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8C8U

Priestia megaterium mupirocin-resistant isoleucyl-tRNA synthetase 2 complexed with mupirocin

Summary for 8C8U
Entry DOI10.2210/pdb8c8u/pdb
DescriptorIsoleucine--tRNA ligase, ZINC ION, MUPIROCIN, ... (6 entities in total)
Functional Keywordsantibiotic, mupirocin-resistant, ilers2, rna-binding, mupirocin, rna binding protein
Biological sourcePriestia megaterium
Total number of polymer chains1
Total formula weight119091.85
Authors
Brkic, A.,Leibundgut, M.,Jablonska, J.,Zanki, V.,Car, Z.,Petrovic Perokovic, V.,Gruic-Sovulj, I.,Ban, N. (deposition date: 2023-01-21, release date: 2023-08-23, Last modification date: 2024-03-27)
Primary citationBrkic, A.,Leibundgut, M.,Jablonska, J.,Zanki, V.,Car, Z.,Petrovic Perokovic, V.,Marsavelski, A.,Ban, N.,Gruic-Sovulj, I.
Antibiotic hyper-resistance in a class I aminoacyl-tRNA synthetase with altered active site signature motif.
Nat Commun, 14:5498-5498, 2023
Cited by
PubMed Abstract: Antibiotics target key biological processes that include protein synthesis. Bacteria respond by developing resistance, which increases rapidly due to antibiotics overuse. Mupirocin, a clinically used natural antibiotic, inhibits isoleucyl-tRNA synthetase (IleRS), an enzyme that links isoleucine to its tRNA for protein synthesis. Two IleRSs, mupirocin-sensitive IleRS1 and resistant IleRS2, coexist in bacteria. The latter may also be found in resistant Staphylococcus aureus clinical isolates. Here, we describe the structural basis of mupirocin resistance and unravel a mechanism of hyper-resistance evolved by some IleRS2 proteins. We surprisingly find that an up to 10-fold increase in resistance originates from alteration of the HIGH motif, a signature motif of the class I aminoacyl-tRNA synthetases to which IleRSs belong. The structural analysis demonstrates how an altered HIGH motif could be adopted in IleRS2 but not IleRS1, providing insight into an elegant mechanism for coevolution of the key catalytic motif and associated antibiotic resistance.
PubMed: 37679387
DOI: 10.1038/s41467-023-41244-3
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.901 Å)
Structure validation

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数据于2024-11-06公开中

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