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Peptide mixtures (200 ng per injection) were separated using a nanoElute UHPLC system (Bruker Daltonics) coupled to a timsTOF Pro 2 mass spectrometer equipped with a CaptiveSpray nanoelectrospray source.  Peptides were loaded onto a Bruker FIFTEEN C18 column (15 cm × 75 μm ID, 1.9 μm particle size) and separated at 30 °C using a 20-min gradient at 300 nL min⁻¹ (mobile phase A: 0.1% formic acid; mobile phase B: 0.1% formic acid in acetonitrile).  The elution gradient was 0–35% B for 13 min, 35–90% B from 13–15 min, followed by a wash at 90% B.  Mass spectrometry acquisition was performed on a timsTOF Pro 2 in data-dependent acquisition mode using the PASEF method, acquiring MS and MS/MS spectra in the m/z range 100–1700. Ion mobility separation ranged from 0.85 to 1.30 V·s cm⁻² with a ramp time of 100 ms.  Four PASEF MS/MS scans were acquired per cycle. Active exclusion was set to 0.4 min for precursors above 20,000 intensity units.</sample_protocol><repository>Pride</repository><quantification_method></quantification_method><modification></modification><data_protocol>Raw LC–TIMS–MS/MS data were processed using PEAKS Studio ProX (Bioinformatics Solutions Inc.).  MS/MS spectra were searched against a combined UniProt database containing the reference proteomes of the analysed yeast strains and Botrytis cinerea.  Search parameters included a precursor mass tolerance of 15 ppm and fragment tolerance of 0.05 Da, with carbamidomethylation of cysteine as fixed modification and methionine oxidation and N-terminal acetylation as variable modifications.  Protein identifications were validated using a target–decoy strategy with a false discovery rate (FDR) threshold of 1%.  Proteins supported by at least two unique peptides and −10lgP ≥ 25 were retained for downstream analysis.  Protein intensities were log2-transformed, normalized by median centering, and missing values were imputed using a minimum-intensity approach.  Differential abundance analysis was performed using empirical Bayes linear modelling implemented in the limma package in R (v4.3.2), applying Benjamini–Hochberg correction and considering proteins with FDR ≤ 0.05 and |log2FC| ≥ 0.58 as differentially abundant.</data_protocol><omics_type>Proteomics</omics_type><labhead>Jose Luis Padilla Agudelo</labhead><instrument_platform></instrument_platform><labhead_affiliation>Department of Biomedicine, Biotechnology and Public Health, University of Cádiz, Spain</labhead_affiliation><submission_type>PARTIAL</submission_type><species>Pichia Kluyveri</species><species>Pichia Kudriavzevii</species><submitter_mail>joseluis.padilla@uca.es</submitter_mail><publication>10.1016/J.FM.2026.105112</publication><submitter_affiliation>University of