enzyme.
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    Acta crystallographica 53 (1997), S. 789-791 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A simple probability expression is derived to discriminate the intermolecular vectors in the cross rotation function. The radial weighting function introduced takes into account both particle anisometry and crystal packing and can be incorporated into existing molecular replacement packages.
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    Acta crystallographica 53 (1997), S. 807-808 
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    Acta crystallographica 53 (1997), S. 1-7 
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    Acta crystallographica 53 (1997), S. 41-48 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The results from refinements with six different weighting schemes in PROFFT, SHELXL93 and X-PLOR show that experimental weights, and especially unit weights, tend to overweight the low-angle data at the expense of the higher resolution data. This suggests that the use of unit weights are inappropriate except during initial cycles of refinements. Two alternative weighting schemes, one-line and two-line empirical weights, are shown to produce a relatively even distribution of the weighted r.m.s. error [r.m.s. Err = (\sum w \Delta F {^2}/n) {^1} {^/} {^2})] as a function of sin θ/λ and result in linear δ(R) normal probability plots. Free R values and free weighted r.m.s. errors from the refinement of a scorpion toxin structure show that the alternative weighting schemes are superior to unit weights, and the r.m.s. deviations of bond distances and angles from the target values and G factors, as calculated by PROCHECK, confirm the superiority of the empirical weighting scheme. It was also observed that changing the value of WA, the contribution of the X-ray gradient to the total function minimized, produced little variation in R free but was directly proportional to the r.m.s. deviation of the bond distances from the target values.
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  • 78
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    Acta crystallographica 53 (1997), S. 337-338 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Two distinct azurins named azurin-I and azurin-II were isolated from Alcaligenes xylosoxidans GIFU 1051 (AzG-I and AzG-II). They have been purified and crystallized. The crystals of AzG-I belong to the monoclinic crystal system, space group C2, unit-cell parameters a = 130.6, b = 54.4, c = 74.7 Å, β = 96.1°. The crystals of AzG-II belong to the tetragonal crystal system, space group P4122 or P4322, unit-cell parameters a = b = 52.6, c = 100.7 Å. Both crystals diffract up to 2.0 Å resolution and are suitable for X-ray crystallographic studies.
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  • 79
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    Acta crystallographica 53 (1997), S. 348-351 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: As part of the programme to understand the mechanism and specificity of lipase enzymes used in biotransformation reactions, the lipase from Candida cylindracea has been purified and crystallized. This lipase has been widely used by organic chemists for hydrolysis and esterification reactions. Crystals were obtained using polyethylene glycol 6000 as a precipitant and grew to 0.6 mm in the maximum dimension. The enzyme crystallized in the space group P21 with unit-cell dimensions a = 94.3, b = 117.0, and c = 114.2 Å with β = 109.2°. Calculations indicate that there are four molecules in the asymmetric unit. The crystals diffract to at least 2.5 Å resolution and the structure has been solved by molecular replacement using the lipase from Geotrichum candidum as a search model.
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  • 80
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    Acta crystallographica 53 (1997), S. 352-353 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Two crystal forms of 3-carboxy-cis,cis-muconate lactonizing enzyme from Pseudomonas putida have been characterized. Form A is in space group P6, with unit-cell dimensions a = b = 232, c = 79 Å, α = β = 90, γ = 120°. Form B is orthorhombic, with cell dimensions a = 163, b = 139, c = 90 Å α = β = γ = 90°.
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  • 81
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    Acta crystallographica 53 (1997), S. 371-376 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The chemical, physical and symmetry constraints of an electron-density map impose relationships between structure factors, and these relationships are exploited during refinement. However, constraints often allow an artificially high correlation between the model and the original structure factors, a flaw known as model or refinement bias. Elimination of the bias component of a constrained model, the component insensitive to constraints, enhances the power of phase-refinement techniques. The scale of the bias component, here denoted as γ, is shown to be equal in magnitude to the origin vector of the interference function G that defines the relationships between the structure factors. The γ correction leads to solvent flipping in the case of phase improvement by solvent flattening, and other types of constraint allow a similar treatment.
