Structure of PDB 5eks Chain B Binding Site BS02
Receptor Information
>5eks Chain B (length=354) Species:
470
(Acinetobacter baumannii) [
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HHMQTLHVELRRYPIFIGSQLDPKQLLEPYIHGQQVMIVSNVTVAPLYLS
HYQEALESLGKTVATCILPDGEKYKDIQHLNLIFDALLEAGFNRDCTVLA
LGGGVIGDMAGFASACFQRGVYFVQVPTTLLSQVDSSVGGKTGINHPLGK
NMLGAFQQPQVVLADMAQLNTLPERELSAGLAEVIKYALLGDEDFLVWLE
ENMDGLVARDADLLAEAVYRSCAHKARIVANDEERALLNLGHTFGHAIES
YLGYGTWLHGEAVATGMVMAADLSQRLGWISNEDVARTKKIIQRANLPIS
CPQIPLDDFLGYMAHDKKVGQLRLVLLKQLGQAVITKDFDVELMKQAILA
NQHG
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
5eks Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5eks
Structure of 3-dehydroquinate synthase from Acinetobacter baumannii in complex with NAD
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
E183 H246 H263
Binding residue
(residue number reindexed from 1)
E183 H242 H259
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R119 K141 E183 K225 R239 N243 H246 H250 H263
Catalytic site (residue number reindexed from 1)
R119 K141 E183 K225 R235 N239 H242 H246 H259
Enzyme Commision number
4.2.3.4
: 3-dehydroquinate synthase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003856
3-dehydroquinate synthase activity
GO:0016829
lyase activity
GO:0016838
carbon-oxygen lyase activity, acting on phosphates
GO:0046872
metal ion binding
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009073
aromatic amino acid family biosynthetic process
GO:0009423
chorismate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5eks
,
PDBe:5eks
,
PDBj:5eks
PDBsum
5eks
PubMed
UniProt
V5V8R5
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