MassIVE MSV000086241

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Quantitative Proteomics Reveals UGA-independent Mis-incorporation of Selenocysteine throughout Escherichia coli Proteome

Description

LC-MS/MS based shotgun proteomics data of E. coli grew in standard M9 minimal medium, sulfur-depleted medium and selenite medium. We detected selenocysteine mis-incorporation in selenite group and compared its proteome changes with M9 and sulfur-depleted group. Files beginning with letter M, N and S are data sets of M9, sulfur-depleted, and selenite group, respectively. There are 4 biological replicates in each group, and 3 technical replicates in each biological replicate. [doi:10.25345/C5878F] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: selenocysteine ; misincorporation

Contact

Principal Investigators:
(in alphabetical order)
Hao Chunlin, HKUST, China
Henry Lam, HKUST, China
Submitting User: ustlin

Publications

Chunlin Hao and Henry H. N. Lam.
Quantitative Proteomics Reveals UGA-Independent Misincorporation of Selenocysteine throughout the Escherichia coli Proteome.
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Identification Results
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Number of distinct biological replicates 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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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.

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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.

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