Structure of PDB 4hkp Chain B Binding Site BS02
Receptor Information
>4hkp Chain B (length=256) Species:
9606
(Homo sapiens) [
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ELSFGARAELPRIHPVASKLLRLMQKKETNLCLSADVSLARELLQLADAL
GPSICMLKTHVDILNDFTLDVMKELITLAKCHEFLIFEDRKFADIGNTVK
KQYEGGIFKIASWADLVNAHVVPGSGVVKGLQEVGLPLHRGCLLIAEMSS
TGSLATGDYTRAAVRMAEEHSEFVVGFISGSRVSMKPEFLHLTPGVQLEA
GGDNLGQQYNSPQEVIGKRGSDIIIVGRGIISAADRLEAAEMYRKAAWEA
YLSRLG
Ligand information
Ligand ID
16B
InChI
InChI=1S/C9H14N3O9P/c13-6-4(3-20-22(17,18)19)21-8(7(6)14)12-2-1-5(11-16)10-9(12)15/h1-2,4,6-8,13-14,16H,3H2,(H,10,11,15)(H2,17,18,19)/t4-,6-,7-,8-/m1/s1
InChIKey
DYOUVDKCXLKHKY-XVFCMESISA-N
SMILES
Software
SMILES
CACTVS 3.385
ONC1=NC(=O)N(C=C1)[CH]2O[CH](CO[P](O)(O)=O)[CH](O)[CH]2O
OpenEye OEToolkits 2.0.7
C1=CN(C(=O)N=C1NO)C2C(C(C(O2)COP(=O)(O)O)O)O
CACTVS 3.385
ONC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]2O
OpenEye OEToolkits 2.0.7
C1=CN(C(=O)N=C1NO)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
ACDLabs 12.01
O=P(O)(O)OCC1OC(N2C=CC(=NC2=O)NO)C(O)C1O
Formula
C9 H14 N3 O9 P
Name
N-hydroxycytidine 5'-(dihydrogen phosphate)
ChEMBL
CHEMBL2221214
DrugBank
ZINC
PDB chain
4hkp Chain A Residue 305 [
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Receptor-Ligand Complex Structure
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PDB
4hkp
Novel cytidine-based orotidine-5'-monophosphate decarboxylase inhibitors with an unusual twist.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
D128 I129 T132
Binding residue
(residue number reindexed from 1)
D94 I95 T98
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.4.2.10
: orotate phosphoribosyltransferase.
4.1.1.23
: orotidine-5'-phosphate decarboxylase.
Gene Ontology
Molecular Function
GO:0004590
orotidine-5'-phosphate decarboxylase activity
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4hkp
,
PDBe:4hkp
,
PDBj:4hkp
PDBsum
4hkp
PubMed
22991951
UniProt
P11172
|UMPS_HUMAN Uridine 5'-monophosphate synthase (Gene Name=UMPS)
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