Structure of PDB 4xiy Chain D Binding Site BS02
Receptor Information
>4xiy Chain D (length=328) Species:
322710
(Azotobacter vinelandii DJ) [
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MKVYYDKDCDLSIIQSKKVAIIGYGSQGHAHACNLKDSGVDVYVGLRAGS
ASVAKAEAHGLTVKSVKDAVAAADVVMILTPDEFQGRLYKDEIEPNLKKG
ATLAFAHGFSIHYNQVVPRADLDVIMIAPKAPGHTVRSEFVRGGGIPDLI
AVYQDASGNAKNLALSYACGVGGGRTGIIETTFKDETETDLFGEQAVLCG
GCVELVKAGFETLVEAGYAPEMAYFECLHELKLIVDLMFEGGIANMNYSI
SNNAEYGEYVTGPEVINEQSRQAMRNALKRIQDGEYAKMFITEGAANYPS
MTAYRRNNAAHQIEVVGEKLRTMMPWIA
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
4xiy Chain D Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4xiy
Cofactor specificity motifs and the induced fit mechanism in class I ketol-acid reductoisomerases.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D190 E194
Binding residue
(residue number reindexed from 1)
D190 E194
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K130 D190 E194
Catalytic site (residue number reindexed from 1)
K130 D190 E194
Enzyme Commision number
1.1.1.86
: ketol-acid reductoisomerase (NADP(+)).
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004455
ketol-acid reductoisomerase activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050661
NADP binding
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009082
branched-chain amino acid biosynthetic process
GO:0009097
isoleucine biosynthetic process
GO:0009099
L-valine biosynthetic process
Cellular Component
GO:0005829
cytosol
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Cellular Component
External links
PDB
RCSB:4xiy
,
PDBe:4xiy
,
PDBj:4xiy
PDBsum
4xiy
PubMed
25849365
UniProt
C1DFH7
|ILVC_AZOVD Ketol-acid reductoisomerase (NADP(+)) (Gene Name=ilvC)
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