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3N7O

X-ray structure of human chymase in complex with small molecule inhibitor.

Summary for 3N7O
Entry DOI10.2210/pdb3n7o/pdb
DescriptorChymase, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, (S)-[(1S)-1-(5-chloro-1-benzothiophen-3-yl)-2-{[(E)-2-(3,4-difluorophenyl)ethenyl]amino}-2-oxoethyl]methylphosphinic acid, ... (5 entities in total)
Functional Keywordsserine protease, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight26300.47
Authors
Abad, M.C.,Kervinen, J.,Crysler, C.,Bayoumy, S.,Spurlino, J.,Deckman, I.,Greco, M.N.,Maryanoff, B.E.,Degaravilla, L. (deposition date: 2010-05-27, release date: 2010-07-21, Last modification date: 2023-09-06)
Primary citationKervinen, J.,Crysler, C.,Bayoumy, S.,Abad, M.C.,Spurlino, J.,Deckman, I.,Greco, M.N.,Maryanoff, B.E.,de Garavilla, L.
Potency variation of small-molecule chymase inhibitors across species.
Biochem. Pharmacol., 80:1033-1041, 2010
Cited by
PubMed: 20599788
DOI: 10.1016/j.bcp.2010.06.014
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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