MassIVE MSV000093876

Complete Public PXD048612

Ho_BLM_TOP3A_RMI_BioID_P130_Velos_Elite

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Description

This dataset consists of 25 raw MS files and associated peak lists and results files, acquired on a Thermo LTQ Velos Pro or Thermo Orbitrap Elite mass spectrometer operated in Data Dependent Acquisition mode. Samples were generated by Edith Cheng. Affinity purifications and mass spectrometry acquisition was performed by Wade Dunham. Analysis was performed by Jennifer Ho, Wade Dunham, Edith Cheng, Cassandra Wong, Anne-Claude Gingras, and Grant Brown. The files are associated with a manuscript submitted for publication by Jung Jennifer Ho et al. The main goal of this paper was to profile the proximity interactome of BLM-TOP3A-RMI1-RMI2 (BTRR) complex to identify proteins that suppress recombination in DNA repair. This dataset identifies the importance of RAD54L2 for the recruitment of Bloom (BLM) helicase to promote non-crossover recombination. Grant W. Brown is the corresponding author of the manuscript (grant.brown@utoronto.ca); Anne-Claude Gingras should be contacted for questions on this dataset (gingras@lunenfeld.ca) [doi:10.25345/C5930P58Q] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: BLM ; TOP3A ; RMI1 ; RMI2 ; BioID ; Bloom helicase

Contact

Principal Investigators:
(in alphabetical order) 		Anne-Claude Gingras, LTRI, Canada
Submitting User: gingraslab
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Experimental Design
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Identification Results
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Quantification Results
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Number of distinct conditions across all analyses (original submission and reanalyses) associated with this dataset.

Distinct condition labels are counted across all files submitted in the "Metadata" category having a "Condition" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

Distinct replicate labels are counted across all files submitted in the "Metadata" category having a "BioReplicate" or "Replicate" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct technical replicates across all analyses (original submission and reanalyses) associated with this dataset.

The technical replicate count is defined as the maximum number of times any one distinct combination of condition and biological replicate was analyzed across all files submitted in the "Metadata" category. In the case of fractionated experiments, only the first fraction is considered.

"N/A" means no results of this type were submitted.
Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

"N/A" means no results of this type were submitted.
Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct unmodified peptide sequences reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Total number of peptide-spectrum matches (i.e. spectrum identifications) reported across all analyses (original submission and reanalyses) associated with this dataset.

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

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