Structure of PDB 2ps2 Chain C Binding Site BS01
Receptor Information
>2ps2 Chain C (length=361) Species:
510516
(Aspergillus oryzae RIB40) [
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DLKIARIDVFQVDLPYSGGVYYLSFDATIVRITTDTGIEGWGESTPFGSN
YIASHPRGVRAGIATMAPSLIGLDPRRVDRINDAMDDALLGHEDAKTAID
VACWDIFGKSVGLPVCELLGGRTNTRLPLISSIYVGEPEDMRARVAKYRA
KGYKGQSVKISGEPVTDAKRITAALANQQPDEFFIVDANGKLSVETALRL
LRLLPHGLDFALEAPCATWRECISLRRKTDIPIIYDELATNEMSIVKILA
DDAAEGIDLKISKAGGLTRGRRQRDICLAAGYSVSVQETCGSDIAFAAIV
HLAQTIPERSLRCILECRDMVTVKTADGAFDIQDGFATAPTTPGLGIMPR
LDVLGEAVASY
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
2ps2 Chain C Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
2ps2
Crystal structure of putative mandelate racemase/muconate lactonizing enzyme from Aspergillus oryzae.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D196 E222 D245
Binding residue
(residue number reindexed from 1)
D187 E213 D236
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
Y23 S141 Q165 S166 V167 K168 D196 E222 D245 E246 K269 Q296 E297 T298 C322 I323 L324
Catalytic site (residue number reindexed from 1)
Y21 S132 Q156 S157 V158 K159 D187 E213 D236 E237 K260 Q287 E288 T289 C313 I314 L315
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0016854
racemase and epimerase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:2ps2
,
PDBe:2ps2
,
PDBj:2ps2
PDBsum
2ps2
PubMed
UniProt
Q2U1E8
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