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1ANX
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THE CRYSTAL STRUCTURE OF A NEW HIGH-CALCIUM FORM OF ANNEXIN V
分子名称: ANNEXIN V, CALCIUM ION, SULFATE ION
著者Sopkova, J, Renouard, M, Lewit-Bentley, A.
登録日1993-10-26
公開日1994-12-20
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献The crystal structure of a new high-calcium form of annexin V.
J.Mol.Biol., 234, 1993
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
1BCK
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HUMAN CYCLOPHILIN A COMPLEXED WITH 2-THR CYCLOSPORIN
分子名称: CYCLOSPORIN C, PEPTIDYL-PROLYL CIS-TRANS ISOMERASE A
著者Mikol, V, Kallen, J, Taylor, P, Walkinshaw, M.D.
登録日1998-04-30
公開日1998-09-16
最終更新日2023-08-02
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献X-Ray Structures and Analysis of 11 Cyclosporin Derivatives Complexed with Cyclophilin A.
J.Mol.Biol., 283, 1998
1XPA
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BU of 1xpa by Molmil
SOLUTION STRUCTURE OF THE DNA-AND RPA-BINDING DOMAIN OF THE HUMAN REPAIR FACTOR XPA, NMR, 1 STRUCTURE
分子名称: XPA, ZINC ION
著者Ikegami, T, Kuraoka, I, Saijo, M, Kodo, N, Kyogoku, Y, Morikawa, K, Tanaka, K, Shirakawa, M.
登録日1998-07-06
公開日1999-07-22
最終更新日2024-05-22
実験手法SOLUTION NMR
主引用文献Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA.
Nat.Struct.Biol., 5, 1998
5UWW
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BU of 5uww by Molmil
Crystal Structure of DEAF1 Peptide in complex with CRM1 K579A mutant-Ran-RanBP1
分子名称: Deformed epidermal autoregulatory factor 1 homolog, Exportin-1, GLYCEROL, ...
著者Fung, H.Y.J, Chook, Y.M.
登録日2017-02-21
公開日2017-03-22
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (2.152 Å)
主引用文献Nuclear export receptor CRM1 recognizes diverse conformations in nuclear export signals.
Elife, 6, 2017
1BC0
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BU of 1bc0 by Molmil
RECOMBINANT RAT ANNEXIN V, W185A 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 (2 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
1AWV
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BU of 1awv by Molmil
CYPA COMPLEXED WITH HVGPIA
分子名称: CYCLOPHILIN A, PEPTIDE FROM THE HIV-1 CAPSID PROTEIN
著者Vajdos, F.F.
登録日1997-10-05
公開日1998-03-18
最終更新日2024-05-22
実験手法X-RAY DIFFRACTION (2.34 Å)
主引用文献Crystal structure of cyclophilin A complexed with a binding site peptide from the HIV-1 capsid protein.
Protein Sci., 6, 1997
5VTB
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BU of 5vtb by Molmil
Crystal structure of RBBP4 bound to BCL11a peptide
分子名称: B-cell lymphoma/leukemia 11A, GLYCEROL, Histone-binding protein RBBP4
著者Meagher, J.L, Stuckey, J.A.
登録日2017-05-16
公開日2017-12-27
最終更新日2023-10-04
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Probing the interaction between the histone methyltransferase/deacetylase subunit RBBP4/7 and the transcription factor BCL11A in epigenetic complexes.
J. Biol. Chem., 293, 2018
5TI5
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CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRD4 IN COMPLEX WITH INHIBITOR 8841880
分子名称: 1,2-ETHANEDIOL, 3-bromo-N-[3-(2-oxo-2,3-dihydro-1H-pyrrol-1-yl)phenyl]benzene-1-sulfonamide, Bromodomain-containing protein 4
著者Zhu, J.-Y, Ember, S.W.J, Schonbrunn, E.
登録日2016-10-01
公開日2017-08-09
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (1.83 Å)
主引用文献Identification of a Novel Class of BRD4 Inhibitors by Computational Screening and Binding Simulations.
ACS Omega, 2, 2017
5TI6
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CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRD4 IN COMPLEX WITH INHIBITOR 8841881
分子名称: 1,2-ETHANEDIOL, 2,6-difluoro-N-[3-(2-oxopyrrolidin-1-yl)phenyl]benzene-1-sulfonamide, Bromodomain-containing protein 4
著者Zhu, J.-Y, Ember, S.W.J, Schonbrunn, E.
登録日2016-10-01
公開日2017-08-09
最終更新日2023-10-04
実験手法X-RAY DIFFRACTION (1.704 Å)
主引用文献Identification of a Novel Class of BRD4 Inhibitors by Computational Screening and Binding Simulations.
