1R59
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![BU of 1r59 by Molmil](/molmil-images/mine/1r59) | Enterococcus casseliflavus glycerol kinase | Descriptor: | Glycerol kinase | Authors: | Yeh, J.I, Charrier, V, Paulo, J, Hou, L, Darbon, E, Claiborne, A, Hol, W.G, Deutscher, J. | Deposit date: | 2003-10-09 | Release date: | 2004-10-12 | Last modified: | 2024-02-14 | Method: | X-RAY DIFFRACTION (2.5 Å) | Cite: | Structures of Enterococcal Glycerol Kinase in the Absence and Presence of Glycerol: Correlation of conformation to substrate binding and a mechanism of activation by phosphorylation Biochemistry, 43, 2004
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4EQX
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![BU of 4eqx by Molmil](/molmil-images/mine/4eqx) | Crystal Structure of the C43S Mutant of Staphylococcus aureus CoADR | Descriptor: | CHLORIDE ION, Coenzyme A disulfide reductase, FLAVIN-ADENINE DINUCLEOTIDE, ... | Authors: | Edwards, J.S, Wallace, B.D, Wallen, J.R, Claiborne, A, Redinbo, M.R. | Deposit date: | 2012-04-19 | Release date: | 2012-10-17 | Last modified: | 2024-02-28 | Method: | X-RAY DIFFRACTION (1.7 Å) | Cite: | Turnover-Dependent Covalent Inactivation of Staphylococcus aureus Coenzyme A-Disulfide Reductase by Coenzyme A-Mimetics: Mechanistic and Structural Insights. Biochemistry, 51, 2012
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4EMW
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![BU of 4emw by Molmil](/molmil-images/mine/4emw) | Crystal Structure of Staphylococcus aureus bound with the covalent inhibitor EtVC-CoA | Descriptor: | CHLORIDE ION, Coenzyme A disulfide reductase, FLAVIN-ADENINE DINUCLEOTIDE, ... | Authors: | Edwards, J.S, Wallace, B.D, Claiborne, A, Redinbo, M.R. | Deposit date: | 2012-04-12 | Release date: | 2012-10-17 | Last modified: | 2019-07-17 | Method: | X-RAY DIFFRACTION (2.39 Å) | Cite: | Turnover-Dependent Covalent Inactivation of Staphylococcus aureus Coenzyme A-Disulfide Reductase by Coenzyme A-Mimetics: Mechanistic and Structural Insights. Biochemistry, 51, 2012
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4EQR
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![BU of 4eqr by Molmil](/molmil-images/mine/4eqr) | Crystal structure of the Y361F mutant of Staphylococcus aureus CoADR | Descriptor: | CHLORIDE ION, COENZYME A, Coenzyme A disulfide reductase, ... | Authors: | Wallace, B.D, Edwards, J.S, Wallen, J.R, Claiborne, A, Redinbo, M.R. | Deposit date: | 2012-04-19 | Release date: | 2012-10-17 | Method: | X-RAY DIFFRACTION (1.8 Å) | Cite: | Turnover-Dependent Covalent Inactivation of Staphylococcus aureus Coenzyme A-Disulfide Reductase by Coenzyme A-Mimetics: Mechanistic and Structural Insights. Biochemistry, 51, 2012
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4EQW
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![BU of 4eqw by Molmil](/molmil-images/mine/4eqw) | Crystal Structure of the Y361F, Y419F Mutant of Staphylococcus aureus CoADR | Descriptor: | CHLORIDE ION, COENZYME A, Coenzyme A disulfide reductase, ... | Authors: | Edwards, J.S, Wallace, B.D, Wallen, J.R, Claiborne, A, Redinbo, M.R. | Deposit date: | 2012-04-19 | Release date: | 2012-10-17 | Method: | X-RAY DIFFRACTION (1.5 Å) | Cite: | Turnover-Dependent Covalent Inactivation of Staphylococcus aureus Coenzyme A-Disulfide Reductase by Coenzyme A-Mimetics: Mechanistic and Structural Insights. Biochemistry, 51, 2012
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4EM3
