Structure of PDB 5fjt Chain A Binding Site BS02
Receptor Information
>5fjt Chain A (length=367) Species:
37632
(Amycolatopsis sp.) [
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MKLSGVELRRVQMPLVAPFRTSFGTQSVRELLLLRAVTPAGEGWGECVTM
AGPLYSSEYNDGAEHVLRHYLIPALLAAEDITAAKVTPLLAKFKGHRMAK
GALEMAVLDAELRAHERSFAAELGSVRDSVPCGVSVGIMDTIPQLLDVVG
GYLDEGYVRIKLKIEPGWDVEPVRAVRERFGDDVLLQVDANTAYTLGDAP
QLARLDPFGLLLIEQPLEEEDVLGHAELARRIQTPICLDESIVSARAAAD
AIKLGAVQIVNIKPGRVGGYLEARRVHDVCAAHGIPVWCGDMIETGLGRA
ANVALASLPNFTLPGDTSASDRYYKTDITEPFVLSGGHLPVPTGPGLGVA
PIPELLDEVTTAKVWIG
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
5fjt Chain A Residue 1369 [
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Receptor-Ligand Complex Structure
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PDB
5fjt
Structure of N-Acylamino Acid Racemase Mutants in Complex with Substrates
Resolution
2.11 Å
Binding residue
(original residue number in PDB)
D189 E214 D239
Binding residue
(residue number reindexed from 1)
D189 E214 D239
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F19 S135 K161 K163 D189 N191 E214 D239 E240 S241 K263 G290 D291 M292 G315 D316 T317
Catalytic site (residue number reindexed from 1)
F19 S135 K161 K163 D189 N191 E214 D239 E240 S241 K263 G290 D291 M292 G315 D316 T317
Enzyme Commision number
4.2.1.113
: o-succinylbenzoate synthase.
5.1.1.-
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0016853
isomerase activity
GO:0043748
O-succinylbenzoate synthase activity
GO:0046872
metal ion binding
Biological Process
GO:0009234
menaquinone biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5fjt
,
PDBe:5fjt
,
PDBj:5fjt
PDBsum
5fjt
PubMed
UniProt
Q44244
|NSAR_AMYSP N-succinylamino acid racemase (Gene Name=Aaar)
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