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1AYU
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CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT SYMMETRIC BISCARBOHYDRAZIDE INHIBITOR
分子名称: 1,5-BIS(N-BENZYLOXYCARBONYL-L-LEUCINYL)CARBOHYDRAZIDE, CATHEPSIN K
著者Zhao, B, Smith, W.W, Janson, C.A, Abdel-Meguid, S.S.
登録日1997-11-10
公開日1998-11-25
最終更新日2023-08-02
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Design of potent and selective human cathepsin K inhibitors that span the active site.
Proc.Natl.Acad.Sci.USA, 94, 1997
1B1G
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SOLVATED REFINEMENT OF CA-LOADED CALBINDIN D9K
分子名称: CALCIUM ION, PROTEIN (CALBINDIN D9K)
著者Kordel, J, Pearlman, D.A, Chazin, W.J.
登録日1998-11-20
公開日1998-11-25
最終更新日2023-12-27
実験手法SOLUTION NMR
主引用文献Protein solution structure calculations in solution: solvated molecular dynamics refinement of calbindin D9k.
J.Biomol.NMR, 10, 1997
2CAU
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BU of 2cau by Molmil
CANAVALIN FROM JACK BEAN
分子名称: PROTEIN (CANAVALIN)
著者Ko, T.-P, Day, J, Macpherson, A.
登録日1998-11-20
公開日1998-11-25
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献The refined structure of canavalin from jack bean in two crystal forms at 2.1 and 2.0 A resolution.
Acta Crystallogr.,Sect.D, 56, 2000
1BBZ
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CRYSTAL STRUCTURE OF THE ABL-SH3 DOMAIN COMPLEXED WITH A DESIGNED HIGH-AFFINITY PEPTIDE LIGAND: IMPLICATIONS FOR SH3-LIGAND INTERACTIONS
分子名称: ABL TYROSINE KINASE, PEPTIDE P41, SULFATE ION
著者Pisabarro, M.T, Serrano, L, Wilmanns, M.
登録日1998-04-28
公開日1998-11-25
最終更新日2023-08-02
実験手法X-RAY DIFFRACTION (1.65 Å)
主引用文献Crystal structure of the abl-SH3 domain complexed with a designed high-affinity peptide ligand: implications for SH3-ligand interactions.
J.Mol.Biol., 281, 1998
16PK
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PHOSPHOGLYCERATE KINASE FROM TRYPANOSOMA BRUCEI BISUBSTRATE ANALOG
分子名称: 1,1,5,5-TETRAFLUOROPHOSPHOPENTYLPHOSPHONIC ACID ADENYLATE ESTER, 3-PHOSPHOGLYCERATE KINASE, 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID
著者Bernstein, B.E, Bressi, J, Blackburn, M, Gelb, M, Hol, W.G.J.
登録日1998-05-18
公開日1998-11-25
最終更新日2024-05-22
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献A bisubstrate analog induces unexpected conformational changes in phosphoglycerate kinase from Trypanosoma brucei.
J.Mol.Biol., 279, 1998
2BB8
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N-TERMINAL DNA BINDING DOMAIN FROM TN916 INTEGRASE, NMR, MINIMIZED AVERAGE STRUCTURE
分子名称: INTEGRASE
著者Clubb, R.T, Connolly, K.M, Wojciak, J.M.
登録日1998-05-12
公開日1998-11-25
最終更新日2024-05-22
実験手法SOLUTION NMR
主引用文献Site-specific DNA binding using a variation of the double stranded RNA binding motif.
Nat.Struct.Biol., 5, 1998
2BBY
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BU of 2bby by Molmil
DNA-BINDING DOMAIN FROM HUMAN RAP30, NMR, 30 STRUCTURES
分子名称: RAP30
著者Groft, C.M, Uljon, S.N, Wang, R, Werner, M.H.
登録日1998-04-27
公開日1998-11-25
最終更新日2024-05-22
実験手法SOLUTION NMR
主引用文献Structural homology between the Rap30 DNA-binding domain and linker histone H5: implications for preinitiation complex assembly.
Proc.Natl.Acad.Sci.USA, 95, 1998
1NSF
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BU of 1nsf by Molmil
D2 HEXAMERIZATION DOMAIN OF N-ETHYLMALEIMIDE SENSITIVE FACTOR (NSF)
分子名称: ADENOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, N-ETHYLMALEIMIDE SENSITIVE FACTOR
著者Yu, R.C, Hanson, P.I, Jahn, R, Brunger, A.T.
登録日1998-06-26
公開日1998-11-25
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Structure of the ATP-dependent oligomerization domain of N-ethylmaleimide sensitive factor complexed with ATP.
Nat.Struct.Biol., 5, 1998
4TMK
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BU of 4tmk by Molmil
COMPLEX OF E. COLI THYMIDYLATE KINASE WITH THE BISUBSTRATE INHIBITOR TP5A
分子名称: P1-(5'-ADENOSYL)P5-(5'-THYMIDYL)PENTAPHOSPHATE, PROTEIN (THYMIDYLATE KINASE)
著者Lavie, A, Ostermann, N, Schlichting, I.
