Structure of PDB 2gge Chain A Binding Site BS01
Receptor Information
>2gge Chain A (length=373) Species:
1423
(Bacillus subtilis) [
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LVKIVRIETFPLFHRLEKPYGDANGFKRYRTCYLIRIITESGIDGWGECV
DWLPALHVGFTKRIIPFLLGKQAGSRLSLVRTIQKWHQRAASAVSMALTE
IAAKAADCSVCELWGGRYREEIPVYASFQSYSDSPQWISRSVSNVEAQLK
KGFEQIKVKIGGTSFKEDVRHINALQHTAGSSITMILDANQSYDAAAAFK
WERYFSEWTNIGWLEEPLPFDQPQDYAMLRSRLSVPVAGGENMKGPAQYV
PLLSQRCLDIIQPDVMHVNGIDEFRDCLQLARYFGVRASAHAYDGSLSRL
YALFAQACLPPWSKMKNDHIEPIEWDVMENPFTDLVSLQPSKGMVHIPKG
KGIGTEINMEIVNRYKWDGSAYE
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
2gge Chain A Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
2gge
Crystal Structure of Mandelate Racemase/Muconate Lactonizing Enzyme from Bacillus Subtilis complexed with MG++ at 1.8 A
Resolution
1.89 Å
Binding residue
(original residue number in PDB)
E217 E243 H293
Binding residue
(residue number reindexed from 1)
E215 E241 H291
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
Y22 S129 K159 K161 D190 N192 E217 G242 E243 D266 H293 N319 D320 E326
Catalytic site (residue number reindexed from 1)
Y20 S127 K157 K159 D188 N190 E215 G240 E241 D264 H291 N317 D318 E324
Enzyme Commision number
5.-.-.-
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016836
hydro-lyase activity
GO:0016853
isomerase activity
GO:0046872
metal ion binding
Biological Process
GO:0016052
carbohydrate catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:2gge
,
PDBe:2gge
,
PDBj:2gge
PDBsum
2gge
PubMed
UniProt
O06741
|YITF_BACSU Putative isomerase YitF (Gene Name=yitF)
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