9JTX: Factor inhibiting HIF-1 alpha

Factor inhibiting HIF-1 alpha in complex with Zn(II) and 2-(4-hydroxy-2-oxo-1-(thiazol-4-ylmethoxy)-1,2-dihydroquinoline-3-carboxamido)-2-methylpropanoic acid. Determined by X-ray diffraction at 2.08 Å resolution. Released 30 Apr 2025.

Method
X-ray diffraction
Resolution
2.08 Å
Organism
Homo sapiens
Chains
1
Atoms
2,920
Mol. weight
41.47 kDa
Ligands
A1L4V, ZN
Released
30 Apr 2025

Explore 9JTX in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

9JTX contains 24 α-helices and 20 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 24 helices, 20 β-strands

ElementResiduesLengthSheet
α-helix16-172
β-strand1811
α-helix191
α-helix20-223
β-strand2511
α-helix29-313
α-helix33-342
β-strand39-4132
α-helix42-432
β-strand44-4523
α-helix50-578
β-strand62-6433
α-helix71-755
α-helix78-847
β-strand90-9563
β-strand9912
α-helix105-1095
β-strand120-12343
α-helix125-13814
β-strand143-14973
α-helix156-1638
α-helix167-17610
β-strand182-19093
β-strand195-19952
β-strand204-21183
β-strand214-21962
α-helix221-2233
α-helix224-2274
β-strand22914
α-helix230-2312
β-strand23912
β-strand24014
α-helix253-2575
β-strand260-26562
β-strand270-27343
β-strand278-28362
α-helix2841
β-strand290-29783
α-helix298-3036
α-helix306-3072
α-helix310-3112
α-helix312-32918
α-helix333-3353
α-helix336-3449

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Hypoxia-inducible factor 1-alpha inhibitorAprotein349Homo sapiensQ9NWT6 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>9JTX_1 Hypoxia-inducible factor 1-alpha inhibitor (chains A)
MAATAAEAVASGSGEPREEAGALGPAWDESQLRSYSFPTRPIPRLSQSDPRAEELIENEE
PVVLTDTNLVYPALKWDLEYLQENIGNGDFSVYSASTHKFLYYDEKKMANFQNFKPRSNR
EEMKFHEFVEKLQDIQQRGGEERLYLQQTLNDTVGRKIVMDFLGFNWNWINKQQGKRGWG
QLTSNLLLIGMEGNVTPAHYDEQQNFFAQIKGYKRCILFPPDQFECLYPYPVHHPCDRQS
QVDFDNPDYERFPNFQNVVGYETVVGPGDVLYIPMYWWHHIESLLNGGITITVNFWYKGA
PTPKRIEYPLKAHQKVAIMRNIEKMLGEALGNPQEVGPLLNTMIKGRYN

Ligands and cofactors

IDNameFormulaCopies
A1L4V2-methyl-2-[[4-oxidanyl-2-oxidanylidene-1-(1,3-thiazol-4-ylmethoxy)quinolin-3-y…C18 H17 N3 O6 S1
ZNZinc ionZn1

Water and common crystallization additives (SO4) are not listed.

Primary citation

Derivatives of the Clinically Used HIF Prolyl Hydroxylase Inhibitor Desidustat Are Efficient Inhibitors of Human gamma-Butyrobetaine Hydroxylase. Corner, T.P., Tumber, A., Salah, E. et al. J Med Chem (2025) 68:9777-9798. DOI 10.1021/acs.jmedchem.5c00586 · PubMed

Other PDB entries of the same protein (UniProt Q9NWT6 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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