MassIVE MSV000097665

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GNPS - Bile Salt Hydrolase Screening with bile acid and amines

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Description

120 Bile Salt Hydrolases (BSH) and Penicillin V Acylase (PVA) enzymes from various microbial strains were overexpressed in E. coli and purified using nickel affinity chromatography. Enzyme assays were performed by incubating the purified enzymes with 18 bile acids and 49 amines. Following incubation, the reactions were quenched, and the extracts were dried and reconstituted in 80% methanol containing an internal standard. MS/MS data acquisition was carried out on Thermo Exploris 240 mass spectrometer in positive ionization mode, with chromatographic separation achieved using a Phenomenex Polar C18 column. [doi:10.25345/C5RX93R9H] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: BSH ; Bile Salt Hydrolase ; DatasetType:Metabolomics

Contact

Principal Investigators:
(in alphabetical order) 		Pieter C. Dorrestein, University of California at San Diego, USA
Submitting User: Dpattynama1
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Identification Results
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GNPS content goes here (MSV000097665 [task=befd985715e7403992760fda4973a68b])
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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.

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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.

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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.

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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 unmodified peptide sequences 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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Total number of peptide-spectrum matches (i.e. spectrum identifications) 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.

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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.