Structure of PDB 3op2 Chain A Binding Site BS01
Receptor Information
>3op2 Chain A (length=375) Species:
518
(Bordetella bronchiseptica) [
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SLKITEVKAHALSTPIPERMRVESGAGLKLNRQMILVEVRTDEGVTGVGS
PSGPYDLAVLKRAIEDVIGPQLIGEDPANINYLWHKVFHGEVSRSVGIAA
MSGVDIALWDLKGRAMNQPIYQLLGGKFHTRGVRAYASSIYWDLTPDQAA
DELAGWVEQGFTAAKLKVGRAPRKDAANLRAMRQRVGADVEILVDANQSL
GRHDALAMLRILDEAGCYWFEEPLSIDDIEGHRILRAQGTPVRIATGENL
YTRNAFNDYIRNDAIDVLQADASRAGGITEALAISASAASAHLAWNPHTF
NDIITVAANLHLVAASPHPAMFEWDITHNDLMTRLASYDLKLENGLVQPP
QGPGLGFEIDWDFVAAHAWKGEPAI
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
3op2 Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
3op2
Crystal structure of putative mandelate racemase from Bordetella bronchiseptica RB50 complexed with 2-oxoglutarate/phosphate
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D201 E227 E254
Binding residue
(residue number reindexed from 1)
D195 E221 E248
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
M21 G54 D57 S144 K171 K173 D201 N203 E227 G253 E254 N255 Q275 D277 H304 T305 F306 E329 I332 H334
Catalytic site (residue number reindexed from 1)
M20 G53 D56 S138 K165 K167 D195 N197 E221 G247 E248 N249 Q269 D271 H298 T299 F300 E323 I326 H328
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016836
hydro-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3op2
,
PDBe:3op2
,
PDBj:3op2
PDBsum
3op2
PubMed
UniProt
A0A0H3LT39
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