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![BU of 4em3 by Molmil](/molmil-images/mine/4em3) | Crystal Structure of Staphylococcus aureus bound with the covalent inhibitor MeVS-CoA | Descriptor: | CHLORIDE ION, Coenzyme A disulfide reductase, FLAVIN-ADENINE DINUCLEOTIDE, ... | Authors: | Wallace, B.D, Edwards, J.S, Claiborne, A, Redinbo, M.R. | Deposit date: | 2012-04-11 | Release date: | 2012-10-17 | Last modified: | 2017-11-15 | Method: | X-RAY DIFFRACTION (1.977 Å) | Cite: | Turnover-Dependent Covalent Inactivation of Staphylococcus aureus Coenzyme A-Disulfide Reductase by Coenzyme A-Mimetics: Mechanistic and Structural Insights. Biochemistry, 51, 2012
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4EQS
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![BU of 4eqs by Molmil](/molmil-images/mine/4eqs) | Crystal structure of the Y419F mutant of Staphylococcus aureus CoADR | Descriptor: | CHLORIDE ION, COENZYME A, Coenzyme A disulfide reductase, ... | Authors: | Wallace, B.D, Edwards, J.S, Wallen, J.R, Claiborne, A, Redinbo, M.R. | Deposit date: | 2012-04-19 | Release date: | 2012-10-17 | Method: | X-RAY DIFFRACTION (1.5 Å) | Cite: | Turnover-Dependent Covalent Inactivation of Staphylococcus aureus Coenzyme A-Disulfide Reductase by Coenzyme A-Mimetics: Mechanistic and Structural Insights. Biochemistry, 51, 2012
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4EM4
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![BU of 4em4 by Molmil](/molmil-images/mine/4em4) | Crystal Structure of Staphylococcus aureus bound with the covalent inhibitor Pethyl-VS-CoA | Descriptor: | CHLORIDE ION, Coenzyme A disulfide reductase, FLAVIN-ADENINE DINUCLEOTIDE, ... | Authors: | Wallace, B.D, Edwards, J.S, Claiborne, A, Redinbo, M.R. | Deposit date: | 2012-04-11 | Release date: | 2012-10-17 | Last modified: | 2017-11-15 | Method: | X-RAY DIFFRACTION (1.821 Å) | Cite: | Turnover-Dependent Covalent Inactivation of Staphylococcus aureus Coenzyme A-Disulfide Reductase by Coenzyme A-Mimetics: Mechanistic and Structural Insights. Biochemistry, 51, 2012
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7M6K
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![BU of 7m6k by Molmil](/molmil-images/mine/7m6k) | |
3CGE
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![BU of 3cge by Molmil](/molmil-images/mine/3cge) | |
1JOA
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![BU of 1joa by Molmil](/molmil-images/mine/1joa) | NADH PEROXIDASE WITH CYSTEINE-SULFENIC ACID | Descriptor: | FLAVIN-ADENINE DINUCLEOTIDE, NADH PEROXIDASE | Authors: | Yeh, J.I, Claiborne, A.C, Hol, W.G.J. | Deposit date: | 1996-07-02 | Release date: | 1997-01-11 | Last modified: | 2024-04-03 | Method: | X-RAY DIFFRACTION (2.8 Å) | Cite: | Structure of the native cysteine-sulfenic acid redox center of enterococcal NADH peroxidase refined at 2.8 A resolution. Biochemistry, 35, 1996
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3CGD
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![BU of 3cgd by Molmil](/molmil-images/mine/3cgd) | |
3CGB
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![BU of 3cgb by Molmil](/molmil-images/mine/3cgb) | |
3CGC
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![BU of 3cgc by Molmil](/molmil-images/mine/3cgc) | |
2H3G
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![BU of 2h3g by Molmil](/molmil-images/mine/2h3g) | |
2E9N
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![BU of 2e9n by Molmil](/molmil-images/mine/2e9n) | Structure of h-CHK1 complexed with A767085 | Descriptor: | 3-(4'-HYDROXYBIPHENYL-4-YL)-N-(4-HYDROXYCYCLOHEXYL)-1,4-DIHYDROINDENO[1,2-C]PYRAZOLE-6-CARBOXAMIDE, Serine/threonine-protein kinase Chk1 | Authors: | Park, C. | Deposit date: | 2007-01-26 | Release date: | 2008-01-29 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (2.5 Å) | Cite: | Discovery of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of potent and selective checkpoint kinase 1 inhibitors. Bioorg.Med.Chem., 15, 2007