登録日1998-08-31
公開日1998-11-25
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (1.98 Å)
主引用文献Structural basis for efficient phosphorylation of 3'-azidothymidine monophosphate by Escherichia coli thymidylate kinase.
Proc.Natl.Acad.Sci.USA, 95, 1998
1A70
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SPINACH FERREDOXIN
分子名称: FE2/S2 (INORGANIC) CLUSTER, FERREDOXIN
著者Binda, C, Coda, A, Mattevi, A, Aliverti, A, Zanetti, G.
登録日1998-03-19
公開日1998-11-25
最終更新日2024-05-22
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structure of the mutant E92K of [2Fe-2S] ferredoxin I from Spinacia oleracea at 1.7 A resolution.
Acta Crystallogr.,Sect.D, 54, 1998
1CQ4
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CI2 MUTANT WITH TETRAGLUTAMINE (MGQQQQGM) REPLACING MET59
分子名称: PROTEIN (SERINE PROTEINASE INHIBITOR 2), SULFATE ION
著者Chen, Y.W, Stott, K.R.
登録日1998-11-17
公開日1998-11-25
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Crystal structure of a dimeric chymotrypsin inhibitor 2 mutant containing an inserted glutamine repeat.
Proc.Natl.Acad.Sci.USA, 96, 1999
1AYW
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BU of 1ayw by Molmil
CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT BENZYLOXYBENZOYLCARBOHYDRAZIDE INHIBITOR
分子名称: 1-(N-BENZYLOXYCARBONYL-L-LEUCINYL)-5-(3-BENZYLOXY BENZOYL)CARBOHYDRAZIDE, CATHEPSIN K
著者Zhao, B, Smith, W.W, Janson, C.A, Abdel-Meguid, S.S.
登録日1997-11-10
公開日1998-11-25
最終更新日2023-08-02
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Design of potent and selective human cathepsin K inhibitors that span the active site.
Proc.Natl.Acad.Sci.USA, 94, 1997
1AOX
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I DOMAIN FROM INTEGRIN ALPHA2-BETA1
分子名称: INTEGRIN ALPHA 2 BETA, MAGNESIUM ION
著者Emsley, J, King, S.L, Bergelson, J.M, Liddington, R.C.
登録日1997-07-13
公開日1998-11-25
最終更新日2023-08-02
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Crystal structure of the I domain from integrin alpha2beta1.
J.Biol.Chem., 272, 1997
1AX8
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Human obesity protein, leptin
分子名称: OBESITY PROTEIN
著者Zhang, F, Beals, J.M, Briggs, S.L, Clawson, D.K, Wery, J.-P, Schevitz, R.W.
登録日1997-10-31
公開日1998-11-25
最終更新日2012-05-09
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Crystal structure of the obese protein leptin-E100.
Nature, 387, 1997
1B03
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SOLUTION STRUCTURE OF THE ANTIBODY-BOUND HIV-1IIIB V3 PEPTIDE
分子名称: PROTEIN (P1053 PEPTIDE)
著者Tugarinov, V, Zvi, A, Levy, R, Anglister, J.
登録日1998-11-17
公開日1998-11-25
最終更新日2023-12-27
実験手法SOLUTION NMR
主引用文献A cis proline turn linking two beta-hairpin strands in the solution structure of an antibody-bound HIV-1IIIB V3 peptide.
Nat.Struct.Biol., 6, 1999
1BCY
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RECOMBINANT RAT ANNEXIN V, T72K MUTANT
分子名称: ANNEXIN V, CALCIUM ION, SULFATE ION
著者Mo, Y.D, Swairjo, M.A, Li, C.W, Head, J.F, Seaton, B.A.
登録日1998-05-04
公開日1998-11-25
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (1.95 Å)
主引用文献Mutational and crystallographic analyses of interfacial residues in annexin V suggest direct interactions with phospholipid membrane components.
Biochemistry, 37, 1998
1B05
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Structure of oligo-peptide binding protein complexed with LYS-CYS-LYS
分子名称: PEPTIDE LYS-CYS-LYS, PERIPLASMIC OLIGOPEPTIDE-BINDING PROTEIN, URANIUM ATOM
著者Tame, J.R.H, Wilkinson, A.J.
登録日1998-11-20
公開日1998-11-25
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Crystallographic and calorimetric analysis of peptide binding to OppA protein.
J.Mol.Biol., 291, 1999
1QPN
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Quinolinate Phosphoribosyl Transferase from Mycobacterium Tuberculosis in Complex with NCNN
分子名称: NICOTINATE MONONUCLEOTIDE, PROTEIN (QUINOLINATE PHOSPHORIBOSYL TRANSFERASE)
著者Sharma, V, Grubmeyer, C, Sacchettini, J.C, TB Structural Genomics Consortium (TBSGC)
登録日1998-11-20
公開日1998-11-25
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Crystal structure of quinolinic acid phosphoribosyltransferase from Mycobacterium tuberculosis: a potential TB drug target.
