Structure of PDB 3cxo Chain B Binding Site BS01
Receptor Information
>3cxo Chain B (length=402) Species:
99287
(Salmonella enterica subsp. enterica serovar Typhimurium str. LT2) [
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IMTLPKIKHVRAWFIGGATAEKGAGGGDYHDQGGNHWIDDHIATPMSKYR
DYEQSRQSFGINVLGTLIVEVEAENRQTGFAVSTAGEMGCFIVEKHLNRF
IEGKCVSDIKLIHDQMLGATMYYSGSGGLVMNTISCVDLALWDLFGKVVG
LPVYKLLGGAVRDEIQFYATGARPDLAKEMGFIGGKMPTHWGPHDGDAGI
RKDAAMVADMREKCGPDFWLMLDCWMSQDVNYATKLAHACAPFNLKWIEE
CLPPQQYEGYRELKRNAPAGMMVTSGEHHGTLQSFRTLAETGIDIMQPDV
GWCGGLTTLVEIAALAKSRGQLVVPHGSSVYSHHAVITFTNTPFSEFLMT
SPDCSTLRPQFDPILLDEPVPVNGRIHKSVLDKPGFGVELNRDCHLKRPY
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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
3cxo Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
3cxo
Evolution of enzymatic activities in the enolase superfamily: L-rhamnonate dehydratase.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D226 E252 E280
Binding residue
(residue number reindexed from 1)
D223 E249 E277
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)
Y52 K186 P188 G192 H194 A198 D223 W225 E249 T274 G276 E277 Q297 D299 H326 E346 S351
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:3cxo
,
PDBe:3cxo
,
PDBj:3cxo
PDBsum
3cxo
PubMed
18754693
UniProt
Q8ZNF9
|RHMD_SALTY L-rhamnonate dehydratase (Gene Name=rhmD)
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