Structure of PDB 8xt0 Chain Sa Binding Site BS02
Receptor Information
>8xt0 Chain Sa (length=162) Species:
9606
(Homo sapiens) [
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PMKGRFPIRRTLQYLSQGNVVFKDSVKVMTVNYNTHGELGEGARKFVFFN
IPQIQYKNPWVQIMMFKNMTPSPFLRFYLDSGEQVLVDVETKSNKEIMEH
IRKILGKNEETLREEEEEKKQLSHPANFGPRKYCLRECICEVEGQVPCPS
LVPLPKEMRGKY
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
8xt0 Chain Sa Residue 200 [
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Receptor-Ligand Complex Structure
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PDB
8xt0
Structural basis for differential inhibition of eukaryotic ribosomes by tigecycline.
Resolution
3.2 Å
Binding residue
(original residue number in PDB)
C141 C149
Binding residue
(residue number reindexed from 1)
C140 C148
Annotation score
4
Gene Ontology
Molecular Function
GO:0003735
structural constituent of ribosome
Biological Process
GO:0032543
mitochondrial translation
Cellular Component
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
GO:0005763
mitochondrial small ribosomal subunit
GO:0005840
ribosome
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:8xt0
,
PDBe:8xt0
,
PDBj:8xt0
PDBsum
8xt0
PubMed
38942792
UniProt
P82663
|RT25_HUMAN Small ribosomal subunit protein mS25 (Gene Name=MRPS25)
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