Structure of PDB 8xt0 Chain LR Binding Site BS02
Receptor Information
>8xt0 Chain LR (length=146) Species:
9606
(Homo sapiens) [
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EVDPVENEAVAPEFTNRNPRNLELLSVARKERGWRTVFPSREFWHRLRVI
RTQHHVEALVEHQNGKVVVSASTREWAIKKHLYSTRNVVACESIGRVLAQ
RCLEAGINFMVYQPTPWEAASDSMKRLQSAMTEGGVVLREPQRIYE
Ligand information
>8xt0 Chain L2 (length=56) [
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agaguguagcuuaaaagcacccaacuuacacuuaggagauucaauugacg
cucuga
<<<<<...<<<....>>>.<<.<<.......>>.>>....<<<..>>>.>
>>>>..
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)
T85 Q86 H87 H88 R107 N120 V121 W150 S154 S156
Binding residue
(residue number reindexed from 1)
T52 Q53 H54 H55 R74 N87 V88 W117 S121 S123
Gene Ontology
Cellular Component
GO:0005737
cytoplasm
GO:0005840
ribosome
GO:1990904
ribonucleoprotein complex
View graph for
Cellular Component
External links
PDB
RCSB:8xt0
,
PDBe:8xt0
,
PDBj:8xt0
PDBsum
8xt0
PubMed
38942792
UniProt
A8K9D2
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