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PDB: 102 results

3O63
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Crystal Structure of Thiamin Phosphate Synthase from Mycobacterium tuberculosis
Descriptor: PHOSPHATE ION, Probable thiamine-phosphate pyrophosphorylase
Authors:McCulloch, K.M, Ramamoorthy, D, Ishida, K, Guida, W.C, Begley, T.P, Ealick, S.E.
Deposit date:2010-07-28
Release date:2011-07-27
Last modified:2024-02-21
Method:X-RAY DIFFRACTION (2.35 Å)
Cite:Crystal Structure and Identification of Potential Inhibitor Compounds for Mycobacterium tuberculosis Thiamin Phosphate Synthase
to be published
5YOK
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BU of 5yok by Molmil
Structure of HIV-1 Protease in Complex with Inhibitor KNI-1657
Descriptor: (4R)-N-[(2,6-dimethylphenyl)methyl]-3-[(2S,3S)-3-[[(2S)-2-[(7-methoxy-1-benzofuran-2-yl)carbonylamino]-2-[(3R)-oxolan-3 -yl]ethanoyl]amino]-2-oxidanyl-4-phenyl-butanoyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxamide, GLYCEROL, HIV-1 PROTEASE
Authors:Adachi, M, Hidaka, K, Kuroki, R, Kiso, Y.
Deposit date:2017-10-29
Release date:2018-07-18
Last modified:2024-03-27
Method:X-RAY DIFFRACTION (0.85 Å)
Cite:Identification of Highly Potent Human Immunodeficiency Virus Type-1 Protease Inhibitors against Lopinavir and Darunavir Resistant Viruses from Allophenylnorstatine-Based Peptidomimetics with P2 Tetrahydrofuranylglycine.
J. Med. Chem., 61, 2018
7DU8
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Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with Selpercatinib
Descriptor: Proto-oncogene tyrosine-protein kinase receptor Ret, Selpercatinib
Authors:Miyazaki, I, Ishida, K, Suzuki, T.
Deposit date:2021-01-08
Release date:2022-02-02
Last modified:2024-05-29
Method:X-RAY DIFFRACTION (2.75 Å)
Cite:Selective RET inhibitor TAS0953/HM06
To be published
7DUA
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Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with 4-amino-7-(1-methylcyclopropyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[2,3-d]pyrimidine-5-carboxamide
Descriptor: 4-azanyl-7-(1-methylcyclopropyl)-~{N}-(5-methyl-1~{H}-pyrazol-3-yl)pyrrolo[2,3-d]pyrimidine-5-carboxamide, Proto-oncogene tyrosine-protein kinase receptor Ret
Authors:Miyazaki, I, Ishida, K, Suzuki, T.
Deposit date:2021-01-08
Release date:2022-01-12
Last modified:2024-05-29
Method:X-RAY DIFFRACTION (1.64 Å)
Cite:Selective RET inhibitor TAS0953/HM06
To be published
7DU9
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Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with Pralsetinib
Descriptor: Pralsetinib, Proto-oncogene tyrosine-protein kinase receptor Ret
Authors:Miyazaki, I, Ishida, K, Suzuki, T.
Deposit date:2021-01-08
Release date:2022-01-12
Last modified:2024-05-29
Method:X-RAY DIFFRACTION (2.31 Å)
Cite:Selective RET inhibitor TAS0953/HM06
To be published
3FE0
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BU of 3fe0 by Molmil
X-ray crystal structure of wild type human lysozyme in D2O
Descriptor: Lysozyme C
Authors:Chiba-Kamoshida, K, Matsui, T, Chatake, T, Ohhara, T, Ostermann, A, Tanaka, I, Yutani, K, Niimura, N.
Deposit date:2008-11-27
Release date:2009-12-08
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:Site-specific softening of peptide bonds by localized deuterium observed by neutron crystallography of human lysozyme hydrogen
To be Published
1GTG
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BU of 1gtg by Molmil
Crystal structure of the thermostable serine-carboxyl type proteinase, kumamolysin (kscp)
Descriptor: CALCIUM ION, KUMAMOLYSIN
Authors:Comellas-Bigler, M, Fuentes-Prior, P, Maskos, K, Huber, R, Oyama, H, Uchida, K, Dunn, B.M, Oda, K, Bode, W.
