Structure of PDB 1jpm Chain A Binding Site BS01
Receptor Information
>1jpm Chain A (length=359) Species:
1423
(Bacillus subtilis) [
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MKIIRIETSRIAVPLTKPFKTALRTVYTAESVIVRITYDSGAVGWGEAPP
TLVITGDSMDSIESAIHHVLKPALLGKSLAGYEAILHDIQHLLTGNMSAK
AAVEMALYDGWAQMCGLPLYQMLGGYRDTLETDYTVSVNSPEEMAADAEN
YLKQGFQTLKIKVGKDDIATDIARIQEIRKRVGSAVKLRLDANQGWRPKE
AVTAIRKMEDAGLGIELVEQPVHKDDLAGLKKVTDATDTPIMADESVFTP
RQAFEVLQTRSADLINIKLMKAGGISGAEKINAMAEACGVECMVGSMIET
KLGITAAAHFAASKRNITRFDFDAPLMLKTDVFNGGITYSGSTISMPGKP
GLGIIGAAL
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
1jpm Chain A Residue 1003 [
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Receptor-Ligand Complex Structure
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PDB
1jpm
Evolution of enzymatic activities in the enolase superfamily: crystal structures of the L-Ala-D/L-Glu epimerases from Escherichia coli and Bacillus subtilis.
Resolution
2.25 Å
Binding residue
(original residue number in PDB)
D191 E219 D244
Binding residue
(residue number reindexed from 1)
D191 E219 D244
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F19 P50 V53 T135 K160 K162 L190 D191 A192 N193 E219 D244 E245 S246 N266 K268 G295 S296 M297 F320 D321 F322
Catalytic site (residue number reindexed from 1)
F19 P50 V53 T135 K160 K162 L190 D191 A192 N193 E219 D244 E245 S246 N266 K268 G295 S296 M297 F320 D321 F322
Enzyme Commision number
5.1.1.20
: L-Ala-D/L-Glu epimerase.
Gene Ontology
Molecular Function
GO:0016853
isomerase activity
GO:0016854
racemase and epimerase activity
GO:0016855
racemase and epimerase activity, acting on amino acids and derivatives
GO:0046872
metal ion binding
GO:0103031
L-Ala-D/L-Glu epimerase activity
Biological Process
GO:0016998
cell wall macromolecule catabolic process
GO:0071555
cell wall organization
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1jpm
,
PDBe:1jpm
,
PDBj:1jpm
PDBsum
1jpm
PubMed
11747448
UniProt
O34508
|AEEP_BACSU L-Ala-D/L-Glu epimerase (Gene Name=ykfB)
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