Structure of PDB 2we0 Chain A Binding Site BS01
Receptor Information
>2we0 Chain A (length=247) Species:
10377
(Human herpesvirus 4 strain B95-8) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
PHIRYAFQNDKLLLQQASVGRLTLVNKTTILLRPMKTTTVDLGLYARPPE
GHGLMLWGSTSRPVTSHVGIIDPGYTGELRLILQNQRRYNSTLRPSELKI
HLAAFRYATPQGPINHPQYPGDVGLDVSLPKDLALFPHQTVSVTLTVPPP
SIPHHRPTIFGRSGLAMQGILVKPCRWRRGGVDVSLTNFSDQTVFLNKYR
RFCQLVYLHKHHLTSFYSPHSDAGVLGPRSLFRWASCTFEEVPSLAM
Ligand information
Ligand ID
UMP
InChI
InChI=1S/C9H13N2O8P/c12-5-3-8(11-2-1-7(13)10-9(11)14)19-6(5)4-18-20(15,16)17/h1-2,5-6,8,12H,3-4H2,(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1
InChIKey
JSRLJPSBLDHEIO-SHYZEUOFSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=P(O)(O)OCC2OC(N1C(=O)NC(=O)C=C1)CC2O
CACTVS 3.370
O[CH]1C[CH](O[CH]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.7.6
C1[C@@H]([C@H](O[C@H]1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
CACTVS 3.370
O[C@H]1C[C@@H](O[C@@H]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.7.6
C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
Formula
C9 H13 N2 O8 P
Name
2'-DEOXYURIDINE 5'-MONOPHOSPHATE;
DUMP
ChEMBL
CHEMBL211312
DrugBank
DB03800
ZINC
ZINC000004228260
PDB chain
2we0 Chain A Residue 1257 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
2we0
The Flexible Motif V of Epstein-Barr Virus Deoxyuridine 5'-Triphosphate Pyrophosphatase is Essential for Catalysis.
Resolution
2.01 Å
Binding residue
(original residue number in PDB)
G73 I75 D76 Y79 R84 R171 S172
Binding residue
(residue number reindexed from 1)
G69 I71 D72 Y75 R80 R162 S163
Annotation score
3
Binding affinity
MOAD
: Kd=37uM
Enzymatic activity
Enzyme Commision number
3.6.1.23
: dUTP diphosphatase.
Gene Ontology
Molecular Function
GO:0004170
dUTP diphosphatase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0009117
nucleotide metabolic process
GO:0046080
dUTP metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2we0
,
PDBe:2we0
,
PDBj:2we0
PDBsum
2we0
PubMed
19586911
UniProt
P03195
|DUT_EBVB9 Deoxyuridine 5'-triphosphate nucleotidohydrolase (Gene Name=DUT)
[
Back to BioLiP
]