Deposit date:2002-01-15
Release date:2002-06-13
Last modified:2023-12-13
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:The 1.4 A Crystal Structure of Kumamolysin. A Thermostable Serine-Carboxyl-Type Proteinase
Structure, 10, 2002
1GTL
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The thermostable serine-carboxyl type proteinase, kumamolisin (KSCP) - complex with Ac-Ile-Pro-Phe-cho
Descriptor: ALDEHYDE INHIBITOR, CALCIUM ION, KUMAMOLYSIN, ...
Authors:Comellas-Bigler, M, Fuentes-Prior, P, Maskos, K, Huber, R, Oyama, H, Uchida, K, Dunn, B.M, Oda, K, Bode, W.
Deposit date:2002-01-16
Release date:2002-06-13
Last modified:2023-12-13
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:The 1.4 A Crystal Structure of Kumamolysin. A Thermostable Serine-Carboxyl-Type Proteinase
Structure, 10, 2002
1GT9
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High resolution crystal structure of a thermostable serine-carboxyl type proteinase, kumamolisin (kscp)
Descriptor: CALCIUM ION, KUMAMOLYSIN, SULFATE ION
Authors:Comellas-Bigler, M, Fuentes-Prior, P, Maskos, K, Huber, R, Oyama, H, Uchida, K, Dunn, B.M, Oda, K, Bode, W.
Deposit date:2002-01-14
Release date:2002-06-13
Last modified:2023-12-13
Method:X-RAY DIFFRACTION (1.38 Å)
Cite:The 1.4 A Crystal Structure of Kumamolysin. A Thermostable Serine-Carboxyl-Type Proteinase
Structure, 10, 2002
1GTJ
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Crystal structure of the thermostable serine-carboxyl type proteinase, kumamolisin (KSCP) - complex with Ac-Ile-Ala-Phe-cho
Descriptor: ALDEHYDE INHIBITOR, CALCIUM ION, KUMAMOLYSIN, ...
Authors:Comellas-Bigler, M, Fuentes-Prior, P, Maskos, K, Huber, R, Oyama, H, Uchida, K, Dunn, B.M, Oda, K, Bode, W.
Deposit date:2002-01-15
Release date:2002-06-13
Last modified:2023-12-13
Method:X-RAY DIFFRACTION (1.75 Å)
Cite:The 1.4 A Crystal Structure of Kumamolysin. A Thermostable Serine-Carboxyl-Type Proteinase
Structure, 10, 2002
1FGG
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CRYSTAL STRUCTURE OF 1,3-GLUCURONYLTRANSFERASE I (GLCAT-I) COMPLEXED WITH GAL-GAL-XYL, UDP, AND MN2+
Descriptor: GLUCURONYLTRANSFERASE I, MANGANESE (II) ION, UNKNOWN ATOM OR ION, ...
Authors:Pedersen, L.C, Tsuchida, K, Kitagawa, H, Sugahara, K, Darden, T.A.
Deposit date:2000-07-28
Release date:2001-01-31
Last modified:2024-03-13
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Heparan/chondroitin sulfate biosynthesis. Structure and mechanism of human glucuronyltransferase I.
J.Biol.Chem., 275, 2000
3O16
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Crystal Structure of Bacillus subtilis Thiamin Phosphate Synthase K159A
Descriptor: Thiamine-phosphate pyrophosphorylase
Authors:McCulloch, K.M, Hanes, J.W, Abdelwahed, S, Mahanta, N, Hazra, A, Ishida, K, Begley, T.P, Ealick, S.E.
Deposit date:2010-07-20
Release date:2011-07-27
Last modified:2024-02-21
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Crystal Structure and Kinetic Characterization of Bacillus subtilis Thiamin Phosphate Synthase with a Carboxylated Thiazole Phosphate
to be published
1GA4
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BU of 1ga4 by Molmil
CRYSTAL STRUCTURE ANALYSIS OF PSCP (PSEUDOMONAS SERINE-CARBOXYL PROTEINASE) COMPLEXED WITH INHIBITOR PSEUDOIODOTYROSTATIN (THIS ENZYME RENAMED "SEDOLISIN" IN 2003)
Descriptor: CALCIUM ION, GLYCEROL, PSEUDOIODOTYROSTATIN, ...
