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5V1B

Structure of PHD1 in complex with 1,2,4-Triazolo-[1,5-a]pyridine

Summary for 5V1B
Entry DOI10.2210/pdb5v1b/pdb
Related5V18
DescriptorEgl nine homolog 2, SULFATE ION, FE (III) ION, ... (5 entities in total)
Functional Keywordshif prolylhydroxylase domain-1, inhibitor, momodentate binding, oxidoreductase-inhibitor complex, oxidoreductase/inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationNucleus : Q96KS0
Total number of polymer chains1
Total formula weight27033.64
Authors
Skene, R.J. (deposition date: 2017-03-01, release date: 2017-06-21, Last modification date: 2024-03-06)
Primary citationAhmed, S.,Ayscough, A.,Barker, G.R.,Canning, H.E.,Davenport, R.,Downham, R.,Harrison, D.,Jenkins, K.,Kinsella, N.,Livermore, D.G.,Wright, S.,Ivetac, A.D.,Skene, R.,Wilkens, S.J.,Webster, N.A.,Hendrick, A.G.
1,2,4-Triazolo-[1,5-a]pyridine HIF Prolylhydroxylase Domain-1 (PHD-1) Inhibitors With a Novel Monodentate Binding Interaction.
J. Med. Chem., 60:5663-5672, 2017
Cited by
PubMed: 28594552
DOI: 10.1021/acs.jmedchem.7b00352
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.49 Å)
Structure validation

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