ACS Omega, 2, 2017
5TI4
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CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRD4 IN COMPLEX WITH INHIBITOR 8841871
分子名称: 1,2-ETHANEDIOL, 3-chloro-4-fluoro-N-[3-(2-oxopyrrolidin-1-yl)phenyl]benzene-1-sulfonamide, Bromodomain-containing protein 4
著者Zhu, J.-Y, Ember, S.W.J, SCHONBRUNN, E.
登録日2016-09-30
公開日2017-08-09
最終更新日2023-10-04
実験手法X-RAY DIFFRACTION (1.62 Å)
主引用文献Identification of a Novel Class of BRD4 Inhibitors by Computational Screening and Binding Simulations.
ACS Omega, 2, 2017
1Z00
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BU of 1z00 by Molmil
Solution structure of the C-terminal domain of ERCC1 complexed with the C-terminal domain of XPF
分子名称: DNA excision repair protein ERCC-1, DNA repair endonuclease XPF
著者Tripsianes, K, Folkers, G, Ab, E, Das, D, Odijk, H, Jaspers, N.G.J, Hoeijmakers, J.H.J, Kaptein, R, Boelens, R.
登録日2005-03-01
公開日2005-12-20
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献The Structure of the Human ERCC1/XPF Interaction Domains Reveals a Complementary Role for the Two Proteins in Nucleotide Excision Repair
Structure, 13, 2005
1ZAI
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BU of 1zai by Molmil
Fructose-1,6-bisphosphate Schiff base intermediate in FBP aldolase from rabbit muscle
分子名称: 1,6-FRUCTOSE DIPHOSPHATE (LINEAR FORM), Fructose-bisphosphate aldolase A
著者St-Jean, M, Lafrance-Vanasse, J, Liotard, B, Sygusch, J.
登録日2005-04-06
公開日2005-05-10
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (1.76 Å)
主引用文献High Resolution Reaction Intermediates of Rabbit Muscle Fructose-1,6-bisphosphate Aldolase: substrate cleavage and induced fit.
J.Biol.Chem., 280, 2005
5T9W
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BU of 5t9w by Molmil
Discovery of a Potent Cyclophilin Inhibitor (Compound 5) based on Structural Simplification of Sanglifehrin A
分子名称: 3-[(3-hydroxyphenyl)methyl]-6-(propan-2-yl)-19-oxa-1,4,7,25-tetraazabicyclo[19.3.1]pentacosa-13,15-diene-2,5,8,20-tetrone, Peptidyl-prolyl cis-trans isomerase A
著者Appleby, T.C, Steadman, V, Pettit, P, Schmitz, U, Mackman, R.L, Schultz, B.
登録日2016-09-09
公開日2017-01-25
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Discovery of Potent Cyclophilin Inhibitors Based on the Structural Simplification of Sanglifehrin A.
J. Med. Chem., 60, 2017
1Z7G
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BU of 1z7g by Molmil
Free human HGPRT
分子名称: Hypoxanthine-guanine phosphoribosyltransferase
著者Keough, D.T, Brereton, I.M, de Jersey, J, Guddat, L.W.
登録日2005-03-24
公開日2005-08-02
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献The Crystal Structure of Free Human Hypoxanthine-guanine Phosphoribosyltransferase Reveals Extensive Conformational Plasticity Throughout the Catalytic Cycle
J.Mol.Biol., 351, 2005
1DOA
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BU of 1doa by Molmil
Structure of the rho family gtp-binding protein cdc42 in complex with the multifunctional regulator rhogdi
分子名称: GERAN-8-YL GERAN, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ...
著者Hoffman, G.R, Nassar, N, Cerione, R.C.
登録日1999-12-20
公開日2000-02-09
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Structure of the Rho family GTP-binding protein Cdc42 in complex with the multifunctional regulator RhoGDI.
Cell(Cambridge,Mass.), 100, 2000
1ZAJ
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BU of 1zaj by Molmil
Fructose-1,6-bisphosphate aldolase from rabbit muscle in complex with mannitol-1,6-bisphosphate, a competitive inhibitor
分子名称: D-MANNITOL-1,6-DIPHOSPHATE, Fructose-bisphosphate aldolase A
著者St-Jean, M, Lafrance-Vanasse, J, Liotard, B, Sygusch, J.
登録日2005-04-06
公開日2005-05-10
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (1.89 Å)
主引用文献High Resolution Reaction Intermediates of Rabbit Muscle Fructose-1,6-bisphosphate Aldolase: substrate cleavage and induced fit.
J.Biol.Chem., 280, 2005
5VOM
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BU of 5vom by Molmil
Benzopiperazine BET bromodomain inhibitor in complex with BD1 of Brd4
分子名称: 3-[(2S)-1-acetyl-4-(furan-2-carbonyl)-2-methyl-1,2,3,4-tetrahydroquinoxalin-6-yl]-N-methylbenzamide, Bromodomain-containing protein 4
著者Toms, A.V, Herbertz, T.
