MassIVE MSV000092175

Partial Public PXD043024

The twin-arginine translocation system of Achromobacter xylosoxidans

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Description

Achromobacter xylosoxidans is an emerging pathogen, causing airway infections in patients with cystic fibrosis (CF). The knowledge about virulence factors and protein secretion systems in this bacterium is limited. The twin-arginine translocation (Tat) is a protein secretion system for the transportation of folded proteins across the inner cell membrane of Gram-negative bacteria. Here, we report a quantitative proteome analysis of fractionated Achromobacter xylosoxidans wt and Tat-mutant cells in iron-containing and iron-lacking conditions. [doi:10.25345/C5CR5NP3P] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Achromobacter xylosoxidans, cystic fibrosis, twin-arginine translocation system, fractionated wt and Tat-mutant cells, iron

Contact

Principal Investigators:
(in alphabetical order) 		Lisa Pahlman, Lund University, Sweden
Submitting User: LJOksanenHapponen
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Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

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Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

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A protein is differentially abundant if its change in abundance across conditions is found to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated with statistical tests for differential abundance.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
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