Structure of PDB 1m3u Chain C Binding Site BS02
Receptor Information
>1m3u Chain C (length=262) Species:
562
(Escherichia coli) [
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PTTISLLQKYKQEKKRFATITAYDYSFAKLFADEGLNVMLVGDSLGMTVQ
GHDSTLPVTVADIAYHTAAVRRGAPNCLLLADLPFMAYATPEQAFENAAT
VMRAGANMVKIEGGEWLVETVQMLTERAVPVCGHLGLTPQSVNIFGGYKV
QGRGDEAGDQLLSDALALEAAGAQLLVLECVPVELAKRITEALAIPVIGI
GAGNVTDGQILVMHDAFGITGGHIPKFAKNFLAETGDIRAAVRQYMAEVE
SGVYPGEEHSFH
Ligand information
Ligand ID
KPL
InChI
InChI=1S/C6H10O4/c1-6(2,3-7)4(8)5(9)10/h7H,3H2,1-2H3,(H,9,10)
InChIKey
PKVVTUWHANFMQC-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)(CO)C(=O)C(=O)O
ACDLabs 10.04
O=C(O)C(=O)C(C)(C)CO
CACTVS 3.341
CC(C)(CO)C(=O)C(O)=O
Formula
C6 H10 O4
Name
KETOPANTOATE;
2-DEHYDROPANTOATE
ChEMBL
DrugBank
DB03795
ZINC
ZINC000001532800
PDB chain
1m3u Chain C Residue 265 [
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Receptor-Ligand Complex Structure
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PDB
1m3u
Structure of E. coli Ketopantoate Hydroxymethyl Transferase Complexed with Ketopantoate and Mg(2+), Solved by Locating 160 Selenomethionine Sites.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
L42 G44 D45 S46 K112 H136 E181 I212
Binding residue
(residue number reindexed from 1)
L40 G42 D43 S44 K110 H134 E179 I210
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.2.11
: 3-methyl-2-oxobutanoate hydroxymethyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003864
3-methyl-2-oxobutanoate hydroxymethyltransferase activity
GO:0016740
transferase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0015940
pantothenate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1m3u
,
PDBe:1m3u
,
PDBj:1m3u
PDBsum
1m3u
PubMed
12906829
UniProt
P31057
|PANB_ECOLI 3-methyl-2-oxobutanoate hydroxymethyltransferase (Gene Name=panB)
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