登録日2017-05-03
公開日2017-08-02
最終更新日2024-03-13
実験手法X-RAY DIFFRACTION (1.67 Å)
主引用文献Design and Optimization of Benzopiperazines as Potent Inhibitors of BET Bromodomains.
ACS Med Chem Lett, 8, 2017
2AD9
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BU of 2ad9 by Molmil
Solution structure of Polypyrimidine Tract Binding protein RBD1 complexed with CUCUCU RNA
分子名称: 5'-R(*CP*UP*CP*UP*CP*U)-3', Polypyrimidine tract-binding protein 1
著者Oberstrass, F.C, Auweter, S.D, Erat, M, Hargous, Y, Henning, A, Wenter, P, Reymond, L, Pitsch, S, Black, D.L, Allain, F.H.T.
登録日2005-07-20
公開日2005-10-04
最終更新日2024-05-29
実験手法SOLUTION NMR
主引用文献Structure of PTB bound to RNA: specific binding and implications for splicing regulation
Science, 309, 2005
1E32
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Structure of the N-Terminal domain and the D1 AAA domain of membrane fusion ATPase p97
分子名称: ADENOSINE-5'-DIPHOSPHATE, P97
著者Zhang, X, Shaw, A, Bates, P.A, Gorman, M.A, Kondo, H, Dokurno, P, Leonard M, G, Sternberg, J.E, Freemont, P.S.
登録日2000-06-05
公開日2001-05-31
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Structure of the Aaa ATPase P97
Mol.Cell, 6, 2000
1DT9
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THE CRYSTAL STRUCTURE OF HUMAN EUKARYOTIC RELEASE FACTOR ERF1-MECHANISM OF STOP CODON RECOGNITION AND PEPTIDYL-TRNA HYDROLYSIS
分子名称: PROTEIN (EUKARYOTIC PEPTIDE CHAIN RELEASE FACTOR SUBUNIT 1)
著者Frolova, L.
登録日2000-01-12
公開日2000-02-02
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献The crystal structure of human eukaryotic release factor eRF1--mechanism of stop codon recognition and peptidyl-tRNA hydrolysis.
Cell(Cambridge,Mass.), 100, 2000
1ZAL
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BU of 1zal by Molmil
Fructose-1,6-bisphosphate aldolase from rabbit muscle in complex with partially disordered tagatose-1,6-bisphosphate, a weak competitive inhibitor
分子名称: Fructose-bisphosphate aldolase A, PHOSPHATE ION
著者St-Jean, M, Lafrance-Vanasse, J, Liotard, B, Sygusch, J.
登録日2005-04-06
公開日2005-05-10
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (1.89 Å)
主引用文献High Resolution Reaction Intermediates of Rabbit Muscle Fructose-1,6-bisphosphate Aldolase: substrate cleavage and induced fit.
J.Biol.Chem., 280, 2005
1B64
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SOLUTION STRUCTURE OF THE GUANINE NUCLEOTIDE EXCHANGE FACTOR DOMAIN FROM HUMAN ELONGATION FACTOR-ONE BETA, NMR, 20 STRUCTURES
分子名称: ELONGATION FACTOR 1-BETA
著者Perez, J.M.J, Siegal, G, Kriek, J, Hard, K, Dijk, J, Canters, G.W, Moller, W.
登録日1999-01-20
公開日1999-05-18
最終更新日2024-05-22
実験手法SOLUTION NMR
主引用文献The solution structure of the guanine nucleotide exchange domain of human elongation factor 1beta reveals a striking resemblance to that of EF-Ts from Escherichia coli.
Structure Fold.Des., 7, 1999
1ZKK
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Crystal structure of hSET8 in ternary complex with H4 peptide (16-24) and AdoHcy
分子名称: Histone-lysine N-methyltransferase, H4 lysine-20 specific, Peptide corresponding to residues 15-24 of histone H4, ...
著者Couture, J.-F, Collazo, E, Brunzelle, J.S, Trievel, R.C.
登録日2005-05-03
公開日2005-06-07
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.45 Å)
主引用文献Structural and functional analysis of SET8, a histone H4 Lys-20 methyltransferase
Genes Dev., 19, 2005
1BFS
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BU of 1bfs by Molmil
STRUCTURE OF NF-KB P50 HOMODIMER BOUND TO A KB SITE
分子名称: NUCLEAR FACTOR NF-KAPPA-B P50
著者Huang, D.B, Huxford, T, Chen, Y.Q, Ghosh, G.
登録日1997-09-12
公開日1998-01-28
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献The role of DNA in the mechanism of NFkappaB dimer formation: crystal structures of the dimerization domains of the p50 and p65 subunits.
Structure, 5, 1997

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