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8ZUD

Crystal Structure of Human Myt1 Kinase domain Bounded with compound 8f

This is a non-PDB format compatible entry.
Summary for 8ZUD
Entry DOI10.2210/pdb8zud/pdb
DescriptorMembrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase, 2-azanyl-3-(2,6-dimethyl-3-oxidanyl-phenyl)-5-(2-morpholin-4-ylpyridin-4-yl)benzamide (3 entities in total)
Functional Keywordsprotein kinase, gene regulation
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight32129.57
Authors
Zhang, Z.M.,Zhou, Z.Q. (deposition date: 2024-06-08, release date: 2024-09-11, Last modification date: 2024-09-25)
Primary citationWang, C.,Fang, Y.,Zhou, Z.,Liu, Z.,Feng, F.,Wan, X.,Li, Y.,Liu, S.,Ding, J.,Zhang, Z.M.,Xie, H.,Lu, X.
Structure-Based Drug Design of 2-Amino-[1,1'-biphenyl]-3-carboxamide Derivatives as Selective PKMYT1 Inhibitors for the Treatment of CCNE1 -Amplified Breast Cancer.
J.Med.Chem., 67:15816-15836, 2024
Cited by
PubMed: 39163619
DOI: 10.1021/acs.jmedchem.4c01458
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5051008788 Å)
Structure validation

225946

数据于2024-10-09公开中

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