4D6Z
Cytochrome P450 3A4 bound to imidazole and an inhibitor
Summary for 4D6Z
Entry DOI | 10.2210/pdb4d6z/pdb |
Related | 4D75 |
Descriptor | CYTOCHROME P450 3A4, PROTOPORPHYRIN IX CONTAINING FE, tert-butyl {6-oxo-6-[(pyridin-3-ylmethyl)amino]hexyl}carbamate, ... (6 entities in total) |
Functional Keywords | oxidoreductase, monooxygenase, cytochrome p450, human cyp3a4, imidazole, inhibitory complex |
Biological source | HOMO SAPIENS (HUMAN) |
Cellular location | Endoplasmic reticulum membrane; Single-pass membrane protein: P08684 |
Total number of polymer chains | 1 |
Total formula weight | 57017.04 |
Authors | Sevrioukova, I.,Poulos, T. (deposition date: 2014-11-19, release date: 2015-09-23, Last modification date: 2023-12-20) |
Primary citation | Kaur, P.,Chamberlin, R.,Poulos, T.L.,Sevrioukova, I.F. Structure-Based Inhibitor Design for Evaluation of a Cyp3A4 Pharmacophore Model. J.Med.Chem., 59:4210-, 2016 Cited by PubMed: 26371436DOI: 10.1021/ACS.JMEDCHEM.5B01146 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.93 Å) |
Structure validation
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