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  • 82
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    Acta crystallographica 53 (1997), S. 392-405 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 83
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    Acta crystallographica 53 (1997), S. 426-433 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Density-modification algorithms have gained, in recent years, a widespread use in the early stages of protein structure determination, especially in combination with the single isomorphous replacement, the multiple isomorphous replacement and the multiple-wavelength anomalous dispersion methods, where density modification usually leads to a significant improvement in the quality and interpretability of the initial electron-density map. The current computer programs which are used to perform this task combine several approaches, an important component of which is the solvent-flattening procedure. The latter procedure depends crucially on the correct determination of the molecular envelope. The solvent-flattening procedure has also been applied to the electron-density maps calculated from partial mod- els obtained from the molecular replacement method. In such case the envelope calculated in the standard way does not always encompass entirely the missing part. It has been found that the standard application of the density-modification method (as implemented by programs SQUASH and DM) to a map calculated from a molecular replacement model containing \sim60% of the molecule, led to little improvement in the map interpretability. Here, it is shown that a significant improvement of the map can be achieved when a better envelope is used in the procedure. Various methods of calculating the molecular envelope have been evaluated, the effect of the shape of the envelope on the modified electron-density map has been investigated and an improved procedure to calculate the envelope from a partial molecular replacement model is proposed.
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  • 84
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    Acta crystallographica 53 (1997), S. 456-457 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Using free-solution capillary electrophoresis, the electrophoretic mobility of µm-sized lysozyme crystals in their growth solution at 283 K, 1.5%(w/v) NaC1, and over a range of pH values between 3.59 and 5.70 has been measured. Under these conditions, the mobility is independent of crystal size, while the calculated zeta potential increases from +8 to +24 mV as the pH decreases. Since the pH dependence of the zeta potential mirrors the pH dependence of charge on the free molecule, as determined by acid titration, it is concluded that the charge on the crystal is a result of H+ adsorption from solution.
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  • 85
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    Acta crystallographica 53 (1997), S. 179-185 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A conceptually simple real-space convolution method has been developed which can be used to detect or enhance structural features in experimental macromolecular electron-density maps. The method has been implemented in a computer program (ESSENS). One application of the method is in selectively visualizing secondary-structure elements in multiple isomorphous replacement (MIR) maps of proteins, prior to map interpretation. This application is demonstrated for MIR maps of P2 myelin protein [Jones, Bergfors, Sedzik & Unge (1988). EMBO J. 7, 1597–1604; Cowan, Newcomer & Jones (1993). J. Mol. Biol. 230, 1225–1246] and glyoxalase I [Cameron, Olin, Ridderström, Mannervik & Jones (1997). In preparation]. Another application is in finding the optimal orientation and position of a known structural fragment (e.g. a protein domain or a ligand) in any type of electron-density map (real-space or phased molecular replacement). This application is demonstrated for the complex of acetylcholinesterase and the snake toxin fasciculin II [Harel, Kleywegt, Ravelli, Silman & Sussman (1995). Structure, 3, 1355–1366] where the toxin was located in a map phased using the molecular-replacement solution for the acetylcholinesterase alone.
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  • 86
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    Acta crystallographica 53 (1997), S. 186-194 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of a Fab fragment of a monoclonal antibody (1583) that neutralizes a broad range of HIV-1 isolates has been solved by X-ray crystallography. This antibody is directed against a poliovirus/HIV-I chimaera which presents a conserved epitope of the envelope protein gp41. Crystals of 1583 were obtained in the space group P212121 and the structure solved by molecular replacement. The model has been refined against all data in the range 10–2.9 Å to a final crystallographic R factor of 0.198. The antigen-binding site features a well defined groove, typical of antibodies that bind to small antigens, created in part by a relatively short CDR H3. The variable regions of 1583 were sequenced and, given the hydrophilic nature of the epitope, revealed a surprising lack of charged residues in the CDR's. However, the antigen-binding cleft is indeed very polar, due in part to the presence of two charged residues that emanate from outside the recognized CDR's.
