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2FDW

Crystal Structure Of Human Microsomal P450 2A6 with the inhibitor (5-(Pyridin-3-yl)furan-2-yl)methanamine bound

Summary for 2FDW
Entry DOI10.2210/pdb2fdw/pdb
Related1Z10 1Z11 2FDU 2FDV 2FDY
DescriptorCytochrome P450 2A6, PROTOPORPHYRIN IX CONTAINING FE, (5-(PYRIDIN-3-YL)FURAN-2-YL)METHANAMINE, ... (4 entities in total)
Functional Keywordscyp2a6, p450 2a6, p450, monooxygenase, drug metabolizing enzyme, coumarin 7-hydroxylase, nicotine oxidase, oxidoreductase
Biological sourceHomo sapiens (human)
Cellular locationEndoplasmic reticulum membrane; Peripheral membrane protein: P11509
Total number of polymer chains4
Total formula weight221849.29
Authors
Yano, J.K.,Stout, C.D.,Johnson, E.F. (deposition date: 2005-12-14, release date: 2006-11-28, Last modification date: 2023-08-30)
Primary citationYano, J.K.,Denton, T.T.,Cerny, M.A.,Zhang, X.,Johnson, E.F.,Cashman, J.R.
Synthetic Inhibitors of Cytochrome P-450 2A6: Inhibitory Activity, Difference Spectra, Mechanism of Inhibition, and Protein Cocrystallization.
J.Med.Chem., 49:6987-7001, 2006
Cited by
PubMed: 17125252
DOI: 10.1021/jm060519r
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

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