Structure of PDB 2gsh Chain A Binding Site BS01
Receptor Information
>2gsh Chain A (length=403) Species:
99287
(Salmonella enterica subsp. enterica serovar Typhimurium str. LT2) [
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NIMTLPKIKHVRAWFIGGATAEKGAGGGDYHDQGGNHWIDDHIATPMSKY
RDYEQSRQSFGINVLGTLIVEVEAENRQTGFAVSTAGEMGCFIVEKHLNR
FIEGKCVSDIKLIHDQMLGATMYYSGSGGLVMNTISCVDLALWDLFGKVV
GLPVYKLLGGAVRDEIQFYATGARPDLAKEMGFIGGKMPTHWGPHDGDAG
IRKDAAMVADMREKCGPDFWLMLDCWMSQDVNYATKLAHACAPFNLKWIE
ECLPPQQYEGYRELKRNAPAGMMVTSGEHHGTLQSFRTLAETGIDIMQPD
VGWCGGLTTLVEIAALAKSRGQLVVPHGSSVYSHHAVITFTNTPFSEFLM
TSPDCSTLRPQFDPILLDEPVPVNGRIHKSVLDKPGFGVELNRDCHLKRP
YSH
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
2gsh Chain A Residue 414 [
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Receptor-Ligand Complex Structure
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PDB
2gsh
Crystal Structure of L-rhamnonate dehydratase from Salmonella Typhimurium Lt2
Resolution
2.393 Å
Binding residue
(original residue number in PDB)
D226 E252 E280
Binding residue
(residue number reindexed from 1)
D224 E250 E278
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y55 K189 P191 G195 H197 A201 D226 W228 E252 T277 G279 E280 Q300 D302 H329 E349 S354
Catalytic site (residue number reindexed from 1)
Y53 K187 P189 G193 H195 A199 D224 W226 E250 T275 G277 E278 Q298 D300 H327 E347 S352
Enzyme Commision number
4.2.1.90
: L-rhamnonate dehydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016829
lyase activity
GO:0016836
hydro-lyase activity
GO:0046872
metal ion binding
GO:0050032
L-rhamnonate dehydratase activity
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:2gsh
,
PDBe:2gsh
,
PDBj:2gsh
PDBsum
2gsh
PubMed
UniProt
Q8ZNF9
|RHMD_SALTY L-rhamnonate dehydratase (Gene Name=rhmD)
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