Authors:Wlodawer, A, Li, M, Dauter, Z, Gustchina, A, Uchida, K.
Deposit date:2000-11-29
Release date:2000-12-13
Last modified:2023-08-09
Method:X-RAY DIFFRACTION (1.4 Å)
Cite:Carboxyl proteinase from Pseudomonas defines a novel family of subtilisin-like enzymes.
Nat.Struct.Biol., 8, 2001
3O15
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Crystal Structure of Bacillus subtilis Thiamin Phosphate Synthase Complexed with a Carboxylated Thiazole Phosphate
Descriptor: 2-TRIFLUOROMETHYL-5-METHYLENE-5H-PYRIMIDIN-4-YLIDENEAMINE, 4-methyl-5-[2-(phosphonooxy)ethyl]-1,3-thiazole-2-carboxylic acid, PYROPHOSPHATE 2-, ...
Authors:McCulloch, K.M, Hanes, J.W, Abdelwahed, S, Mahanta, N, Hazra, A, Ishida, K, Begley, T.P, Ealick, S.E.
Deposit date:2010-07-20
Release date:2011-07-27
Last modified:2024-02-21
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:Crystal Structure and Kinetic Characterization of Bacillus subtilis Thiamin Phosphate Synthase with a Carboxylated Thiazole Phosphate
to be published
1GA6
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BU of 1ga6 by Molmil
CRYSTAL STRUCTURE ANALYSIS OF PSCP (PSEUDOMONAS SERINE-CARBOXYL PROTEINASE) COMPLEXED WITH A FRAGMENT OF TYROSTATIN (THIS ENZYME RENAMED "SEDOLISIN" IN 2003)
Descriptor: ACETATE ION, CALCIUM ION, FRAGMENT OF TYROSTATIN, ...
Authors:Wlodawer, A, Li, M, Dauter, Z, Gustchina, A, Uchida, K.
Deposit date:2000-11-29
Release date:2000-12-13
Last modified:2023-08-09
Method:X-RAY DIFFRACTION (1 Å)
Cite:Carboxyl proteinase from Pseudomonas defines a novel family of subtilisin-like enzymes.
Nat.Struct.Biol., 8, 2001
4ZD3
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Structure of a transglutaminase 2-specific autoantibody Fab fragment
Descriptor: 679-14-14E06 Fab fragment heavy chain, 679-14-14E06 Fab fragment light chain
Authors:Chen, X, Dalhus, B, Hnida, K, Iversen, R, Sollid, L.M.
Deposit date:2015-04-16
Release date:2015-07-22
Last modified:2024-01-10
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Structural Basis for Antigen Recognition by Transglutaminase 2-specific Autoantibodies in Celiac Disease.
J.Biol.Chem., 290, 2015
2Z7W
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BU of 2z7w by Molmil
Crystal Structure of H2O2 treated Cu,Zn-SOD
Descriptor: COPPER (II) ION, Superoxide dismutase [Cu-Zn], ZINC ION
Authors:Ito, S, Ishii, T, Uchida, K.
Deposit date:2007-08-29
Release date:2008-09-02
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Crystal structures of H2O2-treated Cu,Zn-superoxide dismutase
To be Published
2Z7U
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BU of 2z7u by Molmil
Crystal Structure of H2O2 treated Cu,Zn-SOD
Descriptor: COPPER (II) ION, Superoxide dismutase [Cu-Zn], ZINC ION
Authors:Ito, S, Ishii, T, Uchida, K.
Deposit date:2007-08-28
Release date:2008-09-02
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Crystal structures of H2O2-treated Cu,Zn-superoxide dismutase
To be Published
3RQW
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Crystal structure of acetylcholine bound to a prokaryotic pentameric ligand-gated ion channel, ELIC
Descriptor: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, ACETYLCHOLINE, ELIC Pentameric Ligand Gated Ion Channel from Erwinia Chrysanthemi, ...
