The Cambridge Structural Database: a quarter of a million crystal structures and rising
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High-resolution analysis of Zn(2+) coordination in the alkaline phosphatase superfamily by EXAFS and x-ray crystallographyCrystal structure of human alpha-tocopherol transfer protein bound to its ligand: implications for ataxia with vitamin E deficiencyX-ray crystallography: Assessment and validation of protein-small molecule complexes for drug discovery.A new generation of crystallographic validation tools for the protein data bankCrystal structure of human arginase I complexed with thiosemicarbazide reveals an unusual thiocarbonyl mu-sulfide ligand in the binuclear manganese clusterInhibition of human steroid 5beta-reductase (AKR1D1) by finasteride and structure of the enzyme-inhibitor complexCalpha-H...O = C hydrogen bonds contribute to the specificity of RGD cell-adhesion interactionsAmmonium O,O′-diethyl dithiophosphateCrystallographic model validation: from diagnosis to healingSwissParam: A fast force field generation tool for small organic moleculesAdding diverse noncanonical backbones to rosetta: enabling peptidomimetic designThe Diffraction Pattern Calculator (DPC) toolkit: a user-friendly approach to unit-cell lattice parameter identification of two-dimensional grazing-incidence wide-angle X-ray scattering dataStructural Insights into Binding of the Antifungal Drug Fluconazole to Saccharomyces cerevisiae Lanosterol 14α-Demethylase.Binding of Uridine 5‘-Diphosphate in the “Basic Patch” of the Zinc Deacetylase LpxC and Implications for Substrate Binding † , ‡The structural basis for the mutagenicity of O6-methyl-guanine lesionsHIV-1 Reverse Transcriptase Structure with RNase H Inhibitor Dihydroxy Benzoyl Naphthyl Hydrazone Bound at a Novel SiteStructural Analysis of Charge Discrimination in the Binding of Inhibitors to Human Carbonic Anhydrases I and IISolution structure and dynamics of DNA duplexes containing the universal base analogues 5-nitroindole and 5-nitroindole 3-carboxamideA comparison of vanadate to a 2'-5' linkage at the active site of a small ribozyme suggests a role for water in transition-state stabilizationUnusual Cu(I)/Ag(I) coordination ofEscherichia coliCusF as revealed by atomic resolution crystallography and X-ray absorption spectroscopyInfluence of the incorporation of a cyclohexenyl nucleic acid (CeNA) residue onto the sequence d(CGCGAATTCGCG)Crystal Structure of Human Liver 4-3-Ketosteroid 5 -Reductase (AKR1D1) and Implications for Substrate Binding and CatalysisStructural effects of nucleobase variations at key active site residue Ade38 in the hairpin ribozymeShort strong hydrogen bonds in proteins: a case study of rhamnogalacturonan acetylesterase.Structural and biochemical studies of TREX1 inhibition by metals. Identification of a new active histidine conserved in DEDDh exonucleasesThe role of molecular modeling in the design of analogues of the fungicidal natural products crocacins A and DStructural Characterization of the Molecular Events during a Slow Substrate–Product Transition in Orotidine 5′-Monophosphate DecarboxylaseThe Structural Basis for Recognition of the PreQ0 Metabolite by an Unusually Small Riboswitch Aptamer DomainThe X-ray Structure of RU486 Bound to the Progesterone Receptor in a Destabilized Agonistic ConformationCatalytic reaction mechanism of Pseudomonas stutzeri L-rhamnose isomerase deduced from X-ray structuresCrystal Structure of Fatty Acid Amide Hydrolase Bound to the Carbamate Inhibitor URB597: Discovery of a Deacylating Water Molecule and Insight into Enzyme InactivationUsing a conformation-dependent stereochemical library improves crystallographic refinement of proteinsStructure of a stacked anthraquinone–DNA complexComparison between the orthorhombic and tetragonal forms of the heptamer sequence d[GCG(xT)GCG]/d(CGCACGC)Differential Reactivity between Two Copper Sites in Peptidylglycine α-Hydroxylating MonooxygenaseThe crystal structure of the CeNA:RNA hybrid ce(GCGTAGCG):r(CGCUACGC)Structural Insights into the Anti-methicillin-resistant Staphylococcus aureus (MRSA) Activity of CeftobiproleOligomycin frames a common drug-binding site in the ATP synthase.Radiation damage reveals promising interaction positionCharacterization of a versatile organometallic pro-drug (CORM) for experimental CO based therapeutics
P2860
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P2860
The Cambridge Structural Database: a quarter of a million crystal structures and rising
description
2002 nî lūn-bûn
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2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
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2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
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name
The Cambridge Structural Database: a quarter of a million crystal structures and rising
@ast
The Cambridge Structural Database: a quarter of a million crystal structures and rising
@en
type
label
The Cambridge Structural Database: a quarter of a million crystal structures and rising
@ast
The Cambridge Structural Database: a quarter of a million crystal structures and rising
@en
prefLabel
The Cambridge Structural Database: a quarter of a million crystal structures and rising
@ast
The Cambridge Structural Database: a quarter of a million crystal structures and rising
@en
P921
P3181
P1476
The Cambridge Structural Database: a quarter of a million crystal structures and rising
@en
P2093
Frank H. Allen
P304
P3181
P356
10.1107/S0108768102003890
P407
P577
2002-05-29T00:00:00Z
2002-06-01T00:00:00Z