Structure of PDB 4lfy Chain B Binding Site BS01
Receptor Information
>4lfy Chain B (length=353) Species:
216591
(Burkholderia cenocepacia J2315) [
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PMTASNASSPATLSLARPDDWHLHLRDGDMLAAVLPHTARQFGRAIVMPN
LKPPVTTTAQAQAYRERILAALPAGMTFEPLMTLYLTDNTPPDEIRRARE
SGFVHGVKLYPAGTNSDHGVTDLAKCAKTLEAMQETGMPLLVHGEVTDAS
IDLFDREKVFIDRVMTPLRRDFPGLKVVFEHITTKDAADYVRDADAAPGL
LGATITAHHLLYNRNALFVGGIRPHYYCLPVLKRETHRVALVEAATSGNP
RFFLGTDSAPHARDAKETACGCAGCYTALHALELYAEAFDTAGALDKLEG
FASFFGADFYGLPRSAETVTLRREPWELPREIFAGETPVVPLRGGETIGW
KLA
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
4lfy Chain A Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
4lfy
Crystal structure of a dihydroorotase from Burkholderia cenocepacia J2315
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
R225 R245
Binding residue
(residue number reindexed from 1)
R214 R234
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H31 H33 K117 H154 H192 D268
Catalytic site (residue number reindexed from 1)
H22 H24 K108 H143 H181 D257
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:0046872
metal ion binding
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0009220
pyrimidine ribonucleotide biosynthetic process
GO:0019856
pyrimidine nucleobase biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4lfy
,
PDBe:4lfy
,
PDBj:4lfy
PDBsum
4lfy
PubMed
UniProt
B4EEU0
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