Structure of PDB 3eww Chain B Binding Site BS01
Receptor Information
>3eww Chain B (length=257) Species:
9606
(Homo sapiens) [
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MELSFGARAELPRIHPVASKLLRLMQKKETNLCLSADVSLARELLQLADA
LGPSICMLKTHVDILNDFTLDVMKELITLAKCHEFLIFENRKFADIGNTV
KKQYEGGIFKIASWADLVNAHVVPGSGVVKGLQEVGLPLHRGCLLIAEMS
STGSLATGDYTRAAVRMAEEHSEFVVGFISGSRVSMKPEFLHLTPGVQLE
AGGDNLGQQYNSPQEVIGKRGSDIIIVGRGIISAADRLEAAEMYRKAAWE
AYLSRLG
Ligand information
Ligand ID
U1P
InChI
InChI=1S/C10H14N3O9P/c11-2-4-1-6(14)12-10(17)13(4)9-8(16)7(15)5(22-9)3-21-23(18,19)20/h1-2,5,7-9,11,15-16H,3H2,(H,12,14,17)(H2,18,19,20)/b11-2+/t5-,7-,8-,9-/m1/s1
InChIKey
GSNYQYNODBCZBM-XDMCGQROSA-N
SMILES
Software
SMILES
CACTVS 3.341
O[CH]1[CH](O)[CH](O[CH]1CO[P](O)(O)=O)N2C(=O)NC(=O)C=C2C=N
ACDLabs 10.04
O=C1NC(=O)N(C(C=[N@H])=C1)C2OC(C(O)C2O)COP(=O)(O)O
OpenEye OEToolkits 1.5.0
[H]N=CC1=CC(=O)NC(=O)N1C2C(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(=O)NC(=O)C=C2C=N
OpenEye OEToolkits 1.5.0
[H]/N=C/C1=CC(=O)NC(=O)N1[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
Formula
C10 H14 N3 O9 P
Name
6-[(E)-iminomethyl]uridine 5'-phosphate
ChEMBL
DrugBank
ZINC
PDB chain
3eww Chain A Residue 482 [
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Receptor-Ligand Complex Structure
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PDB
3eww
Lys314 is a nucleophile in non-classical reactions of orotidine-5'-monophosphate decarboxylase
Resolution
1.1 Å
Binding residue
(original residue number in PDB)
D317 I318 T321
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:3eww
,
PDBe:3eww
,
PDBj:3eww
PDBsum
3eww
PubMed
19472232
UniProt
P11172
|UMPS_HUMAN Uridine 5'-monophosphate synthase (Gene Name=UMPS)
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