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PDB: 11 results

3I6O
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Crystal structure of wild type HIV-1 protease with macrocyclic inhibitor GRL-0216A
Descriptor: (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl {(1S,2R)-1-benzyl-2-hydroxy-3-[(7E)-13-methoxy-1,1-dioxido-3,4,5,6,9,10-hexahydro-2H-11,1,2-benzoxathiazacyclotridecin-2-yl]propyl}carbamate, GLYCEROL, IODIDE ION, ...
Authors:Chumanevich, A.A, Wang, Y.-F, Kovalevsky, A.Y, Weber, I.T.
Deposit date:2009-07-07
Release date:2009-09-29
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.17 Å)
Cite:Design, Synthesis, Protein-Ligand X-ray Structure, and Biological Evaluation of a Series of Novel Macrocyclic Human Immunodeficiency Virus-1 Protease Inhibitors to Combat Drug Resistance.
J.Med.Chem., 52, 2009
3B80
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HIV-1 protease mutant I54V complexed with gem-diol-amine intermediate NLLTQI
Descriptor: CHLORIDE ION, Protease, SODIUM ION, ...
Authors:Chumanevich, A.A, Kovalevsky, A.Y, Weber, I.T.
Deposit date:2007-10-31
Release date:2007-12-18
Last modified:2023-08-30
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:Caught in the Act: The 1.5 A Resolution Crystal Structures of the HIV-1 Protease and the I54V Mutant Reveal a Tetrahedral Reaction Intermediate.
Biochemistry, 46, 2007
1S3I
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Crystal structure of the N terminal hydrolase domain of 10-formyltetrahydrofolate dehydrogenase
Descriptor: 10-formyltetrahydrofolate dehydrogenase, BETA-MERCAPTOETHANOL
Authors:Chumanevich, A.A, Krupenko, S.A, Davies, C.
Deposit date:2004-01-13
Release date:2004-01-27
Last modified:2021-10-27
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:The crystal structure of the hydrolase domain of 10-formyltetrahydrofolate dehydrogenase: mechanism of hydrolysis and its interplay with the dehydrogenase domain.
J.Biol.Chem., 279, 2004
3AMI
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The crystal structure of the M16B metallopeptidase subunit from Sphingomonas sp. A1
Descriptor: zinc peptidase
Authors:Maruyama, Y, Chuma, A, Mikami, B, Hashimoto, W, Murata, K.
Deposit date:2010-08-20
Release date:2011-02-02
Last modified:2024-03-13
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Heterosubunit composition and crystal structures of a novel bacterial M16B metallopeptidase
J.Mol.Biol., 407, 2011
3AMJ
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The crystal structure of the heterodimer of M16B peptidase from Sphingomonas sp. A1
Descriptor: ZINC ION, zinc peptidase active subunit, zinc peptidase inactive subunit
Authors:Maruyama, Y, Chuma, A, Mikami, B, Hashimoto, W, Murata, K.
Deposit date:2010-08-20
Release date:2011-02-09
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (3 Å)
Cite:Heterosubunit composition and crystal structures of a novel bacterial M16B metallopeptidase
J.Mol.Biol., 407, 2011
3B7V
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HIV-1 protease complexed with gem-diol-amine tetrahedral intermediate NLLTQI
Descriptor: CHLORIDE ION, GLYCEROL, Protease, ...
Authors:Kovalevsky, A.Y, Chumanevich, A.A, Weber, I.T.
Deposit date:2007-10-31
Release date:2007-12-18
Last modified:2023-08-30
Method:X-RAY DIFFRACTION (1.46 Å)
Cite:Caught in the Act: The 1.5 A Resolution Crystal Structures of the HIV-1 Protease and the I54V Mutant Reveal a Tetrahedral Reaction Intermediate.
Biochemistry, 46, 2007
3B1U
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Crystal structure of human peptidylarginine deiminase 4 in complex with o-F-amidine
Descriptor: 2-{[(2S)-1-amino-5-{[(1Z)-2-fluoroethanimidoyl]amino}-1-oxopentan-2-yl]carbamoyl}benzoic acid, CALCIUM ION, Protein-arginine deiminase type-4, ...
