Structure of PDB 3dbp Chain A Binding Site BS02
Receptor Information
>3dbp Chain A (length=257) Species:
9606
(Homo sapiens) [
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KELSFGARAELPRIHPVASKLLRLMQKKETNLCLSADVSLARELLQLADA
LGPSICMLKTHVDILNDFTLDVMKELITLAKCHEFLIFEDRKFADIGNTV
KKQYEGGIFKIASWADLVNAHVVPGSGVVKGLQEVGLPLHRGCLLIAEMS
STGSLATGDYTRAAVRMAEEHSEFVVGFISGSRVSMKPEFLHLTPGVQLE
AGGDNLGQQYNSPQEVIGKRGSDIIIVGRGIISAADRLEAAEMYRKAAWE
AYLSRLG
Ligand information
Ligand ID
NUP
InChI
InChI=1S/C9H14N3O9P/c10-4-1-5(13)11-9(16)12(4)8-7(15)6(14)3(21-8)2-20-22(17,18)19/h1,3,6-8,14-15H,2,10H2,(H,11,13,16)(H2,17,18,19)/t3-,6-,7-,8-/m1/s1
InChIKey
DUFXRFNPGXQQOI-YXZULKJRSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=C(N(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O)N
CACTVS 3.341
NC1=CC(=O)NC(=O)N1[C@@H]2O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]2O
ACDLabs 10.04
O=C1NC(=O)N(C(N)=C1)C2OC(C(O)C2O)COP(=O)(O)O
OpenEye OEToolkits 1.5.0
C1=C(N(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O)N
CACTVS 3.341
NC1=CC(=O)NC(=O)N1[CH]2O[CH](CO[P](O)(O)=O)[CH](O)[CH]2O
Formula
C9 H14 N3 O9 P
Name
6-AMINOURIDINE 5'-MONOPHOSPHATE
ChEMBL
CHEMBL514137
DrugBank
ZINC
ZINC000014975890
PDB chain
3dbp Chain B Residue 1000 [
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Receptor-Ligand Complex Structure
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PDB
3dbp
Crystal Structure of Human Orotidine 5'-Monophosphate Decarboxylase Complexed with 6-NH2-UMP
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
D128 I129 T132
Binding residue
(residue number reindexed from 1)
D95 I96 T99
Annotation score
2
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
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Biological Process
External links
PDB
RCSB:3dbp
,
PDBe:3dbp
,
PDBj:3dbp
PDBsum
3dbp
PubMed
UniProt
P11172
|UMPS_HUMAN Uridine 5'-monophosphate synthase (Gene Name=UMPS)
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