Structure of PDB 3ex6 Chain A Binding Site BS01
Receptor Information
>3ex6 Chain A (length=257) Species:
9606
(Homo sapiens) [
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MELSFGARAELPRIHPVASKLLRLMQKKETNLCLSADVSLARELLQLADA
LGPSICMLKTHVDILNDFTLDVMKELITLAKCHEFLIFENRKFADIGNTV
KKQYEGGIFKIASWADLVNAHVVPGSGVVKGLQEVGLPLHRGCLLIAEMS
STGSLATGDYTRAAVRMAEEHSEFVVGFISGSRVSMKPEFLHLTPGVQLE
AGGDNLGQQYNSPQEVIGKRGSDIIIVGRGIISAADRLEAAEMYRKAAWE
AYLSRLG
Ligand information
Ligand ID
U5P
InChI
InChI=1S/C9H13N2O9P/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChIKey
DJJCXFVJDGTHFX-XVFCMESISA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C1NC(=O)N(C=C1)C2OC(C(O)C2O)COP(=O)(O)O
CACTVS 3.341
O[CH]1[CH](O)[CH](O[CH]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O
CACTVS 3.341
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
Formula
C9 H13 N2 O9 P
Name
URIDINE-5'-MONOPHOSPHATE
ChEMBL
CHEMBL214393
DrugBank
DB03685
ZINC
ZINC000002123545
PDB chain
3ex6 Chain B Residue 482 [
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Receptor-Ligand Complex Structure
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PDB
3ex6
Lys314 is a nucleophile in non-classical reactions of orotidine-5'-monophosphate decarboxylase
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
D317 I318 T321
Binding residue
(residue number reindexed from 1)
D95 I96 T99
Annotation score
3
Binding affinity
PDBbind-CN
: -logKd/Ki=3.66,Ki=220uM
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:3ex6
,
PDBe:3ex6
,
PDBj:3ex6
PDBsum
3ex6
PubMed
19472232
UniProt
P11172
|UMPS_HUMAN Uridine 5'-monophosphate synthase (Gene Name=UMPS)
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