about
High-affinity inhibitors of human NAD-dependent 15-hydroxyprostaglandin dehydrogenase: mechanisms of inhibition and structure-activity relationshipsSpecific recognition of a multiply phosphorylated motif in the DNA repair scaffold XRCC1 by the FHA domain of human PNKStructural basis of NEDD8 ubiquitin discrimination by the deNEDDylating enzyme NEDP1.Structure of the metal-independent restriction enzyme BfiI reveals fusion of a specific DNA-binding domain with a nonspecific nucleaseStructure of glutamate carboxypeptidase II, a drug target in neuronal damage and prostate cancerStructural basis of filopodia formation induced by the IRSp53/MIM homology domain of human IRSp53Binding of rasagiline-related inhibitors to human monoamine oxidases: a kinetic and crystallographic analysisCrystallographic Identification of a Noncompetitive Inhibitor Binding Site on the Hepatitis C Virus NS5B RNA Polymerase EnzymeIn Vitro Resistance Study of AG-021541, a Novel Nonnucleoside Inhibitor of the Hepatitis C Virus RNA-Dependent RNA PolymeraseA TyrCD1/TrpG8 hydrogen bond network and a TyrB10TyrCD1 covalent link shape the heme distal site of Mycobacterium tuberculosis hemoglobin O.Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structuresStaphostatins resemble lipocalins, not cystatins in foldFrom The Cover: Automated protein crystal structure determination using ELVESStructure and Kinetics of Monofunctional Proline Dehydrogenase from Thermus thermophilusCrystal Structure of Lysine Sulfonamide Inhibitor Reveals the Displacement of the Conserved Flap Water Molecule in Human Immunodeficiency Virus Type 1 ProteaseCrystal Structure and Computational Analyses Provide Insights into the Catalytic Mechanism of 2,4-Diacetylphloroglucinol Hydrolase PhlG from Pseudomonas fluorescensCa2+ release from the endoplasmic reticulum of NY-ESO-1-specific T cells is modulated by the affinity of TCR and by the use of the CD8 coreceptor.Design and Synthesis of HIV-1 Protease Inhibitors Incorporating Oxazolidinones as P2/P2‘ Ligands in Pseudosymmetric Dipeptide IsosteresComputational design and experimental study of tighter binding peptides to an inactivated mutant of HIV-1 proteaseCNK and HYP form a discrete dimer by their SAM domains to mediate RAF kinase signalingNonspecific base recognition mediated by water bridges and hydrophobic stacking in ribonuclease I fromEscherichia coliHIV-1 Protease Inhibitors from Inverse Design in the Substrate Envelope Exhibit Subnanomolar Binding to Drug-Resistant VariantsThe Structure of the Glial Cell Line-derived Neurotrophic Factor-Coreceptor Complex: INSIGHTS INTO RET SIGNALING AND HEPARIN BINDINGPortrait of an Enzyme, a Complete Structural Analysis of a Multimodular -N-Acetylglucosaminidase from Clostridium perfringensStructural and Functional Characterisation of a Conserved Archaeal RadA Paralog with Antirecombinase ActivityCrystal Structure of the Catalytic Domain of Drosophila β1,4-Galactosyltransferase-7Structures of hypoxanthine-guanine phosphoribosyltransferase (TTHA0220) fromThermus thermophilusHB8Structural and Kinetic Analysis of Bacillus subtilis N-Acetylglucosaminidase Reveals a Unique Asp-His Dyad MechanismStructure-Based Design, Synthesis, and Structure−Activity Relationship Studies of HIV-1 Protease Inhibitors Incorporating PhenyloxazolidinonesDrug resistance against HCV NS3/4A inhibitors is defined by the balance of substrate recognition versus inhibitor bindingThe C-Terminal Domain of the Arabinosyltransferase Mycobacterium tuberculosis EmbC Is a