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7ZIK

Crystal structure of human tryptophan hydroxylase 1 in complex with inhibitor LP533401

Summary for 7ZIK
Entry DOI10.2210/pdb7zik/pdb
DescriptorTryptophan 5-hydroxylase 1, FE (III) ION, (2~{R})-2-azanyl-3-[4-[2-azanyl-6-[(1~{R})-1-[4-chloranyl-2-(3-methylpyrazol-1-yl)phenyl]-2,2,2-tris(fluoranyl)ethoxy]pyrimidin-4-yl]phenyl]propanoic acid, ... (4 entities in total)
Functional Keywordstryptophan hydroxylase, serotonin biosynthesis, metal binding protein
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight76054.75
Authors
Schuetz, A.,Heinemann, U. (deposition date: 2022-04-08, release date: 2022-09-07, Last modification date: 2024-01-31)
Primary citationSpecker, 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: 35921615
DOI: 10.1021/acs.jmedchem.2c00598
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.58925907124 Å)
Structure validation

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