Structure of PDB 2bx7 Chain B Binding Site BS03
Receptor Information
>2bx7 Chain B (length=311) Species:
1358
(Lactococcus lactis) [
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MLNTTFANAKFANPFMNASGVHCMTIEDLEELKASQAGAYITKSSTLEKR
EGNPLPRYVDLELGSINSMGLPNLGFDYYLDYVLKNQKENAQEGPIFFSI
AGMSAAENIAMLKKIQESDFSGITELNLSCPNVPGKPQLAYDFEATEKLL
KEVFTFFTKPLGVKLPPYFDLVHFDIMAEILNQFPLTYVNSVNSIGNGLF
IDPEAESVVIKPKDGFGGIGGAYIKPTALANVRAFYTRLKPEIQIIGTGG
IETGQDAFEHLLCGATMLQIGTALHKEGPAIFDRIIKELEEIMNQKGYQS
IADFHGKLKSL
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
2bx7 Chain B Residue 1314 [
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Receptor-Ligand Complex Structure
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PDB
2bx7
Interaction of Benzoate Pyrimidine Analogues with Class 1A Dihydroorotate Dehydrogenase from Lactococcus Lactis.
Resolution
2.04 Å
Binding residue
(original residue number in PDB)
K33 S35
Binding residue
(residue number reindexed from 1)
K33 S35
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K43 N67 L71 C130 N132 V133 K164 V192
Catalytic site (residue number reindexed from 1)
K43 N67 L71 C130 N132 V133 K164 V192
Enzyme Commision number
1.3.98.1
: dihydroorotate oxidase (fumarate).
Gene Ontology
Molecular Function
GO:0004152
dihydroorotate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:1990663
dihydroorotate dehydrogenase (fumarate) activity
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0006222
UMP biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2bx7
,
PDBe:2bx7
,
PDBj:2bx7
PDBsum
2bx7
PubMed
17444658
UniProt
A2RJT9
|PYRDA_LACLM Dihydroorotate dehydrogenase A (fumarate) (Gene Name=pyrDA)
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