MassIVE MSV000086201

Partial Public PXD021695

Repurposing chloramphenicol acetyltransferase for a robust and efficient designer ester biosynthesis platform

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Description

Repurposing chloramphenicol acetyltransferase for a robust and efficient designer ester biosynthesis platform [doi:10.25345/C55N2C] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: chloramphenicol acetyltransferase ; alcohol acyltransferase ; ester biosynthesis ; Clostridium thermocellum

Contact

Principal Investigators:
(in alphabetical order) 		Cong Trinh, University of Tennessee, Knoxville, USA
Richard J. Giannone, Oak Ridge National Laboratory, USA
Submitting User: richjg

Publications

Seo H, Lee JW, Giannone RJ, Dunlap NJ, Trinh CT.
Engineering promiscuity of chloramphenicol acetyltransferase for microbial designer ester biosynthesis.
Metab Eng. Epub 2021 Apr 16.

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Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

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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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Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct proteins quantified across all analyses (original submission and reanalyses) associated with this dataset.

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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Number of distinct proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

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.
This dataset may not contain all raw spectra data as originally deposited in PRIDE. It has been imported to MassIVE for reanalysis purposes, so its spectra data here may consist solely of processed peak lists suitable for reanalysis with most software.