6IY0
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![BU of 6iy0 by Molmil](/molmil-images/mine/6iy0) | |
8I33
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5V7I
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![BU of 5v7i by Molmil](/molmil-images/mine/5v7i) | Crystal structure of homo sapiens serine hydroxymethyltransferase 2 (mitochondrial) (SHMT2), in complex with glycine, PLP and folate-competitive pyrazolopyran inhibitor: 6-amino-4-isopropyl-3-methyl-4-(3-(pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile | Descriptor: | (4R)-6-amino-3-methyl-4-(propan-2-yl)-4-[3-(pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl]-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile, DI(HYDROXYETHYL)ETHER, GLYCEROL, ... | Authors: | Ducker, G.S, Ghergurovich, J.M, Mainolfi, N, Suri, V, Jeong, S, Friedman, A, Manfredi, M, Kim, H, Rabinowitz, J.D. | Deposit date: | 2017-03-20 | Release date: | 2017-10-11 | Last modified: | 2023-11-15 | Method: | X-RAY DIFFRACTION (2.47 Å) | Cite: | Human SHMT inhibitors reveal defective glycine import as a targetable metabolic vulnerability of diffuse large B-cell lymphoma. Proc. Natl. Acad. Sci. U.S.A., 114, 2017
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2DUV
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![BU of 2duv by Molmil](/molmil-images/mine/2duv) | Structure of CDK2 with a 3-hydroxychromones | Descriptor: | 2-(3,4-DIHYDROXYPHENYL)-8-(1,1-DIOXIDOISOTHIAZOLIDIN-2-YL)-3-HYDROXY-6-METHYL-4H-CHROMEN-4-ONE, Cell division protein kinase 2 | Authors: | Kim, K.H, Lee, J, Park, T, Jeong, S, Hong, C. | Deposit date: | 2006-07-27 | Release date: | 2007-01-27 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (2.2 Å) | Cite: | 3-Hydroxychromones as cyclin-dependent kinase inhibitors: synthesis and biological evaluation. Bioorg.Med.Chem.Lett., 17, 2007
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5ZNX
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![BU of 5znx by Molmil](/molmil-images/mine/5znx) | Crystal structure of CM14-treated HlyU from Vibrio vulnificus | Descriptor: | Transcriptional activator | Authors: | Park, N, Kim, S, Jo, I, Ahn, J, Hong, S, Jeong, S, Baek, Y. | Deposit date: | 2018-04-11 | Release date: | 2019-04-10 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (2.114 Å) | Cite: | Small-molecule inhibitor of HlyU attenuates virulence of Vibrio species. Sci Rep, 9, 2019
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2R64
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![BU of 2r64 by Molmil](/molmil-images/mine/2r64) | Crystal structure of a 3-aminoindazole compound with CDK2 | Descriptor: | Cell division protein kinase 2, N-[5-(1,1-DIOXIDOISOTHIAZOLIDIN-2-YL)-1H-INDAZOL-3-YL]-2-(4-PIPERIDIN-1-YLPHENYL)ACETAMIDE | Authors: | Lee, J, Choi, H, Kim, K.H, Jeong, S, Park, J.W, Baek, C.S, Lee, S.H. | Deposit date: | 2007-09-05 | Release date: | 2008-09-09 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (2.3 Å) | Cite: | Synthesis and biological evaluation of 3,5-diaminoindazoles as cyclin-dependent kinase inhibitors. Bioorg.Med.Chem.Lett., 18, 2008
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3S2P
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![BU of 3s2p by Molmil](/molmil-images/mine/3s2p) | Crystal structure of CDK2 with a 2-aminopyrimidine compound | Descriptor: | (3S,4S)-1-{3-[2-amino-6-(propan-2-yl)pyrimidin-4-yl]-4-hydroxyphenyl}pyrrolidine-3,4-diol, Cyclin-dependent kinase 2 | Authors: | Kim, K.-H, Lee, J, Jeong, S. | Deposit date: | 2011-05-17 | Release date: | 2011-07-20 | Last modified: | 2024-03-20 | Method: | X-RAY DIFFRACTION (2.3 Å) | Cite: | Discovery of a novel class of 2-aminopyrimidines as CDK1 and CDK2 inhibitors Bioorg.Med.Chem.Lett., 21, 2011
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6KUI
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6KWW
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![BU of 6kww by Molmil](/molmil-images/mine/6kww) | HslU from Staphylococcus aureus | Descriptor: | ATP-dependent protease ATPase subunit HslU | Authors: | Ha, N.-C, Jeong, S. | Deposit date: | 2019-09-09 | Release date: | 2020-07-15 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (3 Å) | Cite: | Cleavage-Dependent Activation of ATP-Dependent Protease HslUV from Staphylococcus aureus . Mol.Cells, 43, 2020
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6KR1
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![BU of 6kr1 by Molmil](/molmil-images/mine/6kr1) | ATP dependent protease HslV from Staphylococcus aureus | Descriptor: | ATP-dependent protease subunit HslV, SULFATE ION | Authors: | Ha, N.-C, Jeong, S. | Deposit date: | 2019-08-20 | Release date: | 2020-07-15 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (2 Å) | Cite: | Cleavage-Dependent Activation of ATP-Dependent Protease HslUV from Staphylococcus aureus . Mol.Cells, 43, 2020
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7CT9
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![BU of 7ct9 by Molmil](/molmil-images/mine/7ct9) | Crystal structure of SAH bound CmoB from Vibrio Vulnificus | Descriptor: | MALONATE ION, PHOSPHATE ION, S-ADENOSYL-L-HOMOCYSTEINE, ... | Authors: | Kim, J, Jeong, S. | Deposit date: | 2020-08-18 | Release date: | 2021-03-03 | Last modified: | 2023-11-29 | Method: | X-RAY DIFFRACTION (2.3 Å) | Cite: | Structural snapshots of CmoB in various states during wobble uridine modification of tRNA. Biochem.Biophys.Res.Commun., 534, 2021
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7CT8
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![BU of 7ct8 by Molmil](/molmil-images/mine/7ct8) | Crystal structure of apo CmoB from Vibrio Vulnificus | Descriptor: | tRNA U34 carboxymethyltransferase | Authors: | Kim, J, Jeong, S. | Deposit date: | 2020-08-18 | Release date: | 2021-03-03 | Last modified: | 2023-11-29 | Method: | X-RAY DIFFRACTION (2.1 Å) | Cite: | Structural snapshots of CmoB in various states during wobble uridine modification of tRNA. Biochem.Biophys.Res.Commun., 534, 2021
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7CTA
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![BU of 7cta by Molmil](/molmil-images/mine/7cta) | Crystal structure of Cx-SAM bound CmoB from Vibrio vulnificus | Descriptor: | (2S)-4-[{[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}(carboxylatomethyl)sulfonio] -2-ammoniobutanoate, SULFATE ION, tRNA U34 carboxymethyltransferase | Authors: | Kim, J, Jeong, S. | Deposit date: | 2020-08-18 | Release date: | 2021-03-03 | Last modified: | 2023-11-29 | Method: | X-RAY DIFFRACTION (2.9 Å) | Cite: | Structural snapshots of CmoB in various states during wobble uridine modification of tRNA. Biochem.Biophys.Res.Commun., 534, 2021
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