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  • 87
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    Acta crystallographica 53 (1997), S. 195-196 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The recombinant asparginyl-tRNA synthetase from the thermophilic bacterium Thermus thermophilus expressed in Escherichia coli has been crystallized from PEG 6000 solutions. Depending on the PEG concentrations the crystals were in either tetragonal or hexagonal space groups. Although generally smaller, the latter (space group P6422) diffracted better, to a resolution of 2.8 Å. Using the coordinates of the yeast aspartyl-tRNA synthetase structure molecular replacement methods were applied to both tetragonal and hexagonal crystals; a solution was found which gave excellent crystal packing in both space groups.
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  • 88
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    Acta crystallographica 53 (1997), S. 203-206 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Through testing refinement protocols using free R-factor estimates of model quality, it is shown that real-space refinement can be a useful addition to conventional reciprocal-space refinement, even for protein structures with poor electron-density maps derived from multiple isomorphous replacement. By alternating real- and reciprocal-space refinements, starting with an experimental map, then calculating 2Fo - Fc maps, it is demonstrated with the structure of HMG-CoA reductase, that quick automatic refinement can yield a model with a free R factor 1.5% better than exhaustive reciprocal-space refinement, and within 1% of a model that was interactively rebuilt and refined repeatedly.
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  • 89
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    Acta crystallographica 53 (1997), S. 207-210 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A complex of the periplasmic chaperone FimC and the mannose-binding adhesin FimH from the Escherichia coli type 1 pilus system has been crystallized from ammonium sulfate solution using the hanging-drop vapour-diffusion method. The crystals diffract to a minimum Bragg spacing of 2.7 Å and belong to the space group P41212 or P43212 with cell dimensions a = b = 97.7, c = 215.9 Å at room temperature. Data to 3.0 Å have been collected from a single-crystal frozen to T = 100 K.
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  • 90
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    Acta crystallographica 53 (1997), S. 211-212 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: GM2 activator protein is a glycolipid transfer protein cofactor necessary for the hydrolytic degradation of GM2 ganglioside by β-hexosaminidase A. Its absence in human tissue results in symptoms of type AB Tay-Sachs disease. The protein prepared by recombinant techniques using an E. coli expression system, has been crystallized by the vapor-diffusion technique. The crystals are well ordered and belong to the orthorhombic space group P212121. The unit-cell dimensions are a = 42.40, b = 39.82, c = 113.61 Å. One molecule is contained in the asymmetric unit.
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  • 91
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    Acta crystallographica 53 (1997), S. 217-219 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: After many unsuccessful attempts to crystallize the bacteriophage lambda lysozyme, a mutant where all the tryptophan residues have been replaced by aza-tryptophans has been crystallized by the vapor-diffusion method. The crystals are orthorhombic and belong to space group P212121 with cell dimensions a = 73.01, b = 78.80, c = 82.31 Å. Diffraction data were collected using synchrotron radiation sources. Crystals diffract to a resolution of 2.3 Å. Data from two different platinum derivatives were also recorded to 2.8 and 2.5 Å, respectively.
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  • 92
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    Acta crystallographica 53 (1997), S. 229-230 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Crystals of xylose isomerase from the hyperthermophile Thermotoga neapolitana have been grown using the microbatch method under oil from solutions containing Jeffamine ED 4000 as precipitant. The space group of the crystals is C2221 with cell dimensions a = 161.8, b = 121.9, c = 98.9 Å and they contain two monomers in the asymmetric unit. The crystals diffract beyond 2.7 Å.
