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BU of 1vyz by Molmil

Structure of CDK2 complexed with PNU-181227
分子名称:	CELL DIVISION PROTEIN KINASE 2, N-(5-CYCLOPROPYL-1H-PYRAZOL-3-YL)BENZAMIDE
著者	Pevarello, P, Brasca, M.G, Amici, R, Orsini, P, Traquandi, G, Corti, L, Piutti, C, Sansonna, P, Villa, M, Pierce, B.S, Pulici, M, Giordano, G, Martina, K, Lfritzen, E, Nugent, R.A, Casale, E, Cameron, A, Ciomei, M, Roletto, F, Isacchi, A, Fogliatto, G, Pesenti, E, Pastori, W, Marsiglio, W, Leach, K.L, Clare, P.M, Fiorentini, F, Varasi, M, Vulpetti, A, Warpehoski, M.A.
登録日	2004-05-07
公開日	2004-06-17
最終更新日	2019-04-03
実験手法	X-RAY DIFFRACTION (2.21 Å)
主引用文献	3-Aminopyrazole Inhibitors of Cdk2/Cyclin a as Antitumor Agents. 1. Lead Finding J.Med.Chem., 47, 2004

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BU of 1vyw by Molmil

Structure of CDK2/Cyclin A with PNU-292137
分子名称:	CELL DIVISION PROTEIN KINASE 2, CYCLIN A2, N-(3-CYCLOPROPYL-1H-PYRAZOL-5-YL)-2-(2-NAPHTHYL)ACETAMIDE, ...
著者	Pevarello, P, Brasca, M.G, Amici, R, Orsini, P, Traquandi, G, Corti, L, Piutti, C, Sansonna, P, Villa, M, Pierce, B.S, Pulici, M, Giordano, P, Martina, K, Fritzen, E.L, Nugent, R.A, Casale, E, Cameron, A, Ciomei, M, Roletto, F, Isacchi, A, Fogliatto, G, Pesenti, E, Pastori, W, Marsiglio, A, Leach, K.L, Clare, P.M, Fiorentini, F, Varasi, M, Vulpetti, A, Warpehoski, M.A.
登録日	2004-05-07
公開日	2004-06-10
最終更新日	2019-04-03
実験手法	X-RAY DIFFRACTION (2.3 Å)
主引用文献	3-Aminopyrazole Inhibitors of Cdk2/Cyclin a as Antitumor Agents. Part 1. Lead Finding J.Med.Chem., 47, 2004

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BU of 3u1y by Molmil

Potent Inhibitors of LpxC for the Treatment of Gram-Negative Infections
分子名称:	(2R)-N-hydroxy-2-methyl-2-(methylsulfonyl)-4-{4'-[3-(morpholin-4-yl)propoxy]biphenyl-4-yl}butanamide, UDP-3-O-[3-hydroxymyristoyl] N-acetylglucosamine deacetylase, ZINC ION
著者	Brown, M, Abramite, J, Liu, S.
登録日	2011-09-30
公開日	2012-01-04
最終更新日	2023-09-13
実験手法	X-RAY DIFFRACTION (2 Å)
主引用文献	Potent inhibitors of LpxC for the treatment of Gram-negative infections. J.Med.Chem., 55, 2012

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BU of 3uhm by Molmil

UDP-3-O-[3-hydroxymyristoyl] N-acetylglucosamine deacetylase in complex with inhibitor
分子名称:	(2R)-N-hydroxy-2-methyl-2-(methylsulfonyl)-4-(2-oxo-4-phenylpyridin-1(2H)-yl)butanamide, 1,2-ETHANEDIOL, GUANIDINE, ...
著者	Montgomery, J, Liu, S.
登録日	2011-11-03
公開日	2012-02-01
最終更新日	2023-09-13
実験手法	X-RAY DIFFRACTION (1.26 Å)
主引用文献	Pyridone methylsulfone hydroxamate LpxC inhibitors for the treatment of serious gram-negative infections. J.Med.Chem., 55, 2012

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BU of 1jsv by Molmil

The structure of cyclin-dependent kinase 2 (CDK2) in complex with 4-[(6-amino-4-pyrimidinyl)amino]benzenesulfonamide
分子名称:	4-[(6-AMINO-4-PYRIMIDINYL)AMINO]BENZENESULFONAMIDE, CELL DIVISION PROTEIN KINASE 2
著者	Watenpaugh, K.D, Kelley, L.C.
登録日	2001-08-19
公開日	2001-08-29
最終更新日	2024-02-07
実験手法	X-RAY DIFFRACTION (1.96 Å)
主引用文献	The cyclin-dependent kinases cdk2 and cdk5 act by a random, anticooperative kinetic mechanism J.Biol.Chem., 276, 2001

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