Skip to Main Content (Press Enter)

Logo CNR
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills

UNI-FIND
Logo CNR

|

UNI-FIND

cnr.it
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills
  1. Outputs

Structural and functional characterization of TgpA, a critical protein for the viability of Pseudomonas aeruginosa

Academic Article
Publication Date:
2019
abstract:
Pseudomonas aeruginosa is an opportunistic pathogen associated with severe diseases, such as cystic fibrosis. During an extensive search for novel essential genes, we identified tgpA (locus PA2873) in P. aeruginosa PAO1, as a gene playing a critical role in bacterial viability. TgpA, the translated protein, is an internal membrane protein with a periplasmic soluble domain, predicted to be endowed with a transglutaminase-like fold, hosting the Cys404, His448, and Asp464 triad. We report here that Cys404 mutation hampers the essential role of TgpA in granting P. aeruginosa viability. Moreover, we present the crystal structure of the TgpA periplasmic domain at 1.6 angstrom resolution as a first step towards structure-activity analysis of a new potential target for the discovery of antibacterial compounds.
Iris type:
01.01 Articolo in rivista
Keywords:
Periplasmic proteins; X-ray crystallography; Antibacterials; Point mutations; Heterologous expression; Cystic fibrosis; Peptidoglycans
List of contributors:
MILANI DE MAYO DE MARI, Mario; Mastrangelo, Eloise
Authors of the University:
MASTRANGELO ELOISE
MILANI DE MAYO DE MARI MARIO
Handle:
https://iris.cnr.it/handle/20.500.14243/388342
Published in:
JOURNAL OF STRUCTURAL BIOLOGY
Journal
  • Use of cookies

Powered by VIVO | Designed by Cineca | 26.5.0.0 | Sorgente dati: PREPROD (Ribaltamento disabilitato)