Authors:Pan, J.J, Chen, Q, Yoshida, K, Cohen, A, Kong, X.P, Xu, Y, Tang, P.
Deposit date:2011-04-28
Release date:2012-03-07
Last modified:2023-09-13
Method:X-RAY DIFFRACTION (2.913 Å)
Cite:Structure of the pentameric ligand-gated ion channel ELIC cocrystallized with its competitive antagonist acetylcholine.
Nat Commun, 3, 2012
2Z7Y
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BU of 2z7y by Molmil
Crystal Structure of H2O2 treated Cu,Zn-SOD
Descriptor: COPPER (II) ION, Superoxide dismutase [Cu-Zn], ZINC ION
Authors:Ito, S, Ishii, T, Uchida, K.
Deposit date:2007-08-30
Release date:2008-09-02
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (1.55 Å)
Cite:Crystal structure of H2O2-treated Cu,Zn-superoxide dismutase
To be Published
2ZOW
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BU of 2zow by Molmil
Crystal Structure of H2O2 treated Cu,Zn-SOD
Descriptor: COPPER (I) ION, Superoxide dismutase [Cu-Zn], ZINC ION
Authors:Ito, S, Ishii, T, Sakai, H, Uchida, K.
Deposit date:2008-06-11
Release date:2009-06-30
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (1.45 Å)
Cite:Crystal structures of H2O2-treated Cu,Zn-superoxide dismutase
To be Published
2Z7Z
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BU of 2z7z by Molmil
Crystal Structure of H2O2 treated Cu,Zn-SOD
Descriptor: COPPER (II) ION, Superoxide dismutase [Cu-Zn], ZINC ION
Authors:Ito, S, Ishii, T, Uchida, K.
Deposit date:2007-08-30
Release date:2008-09-02
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (1.85 Å)
Cite:Crystal structure of H2O2-treated Cu,Zn-superoxide dismutase
To be Published
3RQU
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Crystal structure of a prokaryotic pentameric ligand-gated ion channel, ELIC
Descriptor: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, ELIC Pentameric Ligand Gated Ion Channel from Erwinia Chrysanthemi, GLYCEROL
Authors:Pan, J.J, Chen, Q, Yoshida, K, Cohen, A, Kong, X.P, Xu, Y, Tang, P.
Deposit date:2011-04-28
Release date:2012-03-07
Last modified:2023-09-13
Method:X-RAY DIFFRACTION (3.089 Å)
Cite:Structure of the pentameric ligand-gated ion channel ELIC cocrystallized with its competitive antagonist acetylcholine.
Nat Commun, 3, 2012
2E1Q
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Crystal Structure of Human Xanthine Oxidoreductase mutant, Glu803Val
Descriptor: 2-HYDROXYBENZOIC ACID, BICARBONATE ION, CALCIUM ION, ...
Authors:Yamaguchi, Y, Matsumura, T, Ichida, K, Okamoto, K, Nishino, T.
Deposit date:2006-10-27
Release date:2007-09-18
Last modified:2023-10-25
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Human xanthine oxidase changes its substrate specificity to aldehyde oxidase type upon mutation of amino acid residues in the active site: roles of active site residues in binding and activation of purine substrate
J.Biochem.(Tokyo), 141, 2007
3A2O
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Crystal Structure of HIV-1 Protease Complexed with KNI-1689
Descriptor: (4R)-3-[(2S,3S)-3-{[(4-amino-2,6-dimethylphenoxy)acetyl]amino}-2-hydroxy-4-phenylbutanoyl]-5,5-dimethyl-N-(2-methylprop -2-en-1-yl)-1,3-thiazolidine-4-carboxamide, GLYCEROL, PROTEASE
Authors:Adachi, M, Tamada, T, Hidaka, K, Kimura, T, Kiso, Y, Kuroki, R.
Deposit date:2009-05-26
Release date:2010-03-02
Last modified:2024-05-29
Method:X-RAY DIFFRACTION (0.88 Å)
Cite:Small-sized human immunodeficiency virus type-1 protease inhibitors containing allophenylnorstatine to explore the S2' pocket.
J.Med.Chem., 52, 2009

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