Cádiz</submitter_affiliation><submitter_country>Spain</submitter_country></additional><is_claimable>false</is_claimable><name>Distinct physiological strategies underpin antagonism of native Pichia yeasts against Botrytis cinerea</name><description>Proteomics dataset generated using LC-MS/MS on a Bruker timsTOF instrument with DDA-PASEF acquisition. Protein identification was performed using PEAKS software. The dataset includes raw instrument files (.d folders) and processed peptide and protein identification results.</description><dates><publication>2026-04-21</publication><submission>2026-03-07</submission></dates><accession>PXD075355</accession><cross_references><TAXONOMY>NEWT:6945</TAXONOMY><TAXONOMY>NEWT:3555</TAXONOMY><TAXONOMY>NEWT:2</TAXONOMY><TAXONOMY>NEWT:157546</TAXONOMY><TAXONOMY>NEWT:35554</TAXONOMY><TAXONOMY>NEWT:38942</TAXONOMY><TAXONOMY>NEWT:307972</TAXONOMY><TAXONOMY>NEWT:32046</TAXONOMY><TAXONOMY>NEWT:544496</TAXONOMY><TAXONOMY>NEWT:2042546</TAXONOMY><TAXONOMY>NEWT:45351</TAXONOMY><TAXONOMY>NEWT:43179</TAXONOMY><TAXONOMY>NEWT:4513</TAXONOMY><TAXONOMY>NEWT:5722</TAXONOMY><TAXONOMY>NEWT:55153</TAXONOMY><TAXONOMY>NCBITaxon:10407</TAXONOMY><TAXONOMY>NEWT:1736309</TAXONOMY><TAXONOMY>NEWT:309800</TAXONOMY><TAXONOMY>NEWT:1211601</TAXONOMY><TAXONOMY>NEWT:876138</TAXONOMY><TAXONOMY>NEWT:237561</TAXONOMY><TAXONOMY>NEWT:5833</TAXONOMY><TAXONOMY>NEWT:6928</TAXONOMY><TAXONOMY>NEWT:10036</TAXONOMY><TAXONOMY>NEWT:36745</TAXONOMY><TAXONOMY>NEWT:1351</TAXONOMY><TAXONOMY>NEWT:1438992</TAXONOMY><TAXONOMY>NEWT:2649997</TAXONOMY><TAXONOMY>NEWT:272563</TAXONOMY><TAXONOMY>NEWT:224326</TAXONOMY><TAXONOMY>NCBITaxon:79857</TAXONOMY><TAXONOMY>NEWT:1096976</TAXONOMY><TAXONOMY>NEWT:95648</TAXONOMY><TAXONOMY>NEWT:3885</TAXONOMY><TAXONOMY>NEWT:3888</TAXONOMY><TAXONOMY>NEWT:1589</TAXONOMY><TAXONOMY>NEWT:135622</TAXONOMY><TAXONOMY>NEWT:6915</TAXONOMY><TAXONOMY>NEWT:3649</TAXONOMY><TAXONOMY>NEWT:101510</TAXONOMY><TAXONOMY>NEWT:3880</TAXONOMY><TAXONOMY>NEWT:272559</TAXONOMY><TAXONOMY>NEWT:3641</TAXONOMY><TAXONOMY>NEWT:383379</TAXONOMY><TAXONOMY>NEWT:466585</TAXONOMY><TAXONOMY>NEWT:10029</TAXONOMY><TAXONOMY>NEWT:1000589</TAXONOMY><TAXONOMY>NEWT:85963</TAXONOMY><TAXONOMY>NEWT:85962</TAXONOMY><TAXONOMY>NEWT:317447</TAXONOMY><TAXONOMY>NEWT:7955</TAXONOMY><TAXONOMY>NEWT:7959</TAXONOMY><TAXONOMY>NEWT:2261</TAXONOMY><TAXONOMY>NEWT:31156</TAXONOMY><TAXONOMY>NEWT:398580</TAXONOMY><TAXONOMY>NEWT:4565</TAXONOMY><TAXONOMY>NEWT:1264690</TAXONOMY><TAXONOMY>NEWT:515619</TAXONOMY><TAXONOMY>NEWT:192875</TAXONOMY><TAXONOMY>NEWT:34305</TAXONOMY><TAXONOMY>NEWT:59729</TAXONOMY><TAXONOMY>NCBITaxon:183674</TAXONOMY><TAXONOMY>NEWT:224308</TAXONOMY><TAXONOMY>NEWT:84645</TAXONOMY><TAXONOMY>NEWT:626528</TAXONOMY><TAXONOMY>NEWT:139927</TAXONOMY><TAXONOMY>NEWT:4558</TAXONOMY><TAXONOMY>