Structure of PDB 4elx Chain A Binding Site BS01
Receptor Information
>4elx Chain A (length=268) Species:
83333
(Escherichia coli K-12) [
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PDEAMLYAPVEWHDCSEGFEDIRYEKSTDGIAKITINRPQVRNAFRPLTV
KEMIQALADARYDDNIGVIILTGAGDKAFCSGGDQKHHLNVLDFQRQIRT
CPKPVVAMVAGYSIGGGHVLHMMCDLTIAADNAIFGQTGPKVGSFDGGWG
ASYMARIVGQKKAREIWFLCRQYDAKQALDMGLVNTVVPLADLEKETVRW
CREMLQNSPMALRCLKAALNADCDGQAGLQELAGNATMLFYMTEEGQEGR
NAFNQKRQPDFSKFKRNP
Ligand information
Ligand ID
CL
InChI
InChI=1S/ClH/h1H/p-1
InChIKey
VEXZGXHMUGYJMC-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Cl-]
Formula
Cl
Name
CHLORIDE ION
ChEMBL
DrugBank
DB14547
ZINC
PDB chain
4elx Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
4elx
Active site binding and catalytic role of bicarbonate in 1,4-dihydroxy-2-naphthoyl coenzyme A synthases from vitamin K biosynthetic pathways
Resolution
2.191 Å
Binding residue
(original residue number in PDB)
G132 G156 W184
Binding residue
(residue number reindexed from 1)
G115 G139 W167
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G86 H105 L109 G133 V136 G156 S161 D163 G164 A250 Y258
Catalytic site (residue number reindexed from 1)
G83 H88 L92 G116 V119 G139 S144 D146 G147 A233 Y241
Enzyme Commision number
4.1.3.36
: 1,4-dihydroxy-2-naphthoyl-CoA synthase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005515
protein binding
GO:0008935
1,4-dihydroxy-2-naphthoyl-CoA synthase activity
GO:0016829
lyase activity
GO:0071890
bicarbonate binding
Biological Process
GO:0009234
menaquinone biosynthetic process
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4elx
,
PDBe:4elx
,
PDBj:4elx
PDBsum
4elx
PubMed
22606952
UniProt
P0ABU0
|MENB_ECOLI 1,4-dihydroxy-2-naphthoyl-CoA synthase (Gene Name=menB)
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