Structure of PDB 1zfn Chain A Binding Site BS01
Receptor Information
>1zfn Chain A (length=244) Species:
562
(Escherichia coli) [
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MNDRDFMRYSRQILLDDIALDGQQKLLDSQVLIIGLGGLGTPAALYLAGA
GVGTLVLADDDDVHLSNLQRQILFTTEDIDRPKSQVSQQRLTQLNPDIQL
TALQQRLTGEALKDAVARADVVLDCTDNMATRQEINAACVALNTPLITAS
AVGFGGQLMVLTPPWEQGCYRCLWPDNQEPERNCRTAGVVGPVVGVMGTL
QALEAIKLLSGIETPAGELRLFDGKSSQWRSLALRRASGCPVCG
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
1zfn Chain A Residue 252 [
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Receptor-Ligand Complex Structure
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PDB
1zfn
Structural Analysis of Escherichia Coli ThiF.
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
C169 C172 C240 C243
Binding residue
(residue number reindexed from 1)
C169 C172 C240 C243
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R11 D127
Catalytic site (residue number reindexed from 1)
R11 D127
Enzyme Commision number
2.7.7.73
: sulfur carrier protein ThiS adenylyltransferase.
Gene Ontology
Molecular Function
GO:0004792
thiosulfate sulfurtransferase activity
GO:0005524
ATP binding
GO:0008146
sulfotransferase activity
GO:0008270
zinc ion binding
GO:0008641
ubiquitin-like modifier activating enzyme activity
GO:0016779
nucleotidyltransferase activity
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0070733
AMPylase activity
Biological Process
GO:0009228
thiamine biosynthetic process
GO:0009229
thiamine diphosphate biosynthetic process
GO:0052837
thiazole biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:1902503
adenylyltransferase complex
GO:1990228
sulfurtransferase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1zfn
,
PDBe:1zfn
,
PDBj:1zfn
PDBsum
1zfn
PubMed
15896804
UniProt
P30138
|THIF_ECOLI Sulfur carrier protein ThiS adenylyltransferase (Gene Name=thiF)
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