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1XUP
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![BU of 1xup by Molmil](/molmil-images/mine/1xup) | ENTEROCOCCUS CASSELIFLAVUS GLYCEROL KINASE COMPLEXED WITH GLYCEROL | Descriptor: | GLYCEROL, Glycerol kinase | Authors: | Yeh, J.I, Charrier, V, Paulo, J, Hou, L, Darbon, E, Hol, W.G.J, Deutscher, J. | Deposit date: | 2004-10-26 | Release date: | 2004-12-14 | Last modified: | 2024-02-14 | Method: | X-RAY DIFFRACTION (2.75 Å) | Cite: | Structures of Enterococcal Glycerol Kinase in the Absence and Presence of Glycerol: Correlation of Conformation to Substrate Binding and a Mechanism of Activation by Phosphorylation Biochemistry, 43, 2004
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2E9V
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![BU of 2e9v by Molmil](/molmil-images/mine/2e9v) | Structure of h-CHK1 complexed with A859017 | Descriptor: | 18-CHLORO-2-OXO-17-[(PYRIDIN-4-YLMETHYL)AMINO]-2,3,11,12,13,14-HEXAHYDRO-1H,10H-4,8-(AZENO)-9,15,1,3,6-BENZODIOXATRIAZACYCLOHEPTADECINE-7-CARBONITRILE, Serine/threonine-protein kinase Chk1 | Authors: | Park, C. | Deposit date: | 2007-01-27 | Release date: | 2008-01-29 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (2 Å) | Cite: | Structure-Based Design, Synthesis and Biological Evaluation of Potent Selective Macrocyclic Chk1 Inhibitors To be Published
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2E9O
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![BU of 2e9o by Molmil](/molmil-images/mine/2e9o) | Structure of h-CHK1 complexed with AA582939 | Descriptor: | 4-(6-{[(4-METHYLCYCLOHEXYL)AMINO]METHYL}-1,4-DIHYDROINDENO[1,2-C]PYRAZOL-3-YL)BENZOIC ACID, Serine/threonine-protein kinase Chk1 | Authors: | Park, C. | Deposit date: | 2007-01-26 | Release date: | 2008-01-29 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (2.1 Å) | Cite: | Discovery of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of potent and selective checkpoint kinase 1 inhibitors. Bioorg.Med.Chem., 15, 2007
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2BC0
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![BU of 2bc0 by Molmil](/molmil-images/mine/2bc0) | |
2BCP
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![BU of 2bcp by Molmil](/molmil-images/mine/2bcp) | |
2BC1
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![BU of 2bc1 by Molmil](/molmil-images/mine/2bc1) | |
2E9P
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![BU of 2e9p by Molmil](/molmil-images/mine/2e9p) | Structure of h-CHK1 complexed with A771129 | Descriptor: | 1-(5-CHLORO-2-METHOXYPHENYL)-3-{6-[2-(DIMETHYLAMINO)-1-METHYLETHOXY]PYRAZIN-2-YL}UREA, Serine/threonine-protein kinase Chk1 | Authors: | Park, C. | Deposit date: | 2007-01-26 | Release date: | 2008-01-29 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (2.6 Å) | Cite: | Structure-Based Design, Synthesis and Biological Evaluation of Potent and Selective Macrocyclic Chk1 Inhibitors To be Published
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2E9U
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![BU of 2e9u by Molmil](/molmil-images/mine/2e9u) | Structure of h-CHK1 complexed with A780125 | Descriptor: | 18-CHLORO-11,12,13,14-TETRAHYDRO-1H,10H-8,4-(AZENO)-9,15,1,3,6-BENZODIOXATRIAZACYCLOHEPTADECIN-2-ONE, Serine/threonine-protein kinase Chk1 | Authors: | Park, C. | Deposit date: | 2007-01-27 | Release date: | 2008-01-29 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (2 Å) | Cite: | Structure-Based Design, Synthesis and Biological Evaluation of Potent Selective Macrocyclic Chk1 Inhibitors To be Published
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