Structure of PDB 7nhk Chain 4 Binding Site BS02
Receptor Information
>7nhk Chain 4 (length=53) Species:
1351
(Enterococcus faecalis) [
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AVPARRTSKAKKAKRRTHYKLTIKGLNACSNCGEMKKSHHVCPACGHYDG
KDV
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
7nhk Chain 4 Residue 101 [
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Receptor-Ligand Complex Structure
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PDB
7nhk
Structural basis of ABCF-mediated resistance to pleuromutilin, lincosamide, and streptogramin A antibiotics in Gram-positive pathogens.
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
C30 C33 C43
Binding residue
(residue number reindexed from 1)
C29 C32 C42
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003735
structural constituent of ribosome
Biological Process
GO:0006412
translation
Cellular Component
GO:0005840
ribosome
GO:0015934
large ribosomal subunit
GO:1990904
ribonucleoprotein complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7nhk
,
PDBe:7nhk
,
PDBj:7nhk
PDBsum
7nhk
PubMed
34117249
UniProt
A0A1B4XMM2
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