NEWT:209285</TAXONOMY><TAXONOMY>NEWT:1283</TAXONOMY><TAXONOMY>NEWT:931281</TAXONOMY><TAXONOMY>NEWT:4550</TAXONOMY><TAXONOMY>NEWT:1000561</TAXONOMY><TAXONOMY>NEWT:197</TAXONOMY><TAXONOMY>NCBITaxon:79824</TAXONOMY><TAXONOMY>NEWT:4787</TAXONOMY><TAXONOMY>NCBITaxon:4563</TAXONOMY><TAXONOMY>NEWT:5755</TAXONOMY><TAXONOMY>NEWT:44689</TAXONOMY><TAXONOMY>NEWT:3218</TAXONOMY><TAXONOMY>NEWT:5759</TAXONOMY><TAXONOMY>NEWT:1736231</TAXONOMY><TAXONOMY>NEWT:1270</TAXONOMY><TAXONOMY>NEWT:2242</TAXONOMY><TAXONOMY>NEWT:4784</TAXONOMY><TAXONOMY>NEWT:11320</TAXONOMY><TAXONOMY>NEWT:360106</TAXONOMY><TAXONOMY>NEWT:286</TAXONOMY><TAXONOMY>NEWT:287</TAXONOMY><TAXONOMY>NEWT:10117</TAXONOMY><TAXONOMY>NEWT:10239</TAXONOMY><TAXONOMY>NEWT:10116</TAXONOMY><TAXONOMY>NEWT:1280</TAXONOMY><TAXONOMY>NEWT:1735272</TAXONOMY><TAXONOMY>NEWT:83334</TAXONOMY><TAXONOMY>NEWT:83332</TAXONOMY><TAXONOMY>NEWT:44685</TAXONOMY><TAXONOMY>NEWT:317513</TAXONOMY><TAXONOMY>NEWT:1148</TAXONOMY><TAXONOMY>NEWT:580240</TAXONOMY><TAXONOMY>NEWT:294128</TAXONOMY><TAXONOMY>NEWT:11676</TAXONOMY><TAXONOMY>NEWT:55571</TAXONOMY><TAXONOMY>NEWT:100226</TAXONOMY><TAXONOMY>NEWT:4530</TAXONOMY><TAXONOMY>NEWT:4896</TAXONOMY><TAXONOMY>NEWT:75058</TAXONOMY><TAXONOMY>NEWT:13616</TAXONOMY><TAXONOMY>NEWT:1094343</TAXONOMY><TAXONOMY>NEWT:296543</TAXONOMY><TAXONOMY>NEWT:1773</TAXONOMY><TAXONOMY>NEWT:1895</TAXONOMY><TAXONOMY>NEWT:1182590</TAXONOMY><TAXONOMY>NEWT:3712</TAXONOMY><TAXONOMY>NEWT:935293</TAXONOMY><TAXONOMY>NEWT:64152</TAXONOMY><TAXONOMY>NEWT:4924</TAXONOMY><TAXONOMY>NEWT:749200</TAXONOMY><TAXONOMY>NEWT:990346</TAXONOMY><TAXONOMY>NEWT:145953</TAXONOMY><TAXONOMY>NEWT:257309</TAXONOMY><TAXONOMY>NEWT:100816</TAXONOMY><TAXONOMY>NEWT:263</TAXONOMY><TAXONOMY>NEWT:230741</TAXONOMY><TAXONOMY>NEWT:52283</TAXONOMY><TAXONOMY>NEWT:284812</TAXONOMY><TAXONOMY>NCBITaxon:1313</TAXONOMY><TAXONOMY>NEWT:43330</TAXONOMY><TAXONOMY>NEWT:1603293</TAXONOMY><TAXONOMY>NEWT:408169</TAXONOMY><TAXONOMY>NEWT:44544</TAXONOMY><TAXONOMY>NEWT:4911</TAXONOMY><TAXONOMY>NEWT:645463</TAXONOMY><TAXONOMY>NEWT:3702</TAXONOMY><TAXONOMY>NEWT:129249</TAXONOMY><TAXONOMY>NEWT:243277</TAXONOMY><TAXONOMY>NEWT:990119</TAXONOMY><TAXONOMY>NEWT:408172</TAXONOMY><TAXONOMY>NEWT:408170</TAXONOMY><TAXONOMY>NEWT:493760</TAXONOMY><TAXONOMY>NEWT:260710</TAXONOMY><TAXONOMY>NEWT:257313</TAXONOMY><TAXONOMY>NEWT:400772</TAXONOMY><TAXONOMY>NEWT:3708</TAXONOMY><TAXONOMY>NEWT:128161</TAXONOMY><TAXONOMY>NEWT:332648</TAXONOMY><TAXONOMY>NEWT:106592</TAXONOMY><TAXONOMY>NEWT:536231</TAXONOMY><TAXONOMY>NEWT:460519</TAXONOMY><TAXONOMY>NEWT:1187947</TAXONOMY><TAXONOMY>NEWT:1432138</TAXONOMY><TAXONOMY>NEWT:10312</TAXONOMY><TAXONOMY>NEWT:1424507</TAXONOMY><TAXONOMY>NCBITaxon:1773</TAXONOMY><TAXONOMY>NEWT:9598</TAXONOMY>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ashMap>