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A, Koga Y, Suzuki H, Uehara T, Kosaki K, Yoshiura KI, Mishima H, Ichimiya Y, Mushimoto Y, Horinouchi T, Nagano C, Yamamura T, Iijima K, Nozu K", "reference": { "type": "PubMed", "id": "34650211", "url": "https://pubmed.ncbi.nlm.nih.gov/34650211" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9Y276-1", "protein_name": "Mitochondrial chaperone BCS1", "gene_name": "BCS1L", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q9Y276", "url": "https://www.uniprot.org/uniprotkb/Q9Y276" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.34650211", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", 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[] } ] }, { "title": "Nonstructural 5A Protein of Hepatitis C Virus Regulates Soluble Resistance-Related Calcium-Binding Protein Activity for Viral Propagation.", "journal": "Journal of virology", "date": "2015", "authors": "Tran GV, Luong TT, Park EM, Kim JW, Choi JW, Park C, Lim YS, Hwang SB", "reference": { "type": "PubMed", "id": "26719254", "url": "https://pubmed.ncbi.nlm.nih.gov/26719254" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P30626-1", "protein_name": "Sorcin", "gene_name": "SRI", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P30626", "url": "https://www.uniprot.org/uniprotkb/P30626" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "phosphorylation": [ { "start_pos": 155, "end_pos": 155, "kinase_uniprot_canonical_ac": "", "kinase_gene_name": "", "residue": "Thr", "comment": "", "evidence": [ { "database": 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"field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_predicted", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "Sorcin is an early marker of neurodegeneration, Ca(2+) dysregulation and endoplasmic reticulum stress associated to neurodegenerative diseases.", "journal": "Cell death & disease", "date": "2020", "authors": "Genovese I, Giamogante F, Barazzuol L, Battista T, Fiorillo A, Vicario M, D'Alessandro G, Cipriani R, Limatola C, Rossi D, Sorrentino V, Poser E, Mosca L, Squitieri F, Perluigi M, Arena A, van Petegem F, Tito C, Fazi F, Giorgi C, Cali T, Ilari A, Colotti G", "reference": { "type": "PubMed", "id": "33060591", "url": "https://pubmed.ncbi.nlm.nih.gov/33060591" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P30626-1", "protein_name": "Sorcin", "gene_name": "SRI", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": 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transcriptional activity of the unfolded protein response mediator ATF6.", "journal": "FEBS letters", "date": "2021", "authors": "Parks SZ, Gao T, Jimenez Awuapura N, Ayathamattam J, Chabosseau PL, Kalvakolanu DV, Valdivia HH, Rutter GA, Leclerc I", "reference": { "type": "PubMed", "id": "33960419", "url": "https://pubmed.ncbi.nlm.nih.gov/33960419" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P30626-1", "protein_name": "Sorcin", "gene_name": "SRI", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P30626", "url": "https://www.uniprot.org/uniprotkb/P30626" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.33960419", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": 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member of the kinectin and ES/130 family, maps to human chromosome band 14q22.", "journal": "Immunogenetics", "date": "1996", "authors": "Print CG, Morris CM, Spurr NK, Rooke L, Krissansen GW", "reference": { "type": "PubMed", "id": "8575822", "url": "https://pubmed.ncbi.nlm.nih.gov/8575822" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q86UP2-1", "protein_name": "Kinectin", "gene_name": "KTN1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q86UP2", "url": "https://www.uniprot.org/uniprotkb/Q86UP2" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.8575822", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ 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loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.", "journal": "American journal of ophthalmology", "date": "2004", "authors": "Payne M, Yang Z, Katz BJ, Warner JE, Weight CJ, Zhao Y, Pearson ED, Treft RL, Hillman T, Kennedy RJ, Meire FM, Zhang K", "reference": { "type": "PubMed", "id": "15531309", "url": "https://pubmed.ncbi.nlm.nih.gov/15531309" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "O60313-1", "protein_name": "Dynamin-like GTPase OPA1, mitochondrial", "gene_name": "OPA1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "O60313", "url": "https://www.uniprot.org/uniprotkb/O60313" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.15531309", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": 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Boissiere A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K, Letournel F, Liguori R, La Morgia C, Montagna P, Liguori M, Zanna C, Rugolo M, Cossarizza A, Wissinger B, Verny C, Schwarzenbacher R, Martin MA, Arenas J, Ayuso C, Garesse R, Lenaers G, Bonneau D, Carelli V", "reference": { "type": "PubMed", "id": "18158317", "url": "https://pubmed.ncbi.nlm.nih.gov/18158317" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "O60313-1", "protein_name": "Dynamin-like GTPase OPA1, mitochondrial", "gene_name": "OPA1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "O60313", "url": "https://www.uniprot.org/uniprotkb/O60313" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.18158317", "abstract": "", "glycosylation": [], "mutagenesis": [], 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[] } ] }, { "title": "Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.", "journal": "Human mutation", "date": "2009", "authors": "Ferre M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P, Amati-Bonneau P", "reference": { "type": "PubMed", "id": "19319978", "url": "https://pubmed.ncbi.nlm.nih.gov/19319978" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "O60313-1", "protein_name": "Dynamin-like GTPase OPA1, mitochondrial", "gene_name": "OPA1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "O60313", "url": "https://www.uniprot.org/uniprotkb/O60313" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.19319978", "abstract": "", 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Toutain A, Bonneau D, Procaccio V, Amati-Bonneau P, Pisella PJ, Reynier P", "reference": { "type": "PubMed", "id": "19325939", "url": "https://pubmed.ncbi.nlm.nih.gov/19325939" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "O60313-1", "protein_name": "Dynamin-like GTPase OPA1, mitochondrial", "gene_name": "OPA1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "O60313", "url": "https://www.uniprot.org/uniprotkb/O60313" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.19325939", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": 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