Structure of PDB 1o5q Chain C Binding Site BS01
Receptor Information
>1o5q Chain C (length=275) Species:
90371
(Salmonella enterica subsp. enterica serovar Typhimurium) [
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HSPGQAFRAALAKENPLQIVGAINANHALLAQRAGYQAIYLSGGGVAAGS
LGLPDLGISTLDDVLTDIRRITDVCPLPLLVDADIGFGSSAFNVARTVKS
IAKAGAAALHIEDQVAIVSKEEMVDRIRAAVDARTDPNFVIMARTDALAV
EGLEAALDRAQAYVDAGADMLFPEAITELSMYRRFADVAQVPILANITEF
GATPLFTTDELRSAHVAMALYPLSAFRAMNRAAEKVYTVLRQEGTQKNVI
DIMQTRNELYESINYYQFEEKLDAL
Ligand information
Ligand ID
PYR
InChI
InChI=1S/C3H4O3/c1-2(4)3(5)6/h1H3,(H,5,6)
InChIKey
LCTONWCANYUPML-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(=O)C(O)=O
OpenEye OEToolkits 1.7.6
CC(=O)C(=O)O
ACDLabs 12.01
O=C(C(=O)O)C
Formula
C3 H4 O3
Name
PYRUVIC ACID
ChEMBL
CHEMBL1162144
DrugBank
DB00119
ZINC
ZINC000001532517
PDB chain
1o5q Chain C Residue 3302 [
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Receptor-Ligand Complex Structure
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PDB
1o5q
Crystal structure of Salmonella typhimurium 2-methylisocitrate lyase (PrpB) and its complex with pyruvate and Mg(2+)
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
Y43 S45 G47 D85 R158
Binding residue
(residue number reindexed from 1)
Y40 S42 G44 D82 R144
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
Y43 S45 G46 G47 D58 D85 D87 H113 E115 R158 E188 N210 T217 L219
Catalytic site (residue number reindexed from 1)
Y40 S42 G43 G44 D55 D82 D84 H110 E112 R144 E174 N196 T203 L205
Enzyme Commision number
4.1.3.30
: methylisocitrate lyase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0016833
oxo-acid-lyase activity
GO:0046421
methylisocitrate lyase activity
GO:0046872
metal ion binding
GO:0140677
molecular function activator activity
Biological Process
GO:0019629
propionate catabolic process, 2-methylcitrate cycle
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1o5q
,
PDBe:1o5q
,
PDBj:1o5q
PDBsum
1o5q
PubMed
14575713
UniProt
Q56062
|PRPB_SALTY 2-methylisocitrate lyase (Gene Name=prpB)
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