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  • 93
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    Acta crystallographica 53 (1997), S. 262-268 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of bovine pancreatic trypsin inhibitor could be re-determined both with data at 1.55 and 1.75 Å resolution using direct methods strengthened by the application of about 90 and 130 triplet phases, respectively, assumed known with a mean error of ±20°. From the known triplets a similar number of single phases were derived and used as starting values, thereby reducing or eliminating the need for permuting reflections in the starting set. The known triplets provide better estimates for the mean direction parameters in the corresponding Cochran distributions. This improvement is crucial for obtaining a structure solution. Single phases derived from these triplets could be combined to yield a larger set of triplets which forms the basis for a new figure of merit (FOM). The new FOM appears superior to the conventional ones for initial selection of the best phase model, and can also be used for assessing the correctness of structure expansion if the number of triplet phase relationships is sufficient.
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  • 94
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    Acta crystallographica 53 (1997), S. 256-261 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Xylanase from the bacterial plant pathogen Erwinia chrysanthemi (E.C. 3.2.1.8), expressed in E. coli, has been crystallized for X-ray diffraction analysis both in the presence and the absence of its polymeric substrate 4-O-methyl glucuronoxylan. In all cases it was found that the quality, time of appearance, and reproducibility of both the native and complex crystals were significantly enhanced by heating of the protein to 323 K prior to dispensing the crystallization trials. Crystals of the native protein are ideal for X-ray diffraction analysis, producing Bragg reflections beyond 1.5 Å resolution with virtually no degradation with time. The native crystals are in space group P21, with a = 39.33, b = 49.46, c = 90.85 Å and β = 101.58°. Other polymorphs have also been obtained and their cell parameters determined. Crystallization of the enzyme in the presence of polymeric substrate yields two distinctly different crystals at different concentrations of the xylan. These are thought to be complexes of the protein with stable products of the enzymatic reaction. A similar result had been obtained previously with pancreatic α-amylase and its substrate glycogen.
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  • 95
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    Acta crystallographica 53 (1997), S. 385-391 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A continuous procedure for replacing the 2 M (NH4)2SO4 within crystals of rabbit muscle phosphoglucomutase by 55% polyethylene glycol 600 (PEG 600) is described. The success rate (absence of fracturing) approaches 100% in spite of the fragility of the crystals. The procedure is based on the use of a biphasic PEG/salt mixture in conjunction with a flow cell that allows several crystals to be treated at once. The holdup volume of the cell is small and its design minimizes concentration gradients. Cooling treated crystals to 253 K elicits a substantial increase in diffractivity that allows data collection to be extended from about 2.75 to about 2.35 Å. However, neither the dimensions of the unit cell nor the structure of the asymmetric unit are significantly altered. Comparisons are made between data sets collected at 289 K using crystals in 2.2 M (NH4)2SO4 and at 253 K using crystals in 55% PEG 600. Models of the enzyme refined against one or the other data sets are also compared. These comparisons suggest that, at most, only a minor fraction of the increased diffractivity is caused by lowered atomic B values. The increased diffractivity also is not the result of a simple temperature effect since at high-salt concentration the same cooling protocol fails to significantly increase diffractivity. A decrease in mosaic spread is considered as a possible explanation for the increased diffractivity.
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  • 96
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    Acta crystallographica 53 (1997), S. 658-664 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Rhodobacter capsulatus strain St Louis cytochrome c′ (RCCP-SL) has been crystallized and the structure solved by molecular replacement. It was refined at 2.1 Å resolution to an R value of 18.4%, and compared with Rhodobacter capsulatus strain M110 cytochrome c′ (RCCP-M110). Although these two proteins are very similar in sequence and structure, the intermolecular interaction is largely different. In RCCP-M110, the molecules dimerize through interaction of helix B to form an antiparallel arrangement. When crystallized in the presence of Zn ions, molecules of RCCP-SL were found to be arranged as linear polymers connected by the bridging Zn ions. The changes in conformation of the side chains induced by binding of the Zn ions, by the substitution of Glu90 for Asp90, and by the different arrangement of the molecules, are discussed in detail.
