Structure of PDB 5cdp Chain D Binding Site BS02
Receptor Information
>5cdp Chain D (length=189) Species:
158879
(Staphylococcus aureus subsp. aureus N315) [
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KLADCSSKSPEECEIFLVEGDSAGGSTKSGRDSRTQAILPLRGKILNVEK
ARLDRILNNNEIRQMITAFGTGIGGDFDLAKARYHKIVIMTDADVDGAHI
RTLLLTFFYRFMRPLIEAGYVYIAQPPTGYKGLGEMNADQLWETTMNPEH
RALLQVKLEDAIEADQTFEMLMGDVVENRRQFIEDNAVY
Ligand information
>5cdp Chain F (length=8) [
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agccgtag
Receptor-Ligand Complex Structure
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PDB
5cdp
Structural basis of DNA gyrase inhibition by antibacterial QPT-1, anticancer drug etoposide and moxifloxacin.
Resolution
2.45 Å
Binding residue
(original residue number in PDB)
G459 K460 D512
Binding residue
(residue number reindexed from 1)
G43 K44 D96
Enzymatic activity
Enzyme Commision number
5.6.2.2
: DNA topoisomerase (ATP-hydrolyzing).
Gene Ontology
Molecular Function
GO:0003677
DNA binding
GO:0003918
DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity
GO:0005524
ATP binding
Biological Process
GO:0006265
DNA topological change
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Molecular Function
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Biological Process
External links
PDB
RCSB:5cdp
,
PDBe:5cdp
,
PDBj:5cdp
PDBsum
5cdp
PubMed
26640131
UniProt
P66937
|GYRB_STAAN DNA gyrase subunit B (Gene Name=gyrB)
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