Structure of PDB 1g67 Chain B Binding Site BS01

Receptor Information
>1g67 Chain B (length=225) Species: 1423 (Bacillus subtilis) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GIRMTRISREMMKELLSVYFIMGSNNTKADPVTVVQKALKGGATLYQFRE
KGGDALTGEARIKFAEKAQAACREAGVPFIVNDDVELALNLKADGIHIGQ
EDANAKEVRAAIGDMILGVAAHTMSEVKQAEEDGADYVGLGPIYPTETKK
DTRAVQGVSLIEAVRRQGISIPIVGIGGITIDNAAPVIQAGADGVSMISA
ISQAEDPESAARKFREEIQTYKTGR
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 chain1g67 Chain B Residue 2008 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1g67 Structural characterization of the enzyme-substrate, enzyme-intermediate, and enzyme-product complexes of thiamin phosphate synthase.
Resolution1.4 Å
Binding residue
(original residue number in PDB)
D1093 D1112
Binding residue
(residue number reindexed from 1)
D83 D102
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) R1059 A1130 K1159
Catalytic site (residue number reindexed from 1) R49 A120 K149
Enzyme Commision number 2.5.1.3: thiamine phosphate synthase.
Gene Ontology
Molecular Function
GO:0000287 magnesium ion binding
GO:0004789 thiamine-phosphate diphosphorylase activity
GO:0016740 transferase activity
GO:0046872 metal ion binding
Biological Process
GO:0009228 thiamine biosynthetic process
GO:0009229 thiamine diphosphate biosynthetic process
Cellular Component
GO:0005737 cytoplasm

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Cellular Component
External links
PDB RCSB:1g67, PDBe:1g67, PDBj:1g67
PDBsum1g67
PubMed11513589
UniProtP39594|THIE_BACSU Thiamine-phosphate synthase (Gene Name=thiE)

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