Authors:Causey, C.P, Jones, J.E, Slack, J.L, Kamei, D, Jones Jr, L.E, Subramanian, V, Knuckley, B, Ebrahimi, P, Chumanevich, A.A, Luo, Y, Hashimoto, H, Shimizu, T, Sato, M, Hofseth, L.J, Thompson, P.R.
Deposit date:2011-07-13
Release date:2011-10-26
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:The Development of N-alpha-(2-Carboxyl)benzoyl-N(5)-(2-fluoro-1-iminoethyl)-l-ornithine Amide (o-F-amidine) and N-alpha-(2-Carboxyl)benzoyl-N(5)-(2-chloro-1-iminoethyl)-l-ornithine Amide (o-Cl-amidine) As Second Generation Protein Arginine Deiminase (PAD) Inhibitors
J.Med.Chem., 54, 2011
3B1T
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BU of 3b1t by Molmil
Crystal structure of human peptidylarginine deiminase 4 in complex with o-Cl-amidine
Descriptor: 2-{[(2S)-1-amino-5-{[(1Z)-2-chloroethanimidoyl]amino}-1-oxopentan-2-yl]carbamoyl}benzoic acid, CALCIUM ION, Protein-arginine deiminase type-4, ...
Authors:Causey, C.P, Jones, J.E, Slack, J.L, Kamei, D, Jones Jr, L.E, Subramanian, V, Knuckley, B, Ebrahimi, P, Chumanevich, A.A, Luo, Y, Hashimoto, H, Shimizu, T, Sato, M, Hofseth, L.J, Thompson, P.R.
Deposit date:2011-07-13
Release date:2011-10-26
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:The Development of N-alpha-(2-Carboxyl)benzoyl-N(5)-(2-fluoro-1-iminoethyl)-l-ornithine Amide (o-F-amidine) and N-alpha-(2-Carboxyl)benzoyl-N(5)-(2-chloro-1-iminoethyl)-l-ornithine Amide (o-Cl-amidine) As Second Generation Protein Arginine Deiminase (PAD) Inhibitors
J.Med.Chem., 54, 2011
1F6L
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VARIABLE LIGHT CHAIN DIMER OF ANTI-FERRITIN ANTIBODY
Descriptor: ANTI-FERRITIN IMMUNOGLOBULIN LIGHT CHAIN
Authors:Nymalm, Y, Kravchuk, Z, Salminen, T, Chumanevich, A.A, Dubnovitsky, A.P, Kankare, J, Pentikainen, O, Lehtonen, J, Arosio, P, Martsev, S, Johnson, M.S.
Deposit date:2000-06-22
Release date:2002-10-23
Last modified:2018-04-04
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Antiferritin VL homodimer binds human spleen ferritin with high specificity
J.STRUCT.BIOL., 138, 2002
3GUB
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Crystal structure of DAPKL93G complexed with N6-(2-Phenylethyl)adenosine
Descriptor: 9-alpha-L-lyxofuranosyl-N-(2-phenylethyl)-9H-purin-6-amine, Death-associated protein kinase 1, SULFATE ION
Authors:McNamara, L.K, Schumacher, A.M, Schavocky, J.S, Watterson, D.M, Brunzelle, J.S.
Deposit date:2009-03-29
Release date:2010-03-09
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.71 Å)
Cite:Crystal structures of the DAPK gatekeeper mutant complexed with N6-modified adenosine analogs.
To be Published
3GU8
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Crystal structure of DAPKL93G with N6-cyclopentyladenosine
Descriptor: Death-associated protein kinase 1, N6-cyclopentyladenosine
Authors:McNamara, L.K, Schumacher, A.M, Schavocky, J.S, Watterson, D.M, Brunzelle, J.S.
Deposit date:2009-03-28
Release date:2010-03-09
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.6 Å)
Cite:Crystal structures of the DAPK gatekeeper mutant with N6-modified adenosine analogs.
To be Published

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