<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Ting Dong</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018855000</full_dataset_link><submitter_email>tingdong2025@pumc.edu.cn</submitter_email><submitter_affiliation>Institute of Medicinal Biotechnology (IMB), Chinese Academy of Medical Sciences &amp;amp; Peking Union Medical College</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Identification of FAK-interacting proteins by LC-MS/MS from silver-stained gel bands</name><description>FAK (focal adhesion kinase) is a key regulator of cell adhesion and signaling. To identify potential FAK-interacting proteins, we expressed FLAG-tagged FAK (FAK-FLAG) or empty vector (EV) control in HEK293T cells, followed by anti-FLAG affinity pull-down. The immunoprecipitated complexes were resolved by SDS-PAGE and visualized by silver staining. Specific protein bands enriched in the FAK-FLAG lane compared to the EV control were excised, subjected to in‑gel trypsin digestion, and analyzed by LC‑MS/MS. Protein identification was performed, revealing their potential association with FAK. This dataset provides the raw mass spectrometry data and identification results for these candidate interactors.</description><dates><publication>Thu Aug 06 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD082260</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>