7ZIF
Crystal structure of human tryptophan hydroxylase 1 in complex with inhibitor KM-480
Summary for 7ZIF
Entry DOI | 10.2210/pdb7zif/pdb |
Descriptor | Tryptophan 5-hydroxylase 1, FE (III) ION, (2R)-2-azanyl-5-[[2-[3-methyl-2,6-bis(oxidanylidene)-7-(phenylmethyl)purin-8-yl]sulfanyl-3H-benzimidazol-5-yl]amino]-5-oxidanylidene-pentanoic acid, ... (5 entities in total) |
Functional Keywords | tryptophan hydroxylase, serotonin biosynthesis, metal binding protein |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 38121.11 |
Authors | Schuetz, A.,Ziebart, N.,Weise, M.,Mallow, K.,Pfeifer, J.,Nazare, M.,Specker, E.,Heinemann, U. (deposition date: 2022-04-08, release date: 2022-09-07, Last modification date: 2024-01-31) |
Primary citation | Specker, E.,Matthes, S.,Wesolowski, R.,Schutz, A.,Grohmann, M.,Alenina, N.,Pleimes, D.,Mallow, K.,Neuenschwander, M.,Gogolin, A.,Weise, M.,Pfeifer, J.,Ziebart, N.,Heinemann, U.,von Kries, J.P.,Nazare, M.,Bader, M. Structure-Based Design of Xanthine-Benzimidazole Derivatives as Novel and Potent Tryptophan Hydroxylase Inhibitors. J.Med.Chem., 65:11126-11149, 2022 Cited by PubMed: 35921615DOI: 10.1021/acs.jmedchem.2c00598 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.86859719255 Å) |
Structure validation
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