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5WPH

Crystal structure of ArsN, N-acetyltransferase with substrate AST from Pseudomonas putida KT2440

Summary for 5WPH
Entry DOI10.2210/pdb5wph/pdb
DescriptorPhosphinothricin N-acetyltransferase, (2S)-2-amino-4-[hydroxy(methyl)arsoryl]butanoic acid, SODIUM ION, ... (4 entities in total)
Functional Keywordsn-acetyltransferase, pseudomonas putida, transferase
Biological sourcePseudomonas putida
Total number of polymer chains6
Total formula weight140829.98
Authors
Venkadesh, S.,Dheeman, D.S.,Yoshinaga, M.,Kandavelu, P.,Rosen, B.P. (deposition date: 2017-08-04, release date: 2018-10-10, Last modification date: 2023-10-04)
Primary citationNadar, V.S.,Chen, J.,Dheeman, D.S.,Galvan, A.E.,Yoshinaga-Sakurai, K.,Kandavelu, P.,Sankaran, B.,Kuramata, M.,Ishikawa, S.,Rosen, B.P.,Yoshinaga, M.
Arsinothricin, an arsenic-containing non-proteinogenic amino acid analog of glutamate, is a broad-spectrum antibiotic.
Commun Biol, 2:131-131, 2019
Cited by
PubMed Abstract: The emergence and spread of antimicrobial resistance highlights the urgent need for new antibiotics. Organoarsenicals have been used as antimicrobials since Paul Ehrlich's salvarsan. Recently a soil bacterium was shown to produce the organoarsenical arsinothricin. We demonstrate that arsinothricin, a non-proteinogenic analog of glutamate that inhibits glutamine synthetase, is an effective broad-spectrum antibiotic against both Gram-positive and Gram-negative bacteria, suggesting that bacteria have evolved the ability to utilize the pervasive environmental toxic metalloid arsenic to produce a potent antimicrobial. With every new antibiotic, resistance inevitably arises. The gene, widely distributed in bacterial arsenic resistance () operons, selectively confers resistance to arsinothricin by acetylation of the α-amino group. Crystal structures of ArsN1 -acetyltransferase, with or without arsinothricin, shed light on the mechanism of its substrate selectivity. These findings have the potential for development of a new class of organoarsenical antimicrobials and ArsN1 inhibitors.
PubMed: 30993215
DOI: 10.1038/s42003-019-0365-y
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.19 Å)
Structure validation

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