Lectin-Like Carbohydrate Binding ModuleApo- and cellopentaose-bound structures of the bacterial cellulose synthase subunit BcsZ.Molecular Mechanisms of Viral and Host Cell Substrate Recognition by Hepatitis C Virus NS3/4A ProteaseSelf-recognition mechanism of MamA, a magnetosome-associated TPR-containing protein, promotes complex assemblyStructure and Substrate Recognition of the Staphylococcus aureus Protein Tyrosine Phosphatase PtpATMC310911, a Novel Human Immunodeficiency Virus Type 1 Protease Inhibitor, Shows In Vitro an Improved Resistance Profile and Higher Genetic Barrier to Resistance Compared with Current Protease InhibitorsS1 Pocket of a Bacterially Derived Subtilisin-like Protease Underpins Effective Tissue DestructionStructural features underlying T-cell receptor sensitivity to concealed MHC class I micropolymorphismsSalt Bridges Regulate Both Dimer Formation and Monomeric Flexibility in HdeB and May Have a Role in Periplasmic Chaperone FunctionStructure ofN-formylglycinamide ribonucleotide amidotransferase II (PurL) fromThermus thermophilusHB8
P2860
Q21136072-E3CB0195-7B7B-42C5-9C20-C5604C15E5A9Q24318721-095B01B7-C120-444E-8AE2-F43342E82337Q24529121-AA913F72-DD1D-4400-94A6-F9CF328ACDA9Q24535057-E0E6ED35-2584-4D4C-B35C-EE2F103A97FCQ24542039-CCE4D8C7-C0BE-4943-8801-9C5BA228CE0EQ24557455-4E1D48DE-DCB1-4FBF-A1C7-E045C183A6BAQ24658203-68C7281D-7BDB-4E06-84CA-1ABAE924A1C9Q27477662-E1D0FEAC-1ADF-419C-8926-F1923AED6819Q27485335-312E405C-B37E-4D7A-B9D9-A1B4A0EB38D1Q27641095-4BE3CF1F-3626-493F-9DFD-6C7974AC6254Q27641832-EC980201-2A0F-44F6-BCB6-7D64E760A158Q27642197-3F03F803-1E18-4458-B946-AB0B66D6FC98Q27643057-26A4894E-7E99-4A15-BE70-E8ACF223BC05Q27644004-6E074B40-3C86-4F38-9CC9-99C5E26A3DEAQ27646453-9D42951F-1711-452B-9CF6-7E769C9ED5DEQ27646614-9CE75CD2-BAC7-480C-AE48-359F5D50F7A1Q27646628-A60E3E5D-3C50-447D-9B84-38DE19D6F00DQ27647177-D5EF8AA7-41B9-44D7-8134-64B74FEFFD53Q27647665-8DF26B68-7487-4516-B4CC-E4357A60E4B9Q27649887-FA90ED37-CFFC-4208-91CA-9E47E2E6754EQ27649953-471B35D5-3881-481D-A245-EE149CB5C527Q27650325-D428D527-096F-48AC-B898-6CF9937C9EDCQ27652467-4989C81A-F6B9-4470-9168-830EDDE1CC94Q27653649-0F70F781-D325-47A4-84F5-872452548463Q27655359-73F70766-00A1-4E35-A03C-77E2986E043EQ27660264-4A8A1B43-4C6A-4AE5-9425-6E504F0C35E2Q27663918-821EDD58-308A-47F4-BAAC-6ABE4EFFA39FQ27664387-5C554C79-277E-4C3A-903D-6EFE5A8649B9Q27665164-7401BABB-2AAF-4294-9055-0C2636724FE8Q27665956-89A13993-54B4-4349-BA5D-F6B64DE120BCQ27667217-C04CFAAA-53B6-47E0-BD41-71D0AF69BDA7Q27667380-7DDC9087-743B-443C-A697-BE2A0101CB41Q27667503-A84BA457-615D-4F86-B66D-F5C0756692CFQ27670972-49C94CC7-A9A5-4A7A-92A5-4FF0BFAF0BEEQ27672211-1BBE3C9E-18CB-4B68-A0F2-56174031EA0DQ27673331-4A559362-B6C4-41AF-BE2C-7FC50DDA0DB5Q27674974-89802FD2-9687-4E89-BB86-9E0B7EBFD81FQ27675160-B7E478FF-640E-4A72-B07D-2B381D173F38Q27675931-A58E00AB-FB29-4F75-90FF-BB347E4DEF5CQ27676671-14A92D5F-E392-4B3C-B61B-5CF5418D73B5
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
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
@wuu
name
ARP/wARP's model-building algorithms. I. The main chain
@ast
ARP/wARP's model-building algorithms. I. The main chain
@en
type
label
ARP/wARP's model-building algorithms. I. The main chain
@ast
ARP/wARP's model-building algorithms. I. The main chain
@en
prefLabel
ARP/wARP's model-building algorithms. I. The main chain
@ast
ARP/wARP's model-building algorithms. I. The main chain
@en
P2093
P1476
ARP/wARP's model-building algorithms. I. The main chain
@en
P2093
P304
P407
P433
P577
2002-06-01T00:00:00Z