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6O3I

Crystal Structure of Human IDO1 bound to navoximod (NLG-919)

Summary for 6O3I
Entry DOI10.2210/pdb6o3i/pdb
DescriptorIndoleamine 2,3-dioxygenase 1, PROTOPORPHYRIN IX CONTAINING FE, trans-4-{(1R)-2-[(5S)-6-fluoro-5H-imidazo[5,1-a]isoindol-5-yl]-1-hydroxyethyl}cyclohexan-1-ol, ... (4 entities in total)
Functional Keywordsdioxygenase, tryptophan, ido, tdo, oxidoreductase-inhibitor complex, oxidoreductase/inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight96686.32
Authors
Harris, S.F.,Oh, A. (deposition date: 2019-02-26, release date: 2019-07-17, Last modification date: 2019-08-07)
Primary citationKumar, S.,Waldo, J.P.,Jaipuri, F.A.,Marcinowicz, A.,Van Allen, C.,Adams, J.,Kesharwani, T.,Zhang, X.,Metz, R.,Oh, A.J.,Harris, S.F.,Mautino, M.R.
Discovery of Clinical Candidate (1R,4r)-4-((R)-2-((S)-6-Fluoro-5H-imidazo[5,1-a]isoindol-5-yl)-1-hydroxyethyl)cyclohexan-1-ol (Navoximod), a Potent and Selective Inhibitor of Indoleamine 2,3-Dioxygenase 1.
J.Med.Chem., 62:6705-6733, 2019
Cited by
PubMed: 31264862
DOI: 10.1021/acs.jmedchem.9b00662
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.69 Å)
Structure validation

218500

數據於2024-04-17公開中

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