8CJN
Crystal structure of human tryptophan hydroxylase 1 in complex with inhibitor KM-06-070
Summary for 8CJN
Entry DOI | 10.2210/pdb8cjn/pdb |
Descriptor | Tryptophan 5-hydroxylase 1, FE (III) ION, 3-ethyl-7-[(4-phenylphenyl)methyl]-8-(5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-2-ylmethyl)purine-2,6-dione, ... (4 entities in total) |
Functional Keywords | catalytic domain of human tryptophan hydroxylase 1 (tph1), inhibitor complex, metal binding protein |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 37961.01 |
Authors | Schuetz, A.,Mallow, K.,Nazare, M.,Specker, E.,Heinemann, U. (deposition date: 2023-02-13, release date: 2024-01-10) |
Primary citation | Specker, E.,Wesolowski, R.,Schutz, A.,Matthes, S.,Mallow, K.,Wasinska-Kalwa, M.,Winkler, L.,Oder, A.,Alenina, N.,Pleimes, D.,von Kries, J.P.,Heinemann, U.,Bader, M.,Nazare, M. Structure-Based Design of Xanthine-Imidazopyridines and -Imidazothiazoles as Highly Potent and In Vivo Efficacious Tryptophan Hydroxylase Inhibitors. J.Med.Chem., 66:14866-14896, 2023 Cited by PubMed: 37905925DOI: 10.1021/acs.jmedchem.3c01454 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.6808093833 Å) |
Structure validation
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