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  • 97
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    Acta crystallographica 53 (1997), S. 682-690 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Several obstacles were encountered and overcome during the structure determination of human cytomega- lovirus protease. Dehydration of crystals, by exposing them to higher concentrations of the precipitant, reduced the mosaicity of the crystals and may have also resolved their microscopic twinning. The initial phase information was obtained with the selenomethionyl multiple-wavelength anomalous diffraction technique. However, site-specific mutagenesis was required to introduce extra Met residues into the protease. The phase information had to be improved by non-crystallographic symmetry averaging, initially among three `crystal forms'. A change in the composition of the artificial mother liquor led to a significant improvement, from 3.0 and 2.0 Å resolution, in the diffraction quality of the crystals. The experiences reported here may prove useful to structure determination of other proteins.
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  • 98
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    Acta crystallographica 53 (1997), S. 703-712 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Static and dynamic light scattering have been employed to investigate the behaviour of nucleating lysozyme solutions in the range between 0.34 and 3.08 mM. Preselected concentrations of NaC1 and (NH4)2SO4 have been used to screen the repulsive Coulombic interactions and trigger aggregation. Initially, mass-fractals undergoing diffusion limited-like aggregation coexist with monomers or small lysozyme oligomers. The growth kinetics of the fractals deliver observables that exhibit distinct tendencies when examined as a function of lysozyme concentration. The behaviour of the observables changes drastically around 2.0 mM lysozyme. Static light scattering experiments revealed progressive restructuring or growth of compact structures at later stages of the aggregation. Based on the correlations between the observables an attempt is made to predict whether the examined solutions will crystallize or not. A tentative scheme, involving the most prominent structures observed in nucleating lysozyme solutions, is discussed.
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    Acta crystallographica 53 (1997), S. 734-737 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: This paper describes an analysis of the optimum choice of the X-ray wavelength for macromolecular diffraction data collection. It is shown that there is no ultimate X-ray wavelength for protein crystallography and that the optimum wavelength depends to a large extent on the size of the protein crystal. It also depends on instrumental factors, such as efficiency of the detector for a particular wavelength and spectral density of the synchrotron radiation. Estimates of the optimum wavelength as a function of crystal size are given.
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    Acta crystallographica 53 (1997), S. 738-746 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Monoclinic crystals of nodamura virus (NOV) have two virus molecules per asymmetric unit. Packing analysis reveals a pseudo-rhombohedral (pseudo-C2 monoclinic) arrangement of particles in the actual P21 space group (a = 562.1, b = 354.1, c = 612.8 Å, β = 110.9°). The R32 symmetry is broken rotationally and translationally. The pseudo-symmetry of the unit cell results in three possible monoclinic origins and also restrains the four particles in the unit cell to similar orientations. NOV particles deviate by less than 3° from the ideal orientations, causing overlap of peaks in the rotation function and the generation of peaks that were not interpretable as particle symmetry elements. The space-group ambiguity was resolved by analysing the relationship between the particle orientations determined by high-resolution rotation functions and the attenuation of peak heights in native Patterson maps. Particles were centered less than 1 Å from the R32 special positions. Three different approaches were required to identify the correct particle center. Following the solutions of the rotation and translation problems, phases were computed using the coordinates of flock house virus (FHV), another member of this virus family. The phases were improved by real-space molecular averaging with a 120-fold non-crystallographic symmetry and by solvent flattening with a spherical mask. The final model for the NOV structure was built using the 3.3 Å averaged map. While the overall subunit structure was very similar to that of other nodaviruses, FHV and black beetle virus, NOV showed distinct structural features near particle threefold and quasi-threefold axes and at the protein–RNA interfaces that are consistent with phenotype differences among the related viruses.
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