4ZSD
Human Cyclophilin D Complexed with an Inhibitor at room temperature
Summary for 4ZSD
Entry DOI | 10.2210/pdb4zsd/pdb |
Related | 4J5C |
Descriptor | Peptidyl-prolyl cis-trans isomerase F, mitochondrial, 1-(4-aminobenzyl)-3-[(2S)-4-(methylsulfanyl)-1-{(2R)-2-[2-(methylsulfanyl)phenyl]pyrrolidin-1-yl}-1-oxobutan-2-yl]urea (3 entities in total) |
Functional Keywords | isomerase inhibitor complex, isomerase |
Biological source | Homo sapiens (Human) |
Cellular location | Mitochondrion matrix : P30405 |
Total number of polymer chains | 1 |
Total formula weight | 18124.79 |
Authors | Gelin, M.,Delfosse, V.,Allemand, F.,Hoh, F.,Sallaz-Damaz, Y.,Pirocchi, M.,Bourguet, W.,Ferrer, J.-L.,Labesse, G.,Guichou, J.-F. (deposition date: 2015-05-13, release date: 2015-08-12, Last modification date: 2015-08-19) |
Primary citation | Gelin, M.,Delfosse, V.,Allemand, F.,Hoh, F.,Sallaz-Damaz, Y.,Pirocchi, M.,Bourguet, W.,Ferrer, J.L.,Labesse, G.,Guichou, J.F. Combining `dry' co-crystallization and in situ diffraction to facilitate ligand screening by X-ray crystallography. Acta Crystallogr.,Sect.D, 71:1777-1787, 2015 Cited by PubMed: 26249358DOI: 10.1107/S1399004715010342 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.45 Å) |
Structure validation
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