Structure of PDB 1xge Chain A Binding Site BS01
Receptor Information
>1xge Chain A (length=343) Species:
562
(Escherichia coli) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
SQVLKIRRPDDWHLHLRDGDMLKTVVPYTSEIYGRAIVMPNLAPPVTTVE
AAVAYRQRILDAVPAGHDFTPLMTCYLTDSLDPNELERGFNEGVFTAAKL
YPANATTNSSHGVTSVDAIMPVLERMEKIGMPLLVHGEVTHADIDIFDRE
ARFIESVMEPLRQRLTALKVVFEHITTKDAADYVRDGNERLAATITPQHL
MFNRNHMLVGGVRPHLYCLPILKRNIHQQALRELVASGFNRVFLGTDSAP
HARHRKESSCGCAGCFNAPTALGSYATVFEEMNALQHFEAFCSVNGPQFY
GLPVNDTFIELVREEQQVAESIALTDDTLVPFLAGETVRWSVK
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
1xge Chain A Residue 400 [
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
1xge
Dihydroorotase from Escherichia coli: Loop Movement and Cooperativity between Subunits
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
K102 H139 H177
Binding residue
(residue number reindexed from 1)
K99 H136 H174
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H16 H18 K102 H139 H177 D250
Catalytic site (residue number reindexed from 1)
H13 H15 K99 H136 H174 D247
Enzyme Commision number
3.5.2.3
: dihydroorotase.
Gene Ontology
Molecular Function
GO:0004151
dihydroorotase activity
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0016812
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0019856
pyrimidine nucleobase biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1xge
,
PDBe:1xge
,
PDBj:1xge
PDBsum
1xge
PubMed
15826651
UniProt
P05020
|PYRC_ECOLI Dihydroorotase (Gene Name=pyrC)
[
Back to BioLiP
]