{"database":"MassIVE","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://massive-ftp.ucsd.edu/v09/MSV000096929/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"submitter":["Keiko Torii"],"full_dataset_link":["https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=8260c88950e04426b2d1f4a24aaae7d1"],"submitter_email":["ktorii@utexas.edu"],"sample_protocol":[""],"repository":["MassIVE"],"file_size":["108"],"ptm_modification":["MS:1002864 - No post-translational-modifications are included in the identified peptides of this dataset"],"data_protocol":[""],"omics_type":["Proteomics"],"instrument_platform":["Orbitrap Fusion Lumos"],"species":["Arabidopsis Thaliana (ncbitaxon:3702)"],"submitter_affiliation":["University of Texas at Austin"],"additional_accession":["PXD060161"]},"is_claimable":false,"name":"Comparative Proteomic Profiling of Receptor Kinase Signaling Reveals Key Trafficking Components Enforcing Plant Stomatal Development","description":"This entry contains 45 raw files from proteomic experiments involving TurboID-based proximity labeling (TurboID-PL, 9 samples with 2 injection replicates each, totaling 18 raw files) and HA-tagged affinity purification mass spectrometry (HA-AP, 9 samples with 3 injection replicates each, totaling 27 raw files). Arabidopsis tissues were used for both TurboID-PL and HA-AP. The ERECTA-TurboID (E) sample group served as the experimental group, with Lit6B-TurboID (L) and er-105 mutant (m) serving as negative controls. All samples were digested with trypsin, and LC-MS/MS analysis was performed by Dr. Marcotte lab to identify ERECTA-associated protein complexes.","dates":{"publication":"Fri Jan 24 07:44:00 GMT 2025"},"accession":"MSV000096929","cross_references":{}}