MassIVE MSV000098505

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GNPS-coniotin high-resolution mass spectrometry data

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Description

We purified coniotin from Coniochaeta fungus and determined its high-resolution mass (MS and MS/MS) using an Agilent 1290 Infinity II HPLC system coupled to a 6550 Q-TOF ESI/MS. Here, we deposit the full high-resolution electrospray ionization mass spectrometry data of coniotin to GNPS for public access and reference. [doi:10.25345/C5057D541] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Coniotin ; high-resolution mass ; MS/MS ; Papain hydrolysis ; Marfey ; DatasetType:Other (Coniotin high-resolution electrospray ionization mass spectrometry data)

Contact

Principal Investigators:
(in alphabetical order) 		Kalinka Koteva, McMaster University, Canada
Xuefei Chen, McMaster University, Canada
Submitting User: Xuefei731

Publications

Chen X, Koteva K, Chou S, Guitor A, Pallant D, Lee Y, Sychantha D, French S, Hackenberger D, Robbins N, Cook MA, Brown ED, MacNeil LT, Cowen LE, Wright GD.
Coniontins, lipopetaibiotics active against Candida auris identified from a microbial natural product fractionation library.
Nat Commun. 2025 Aug 8;16(1):7337. Epub 2025 Aug 8.

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GNPS content goes here (MSV000098505 [task=dc4db1110cd8407ab6e3e3db94e01dbf])
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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.

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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.

"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.