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PDB files of models after energy minimisation
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创建时间：
2023-09-13
相关数据集
Supplementary Table S5 from Discovery and Characterization of VPRBP/DCAF1 Kinase Inhibitor Analogs as Microtubular Destabilizing Agents with Potent Antimyeloma Activity
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A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE
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Design and Optimization of Novel Benzimidazole- and Imidazo[4,5‑ b ]pyridine-Based ATM Kinase Inhibitors with Subnanomolar Activities
The ATM kinase is a promising target in cancer treatment as an important regulator of the cellular response to DNA double-strand breaks. In this work, we present a new class of specific benzimidazole-
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Crystal structure of HCV NS3/4A protease in complex with NR01-145
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Crystal structure of human JMJD2A in complex with compound 30
Crystal structure of human JMJD2A in complex with compound 30 Descriptor: 1,2-ETHANEDIOL, 2-(5-azanyl-2-oxidanyl-phenyl)pyridine-4-carboxylic acid, CHLORIDE ION, ... Authors: Velupillai, S, Krojer, T,
Protein Data Bank Japan2024-01-10 更新60
