MassIVE MSV000093675

Partial Public

TcSERPIN_an_inhibitor_that interacts_with_cocoa_defense_proteins_and_has_biotechnological_potential_against_human_pathogens

Description

The objective of this study was to characterize a serpin from Theobroma cacao, called TcSERPIN, to identify its endogenous targets and determine its function and biotechnological potential. The protease trap containing immobilized rTcSERPIN captured endogenous defense proteins from cocoa extracts that are related to metabolic pathways, stress and defense. [doi:10.25345/C5862BP0X] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Serpin ; Theobroma cacao ; Protease inhibitor

Contact

Principal Investigators:
(in alphabetical order)
Akyla Maria Martins Alves, Universidade Estadual de Santa Cruz (UESC), Brazil
Andria dos Santos Freitas, Universidade Estadual de Santa Cruz (UESC), Brazil
Ariana Silva Santos, Universidade Estadual de Santa Cruz (UESC), Brazil
Brenda Concei��o Guimar�es Santana, Universidade Estadual de Santa Cruz (UESC), Brazil
Bruno Silva Andrade, Universidade Estadual de Santa Cruz (UESC), Brazil
Carlos Priminho Pirovani, State University of Santa Cruz, Brazil
Geiseane Velozo Amaral geiseanevelozo@gmail.com, Universidade Estadual de Santa Cruz (UESC), Brazil
Irma Yuliana Mora-Ocampo, State University of Santa Cruz, Brazil
Keilane Silva Farias, Universidade Estadual de Santa Cruz (UESC), Brazil
Maria Lu�za do Carmo Santos, Universidade Estadual de Santa Cruz (UESC), Brazil
Maria Zugaib, Universidade Estadual de Santa Cruz (UESC), Brazil, Brazil
Monaliza Macedo Ferreira, Universidade Estadual de Santa Cruz (UESC), Brazil
Submitting User: yulimora
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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.

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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.

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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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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.