Structure of PDB 1oy0 Chain E Binding Site BS01

Receptor Information
>1oy0 Chain E (length=248) Species: 1773 (Mycobacterium tuberculosis) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
RTKIRTHHLQRWKADGHKWAMLTAYDYSTARIFDEAGIPVLLVGDSAANV
VYGYDTTVPISIDELIPLVRGVVRGAPHALVVADLPFGSYEAGPTAALAA
ATRFLKDGGAHAVKLEGGERVAEQIACLTAAGIPVMAHIGFTPGDAAEQT
IADAIAVAEAGAFAVVMEMVPAELATQITGKLTIPTVGIGAGPNCDGQVL
VWQDMAGFSGAKTARFVKRYADVGGELRRAAMQYAQEVAGGVFPADEH
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain1oy0 Chain E Residue 905 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1oy0 The Crystal Structure of the First Enzyme in the Pantothenate Biosynthetic Pathway, Ketopantoate Hydroxymethyltransferase, from M. tuberculosis
Resolution2.8 Å
Binding residue
(original residue number in PDB)
D62 E133
Binding residue
(residue number reindexed from 1)
D45 E116
Annotation score1
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:0046872 metal ion binding
Biological Process
GO:0015940 pantothenate biosynthetic process
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:1oy0, PDBe:1oy0, PDBj:1oy0
PDBsum1oy0
PubMed12842039
UniProtP9WIL7|PANB_MYCTU 3-methyl-2-oxobutanoate hydroxymethyltransferase (Gene Name=panB)

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