Structure, 6, 1998
1LDZ
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SOLUTION STRUCTURE OF THE LEAD-DEPENDENT RIBOZYME, NMR, 25 STRUCTURES
分子名称: LEAD-DEPENDENT RIBOZYME
著者Hoogstraten, C.G, Legault, P, Pardi, A.
登録日1998-08-18
公開日1998-11-25
最終更新日2024-05-22
実験手法SOLUTION NMR
主引用文献NMR solution structure of the lead-dependent ribozyme: evidence for dynamics in RNA catalysis.
J.Mol.Biol., 284, 1998
1QPQ
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Structure of Quinolinic Acid Phosphoribosyltransferase from Mycobacterium Tuberculosis: A Potential TB Drug Target
分子名称: QUINOLINATE PHOSPHORIBOSYLTRANSFERASE, QUINOLINIC ACID, SULFATE ION
著者Sharma, V, Grubmeyer, C, Sacchettini, J.C, TB Structural Genomics Consortium (TBSGC)
登録日1998-11-20
公開日1998-11-25
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.45 Å)
主引用文献Crystal structure of quinolinic acid phosphoribosyltransferase from Mycobacterium tuberculosis: a potential TB drug target.
Structure, 6, 1998
1NLR
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ENDO-1,4-BETA-GLUCANASE CELB2, CELLULASE, NATIVE STRUCTURE
分子名称: ENDO-1,4-BETA-GLUCANASE
著者Sulzenbacher, G, Dupont, C, Davies, G.J.
登録日1997-10-27
公開日1998-11-25
最終更新日2022-12-21
実験手法X-RAY DIFFRACTION (1.75 Å)
主引用文献The Streptomyces lividans family 12 endoglucanase: construction of the catalytic cre, expression, and X-ray structure at 1.75 A resolution.
Biochemistry, 36, 1997
5TMP
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COMPLEX OF E. COLI THYMIDYLATE KINASE WITH THE BISUBSTRATE INHIBITOR AZTP5A
分子名称: P1-(5'-ADENOSYL)P5-(5'-(3'AZIDO-3'-DEOXYTHYMIDYL))PENTAPHOSPHATE, PROTEIN (THYMIDYLATE KINASE)
著者Lavie, A, Ostermann, N, Schlichting, I.
登録日1998-09-01
公開日1998-11-25
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (1.98 Å)
主引用文献Structural basis for efficient phosphorylation of 3'-azidothymidine monophosphate by Escherichia coli thymidylate kinase.
Proc.Natl.Acad.Sci.USA, 95, 1998
7MHT
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CYTOSINE-SPECIFIC METHYLTRANSFERASE HHAI/DNA COMPLEX
分子名称: 5'-D(P*CP*CP*AP*TP*GP*AP*GP*CP*TP*GP*AP*C)-3', 5'-D(P*GP*TP*CP*AP*GP*CP*GP*CP*AP*TP*GP*G)-3', CYTOSINE-SPECIFIC METHYLTRANSFERASE HHAI, ...
著者O'Gara, M, Horton, J.R, Roberts, R.J, Cheng, X.
登録日1998-08-05
公開日1998-11-30
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (2.87 Å)
主引用文献Structures of HhaI methyltransferase complexed with substrates containing mismatches at the target base.
Nat.Struct.Biol., 5, 1998
8MHT
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CYTOSINE-SPECIFIC METHYLTRANSFERASE HHAI/DNA COMPLEX
分子名称: 5'-D(P*CP*CP*AP*TP*GP*UP*GP*CP*TP*GP*AP*C)-3', 5'-D(P*GP*TP*CP*AP*GP*CP*GP*CP*AP*TP*GP*G)-3', CYTOSINE-SPECIFIC METHYLTRANSFERASE HHAI, ...
著者O'Gara, M, Horton, J.R, Roberts, R.J, Cheng, X.
登録日1998-08-06
公開日1998-11-30
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (2.76 Å)
主引用文献Structures of HhaI methyltransferase complexed with substrates containing mismatches at the target base.
Nat.Struct.Biol., 5, 1998
9MHT
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CYTOSINE-SPECIFIC METHYLTRANSFERASE HHAI/DNA COMPLEX
分子名称: 5'-D(P*CP*CP*AP*TP*GP*CP*GP*CP*TP*GP*AP*C)-3', 5'-D(P*GP*TP*CP*AP*GP*(3DR)P*GP*CP*AP*TP*GP*G)-3', CYTOSINE-SPECIFIC METHYLTRANSFERASE HHAI, ...
著者O'Gara, M, Horton, J.R, Roberts, R.J, Cheng, X.
登録日1998-08-07
公開日1998-12-01
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (2.39 Å)
主引用文献Structures of HhaI methyltransferase complexed with substrates containing mismatches at the target base.
Nat.Struct.Biol., 5, 1998

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