Structure of PDB 1mra Chain A Binding Site BS01
Receptor Information
>1mra Chain A (length=357) Species:
303
(Pseudomonas putida) [
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EVLITGLRTRAVNVPLAYPVHTAVGTVGTAPLVLIDLATSAGVVGHSYLF
AYTPVALKSLKQLLDDMAAMIVNEPLAPVSLEAMLAKRFCLAGYTGLIRM
AAAGIDMAAWDALGKVHETPLVKLLGANARPVQAYDSHSLDGVKLATERA
VTAAELGFRAVKTKIGYPALDQDLAVVRSIRQAVGDDFGIMVDYNQSLDV
PAAIKRSQALQQEGVTWIEEPTLQHDYEGHQRIQSKLNVPVQMGENWLGP
EEMFKALSIGACRLAMPNAMKIGGVTGWIRASALAQQFGIPMSSHLFQEI
SAHLLAATPTAHWLERLDLAGSVIEPTLTFEGGNAVIPDLPGVGIIWREK
EIGKYLV
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
1mra Chain A Residue 360 [
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Receptor-Ligand Complex Structure
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PDB
1mra
Mechanism of the reaction catalyzed by mandelate racemase: structure and mechanistic properties of the D270N mutant.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
D195 E221 E247
Binding residue
(residue number reindexed from 1)
D193 E219 E245
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
V22 S139 K164 K166 D195 N197 E221 G246 E247 N270 H297 L298 F299 E317
Catalytic site (residue number reindexed from 1)
V20 S137 K162 K164 D193 N195 E219 G244 E245 N268 H295 L296 F297 E315
Enzyme Commision number
5.1.2.2
: mandelate racemase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016836
hydro-lyase activity
GO:0016853
isomerase activity
GO:0018838
mandelate racemase activity
GO:0046872
metal ion binding
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
GO:0018924
mandelate metabolic process
GO:0019596
mandelate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1mra
,
PDBe:1mra
,
PDBj:1mra
PDBsum
1mra
PubMed
8639525
UniProt
P11444
|MANR_PSEPU Mandelate racemase (Gene Name=mdlA)
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