8GXJ

Pseudomonas aeruginosa N-acetyltransferase domain-containing protein PA3270

Summary for 8GXJ

• Entry DOI: 10.2210/pdb8gxj/pdb
• Descriptor: N-acetyltransferase domain-containing protein (2 entities in total)
• Functional Keywords: apo-form of pa3270, transferase, acetyltransferase
• Biological source: Pseudomonas aeruginosa PAO1
• Total number of polymer chains: 4
• Total formula weight: 87720.91

Authors

Song, Y.J.,Bao, R. (deposition date: 2022-09-20, release date: 2022-10-12, Last modification date: 2023-11-08)

Primary citation

Song, Y.,Zhang, S.,Ye, Z.,Song, Y.,Chen, L.,Tong, A.,He, Y.,Bao, R.
The novel type II toxin-antitoxin PacTA modulates Pseudomonas aeruginosa iron homeostasis by obstructing the DNA-binding activity of Fur.
Nucleic Acids Res., 50:10586-10600, 2022

PubMed Abstract: Type II toxin-antitoxin (TA) systems are widely distributed in bacterial and archaeal genomes and are involved in diverse critical cellular functions such as defense against phages, biofilm formation, persistence, and virulence. GCN5-related N-acetyltransferase (GNAT) toxin, with an acetyltransferase activity-dependent mechanism of translation inhibition, represents a relatively new and expanding family of type II TA toxins. We here describe a group of GNAT-Xre TA modules widely distributed among Pseudomonas species. We investigated PacTA (one of its members encoded by PA3270/PA3269) from Pseudomonas aeruginosa and demonstrated that the PacT toxin positively regulates iron acquisition in P. aeruginosa. Notably, other than arresting translation through acetylating aminoacyl-tRNAs, PacT can directly bind to Fur, a key ferric uptake regulator, to attenuate its DNA-binding affinity and thus permit the expression of downstream iron-acquisition-related genes. We further showed that the expression of the pacTA locus is upregulated in response to iron starvation and the absence of PacT causes biofilm formation defect, thereby attenuating pathogenesis. Overall, these findings reveal a novel regulatory mechanism of GNAT toxin that controls iron-uptake-related genes and contributes to bacterial virulence.

PubMed: 36200834
DOI: 10.1093/nar/gkac867

Experimental method

X-RAY DIFFRACTION (2.18 Å)