Structure of PDB 1tqy Chain G Binding Site BS01
Receptor Information
>1tqy Chain G (length=421) Species:
100226
(Streptomyces coelicolor A3(2)) [
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RRVVITGVGVRAPGGNGTRQFWELLTSGRTATRRISFFDPSPYRSQVAAE
ADFDPVAEGFGPRELDRMDRASQFAVACAREAFAASGLDPDTLDPARVGV
SLGSAVAAATSLEREYLLLSDSGRDWEVDAAWLSRHMFDYLVPSVMPAEV
AWAVGAEGPVTMVSTGCTSGLDSVGNAVRAIEEGSADVMFAGAADTPITP
IVVACFDAIRATTARNDDPEHASRPFDGTRDGFVLAEGAAMFVLEDYDSA
LARGARIHAEISGYATRCNAYHMTGLKADGREMAETIRVALDESRTDATD
IDYINAHGSGTRQNDRHETAAYKRALGEHARRTPVSSIKSMVGHSLGAIG
SLEIAACVLALEHGVVPPTANLRTSDPECDLDYVPLEARERKLRSVLTVG
SGFGGFQSAMVLRDAETAGAA
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
1tqy Chain G Residue 1098 [
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Receptor-Ligand Complex Structure
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PDB
1tqy
An antibiotic factory caught in action.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
N307 A308 E355 V401
Binding residue
(residue number reindexed from 1)
N305 A306 E353 V399
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C169 H309 E320 K341 H346 S403 F405
Catalytic site (residue number reindexed from 1)
C167 H307 E318 K339 H344 S401 F403
Enzyme Commision number
2.3.1.-
Gene Ontology
Molecular Function
GO:0004315
3-oxoacyl-[acyl-carrier-protein] synthase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
Biological Process
GO:0006633
fatty acid biosynthetic process
GO:0017000
antibiotic biosynthetic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1tqy
,
PDBe:1tqy
,
PDBj:1tqy
PDBsum
1tqy
PubMed
15286722
UniProt
Q02059
|ACTI1_STRCO Actinorhodin polyketide putative beta-ketoacyl synthase 1 (Gene Name=SCO5087)
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