Structure of PDB 5lbf Chain A Binding Site BS02
Receptor Information
>5lbf Chain A (length=224) Species:
9606
(Homo sapiens) [
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LPALKLALEYIVPCMNKHGICVVDDFLGKETGQQIGDEVRALHDTGKFTD
GQLVSQKSDSSKDIRGDKITWIEGKEPGCETIGLLMSSMDDLIRHCNGKL
GSYKIKERTKAMVACYPGNGTGYVRHVDNPNGDGRCVTCIYYLNKDWDAK
VSGGILRIFPEGKAQFADIEPKFDRLLFFWSDRRNPHEVQPAYATRYAIT
VWYFDADERARAKVKYLEKGVRVE
Ligand information
Ligand ID
UN9
InChI
InChI=1S/C12H9ClN2O4/c13-11-7-4-2-1-3-6(7)10(18)9(15-11)12(19)14-5-8(16)17/h1-4,18H,5H2,(H,14,19)(H,16,17)
InChIKey
OUQVKRKGTAUJQA-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OC(=O)CNC(=O)c1nc(Cl)c2ccccc2c1O
OpenEye OEToolkits 1.5.0
c1ccc2c(c1)c(c(nc2Cl)C(=O)NCC(=O)O)O
ACDLabs 10.04
O=C(O)CNC(=O)c1nc(Cl)c2c(c1O)cccc2
Formula
C12 H9 Cl N2 O4
Name
N-[(1-CHLORO-4-HYDROXYISOQUINOLIN-3-YL)CARBONYL]GLYCINE
ChEMBL
CHEMBL426560
DrugBank
DB08687
ZINC
ZINC000000007670
PDB chain
5lbf Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
5lbf
Structural basis for oxygen degradation domain selectivity of the HIF prolyl hydroxylases.
Resolution
1.8995 Å
Binding residue
(original residue number in PDB)
D254 M299 Y303 Y310 H313 Y329 L343 H374 V376 R383
Binding residue
(residue number reindexed from 1)
D67 M112 Y116 Y123 H126 Y142 L156 H187 V189 R196
Annotation score
1
Binding affinity
BindingDB: IC50=300nM,EC50=79000nM,Kd=80nM
Enzymatic activity
Enzyme Commision number
1.14.11.29
: hypoxia-inducible factor-proline dioxygenase.
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0031418
L-ascorbic acid binding
View graph for
Molecular Function
External links
PDB
RCSB:5lbf
,
PDBe:5lbf
,
PDBj:5lbf
PDBsum
5lbf
PubMed
27561929
UniProt
Q9GZT9
|EGLN1_HUMAN Egl nine homolog 1 (Gene Name=EGLN1)
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