8Q3S
 
 | HsNMT1 in complex with both MyrCoA and GNCFSKAR inhibitor peptide | 分子名称: | CHLORIDE ION, COENZYME A, GLY-ASN-CYS-PHE-SER-LYS-ALA-ARG, ... | 著者 | Dian, C, Giglione, C, Meinnel, T. | 登録日 | 2023-08-04 | 公開日 | 2024-08-14 | 最終更新日 | 2025-02-26 | 実験手法 | X-RAY DIFFRACTION (1.78 Å) | 主引用文献 | Novel, tightly structurally related N-myristoyltransferase inhibitors display equally potent yet distinct inhibitory mechanisms. Structure, 32, 2024
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8Q23
 
 | HsNMT1 in complex with both MyrCoA and Ac-D-ORN-SFSKPR inhibitor peptide | 分子名称: | ACE-ORD-SER-PHE-SER-LYS-PRO-ARG, CHLORIDE ION, GLYCEROL, ... | 著者 | Dian, C, Giglione, C, Meinnel, T. | 登録日 | 2023-08-01 | 公開日 | 2024-08-14 | 最終更新日 | 2025-02-26 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Novel, tightly structurally related N-myristoyltransferase inhibitors display equally potent yet distinct inhibitory mechanisms. Structure, 32, 2024
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8Q3T
 
 | HsNMT1 in complex with both MyrCoA and GNCFSKPRVPTK inhibitor peptide | 分子名称: | CHLORIDE ION, COENZYME A, GLYCEROL, ... | 著者 | Dian, C, Giglione, C, Meinnel, T. | 登録日 | 2023-08-04 | 公開日 | 2024-08-14 | 最終更新日 | 2025-02-26 | 実験手法 | X-RAY DIFFRACTION (1.96 Å) | 主引用文献 | Novel, tightly structurally related N-myristoyltransferase inhibitors display equally potent yet distinct inhibitory mechanisms. Structure, 32, 2024
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8Q2Z
 
 | HsNMT1 in complex with both MyrCoA and GNLLSKFR peptide | 分子名称: | CHLORIDE ION, COENZYME A, GLYCEROL, ... | 著者 | Dian, C, Giglione, C, Meinnel, T. | 登録日 | 2023-08-03 | 公開日 | 2024-08-14 | 最終更新日 | 2025-02-26 | 実験手法 | X-RAY DIFFRACTION (1.88 Å) | 主引用文献 | Novel, tightly structurally related N-myristoyltransferase inhibitors display equally potent yet distinct inhibitory mechanisms. Structure, 32, 2024
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8Q24
 
 | HsNMT1 in complex with both MyrCoA and (DAB)SFSKPR inhibitor peptide | 分子名称: | CHLORIDE ION, DAB-SER-PHE-SER-LYS-PRO-ARG, GLYCEROL, ... | 著者 | Dian, C, Giglione, C, Meinnel, T. | 登録日 | 2023-08-01 | 公開日 | 2024-08-14 | 最終更新日 | 2025-02-26 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Novel, tightly structurally related N-myristoyltransferase inhibitors display equally potent yet distinct inhibitory mechanisms. Structure, 32, 2024
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3IQS
 
 | Crystal structure of the anti-viral APOBEC3G catalytic domain | 分子名称: | DNA dC->dU-editing enzyme APOBEC-3G, ZINC ION | 著者 | Holden, L.G, Prochnow, C, Chang, Y.P, Bransteitter, R, Chelico, L, Sen, U, Stevens, R.C, Goodman, R.F, Chen, X.S. | 登録日 | 2009-08-20 | 公開日 | 2009-11-10 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Crystal structure of the anti-viral APOBEC3G catalytic domain and functional implications. Nature, 456, 2008
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8QUS
 
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8QU7
 
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8QOC
 
 | Crystal structure of Staphylococcus aureus PLP Synthase (Pdx1) | 分子名称: | 1,2-ETHANEDIOL, CHLORIDE ION, MAGNESIUM ION, ... | 著者 | Ullah, N, Wrenger, C, Betzel, C. | 登録日 | 2023-09-28 | 公開日 | 2024-10-02 | 実験手法 | X-RAY DIFFRACTION (2.83 Å) | 主引用文献 | Structure and dynamics of the staphylococcal pyridoxal 5-phosphate synthase complex reveal transient interactions at the enzyme interface. J.Biol.Chem., 300, 2024
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8R1M
 
 | Structure of TxGH116 with covalently bound N-azido-octyl aziridine | 分子名称: | (1R,2R,3R,4S)-4-[8-(azanyldiazenyl)octylamino]-3-(hydroxymethyl)cyclopentane-1,2-diol, CALCIUM ION, CHLORIDE ION, ... | 著者 | Offen, W.A, Davies, G.J. | 登録日 | 2023-11-02 | 公開日 | 2024-10-02 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Selective labelling of GBA2 in cells with fluorescent beta-d-arabinofuranosyl cyclitol aziridines. Chem Sci, 15, 2024
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8QAT
 
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8QQL
 
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1XEK
 
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1XEI
 
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1XEJ
 
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1LMB
 
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1LRP
 
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1MSC
 
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1RL0
 
 | Crystal structure of a new ribosome-inactivating protein (RIP): dianthin 30 | 分子名称: | Antiviral protein DAP-30 | 著者 | Fermani, S, Falini, G, Ripamonti, A, Bolognesi, A, Polito, L, Stirpe, F. | 登録日 | 2003-11-24 | 公開日 | 2004-12-07 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | The 1.4A structure of dianthin 30 indicates a role of surface potential at the active site of type 1 ribosome inactivating proteins J.Struct.Biol., 149, 2005
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1QIO
 
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1PMK
 
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1POZ
 
 | SOLUTION STRUCTURE OF THE HYALURONAN BINDING DOMAIN OF HUMAN CD44 | 分子名称: | CD44 antigen | 著者 | Teriete, P, Banerji, S, Blundell, C.D, Kahmann, J.D, Pickford, A.R, Wright, A.J, Campbell, I.D, Jackson, D.G, Day, A.J. | 登録日 | 2003-06-16 | 公開日 | 2004-03-16 | 最終更新日 | 2024-10-30 | 実験手法 | SOLUTION NMR | 主引用文献 | Structure of the Regulatory Hyaluronan Binding Domain in the Inflammatory Leukocyte Homing Receptor CD44. Mol.Cell, 13, 2004
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1PK2
 
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1PML
 
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1PBK
 
 | HOMOLOGOUS DOMAIN OF HUMAN FKBP25 | 分子名称: | FKBP25, RAPAMYCIN IMMUNOSUPPRESSANT DRUG | 著者 | Liang, J, Hung, D.T, Schreiber, S.L, Clardy, J. | 登録日 | 1995-09-01 | 公開日 | 1996-10-14 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structure of the human 25 kDa FK506 binding protein complexed with rapamycin. J.Am.Chem.Soc., 118, 1996
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