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Commun.", "date": "2008", "authors": "Kato H, Mihara K", "reference": { "type": "PubMed", "id": "18331822", "url": "https://pubmed.ncbi.nlm.nih.gov/18331822" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q8N4H5-1", "protein_name": "Mitochondrial import receptor subunit TOM5 homolog", "gene_name": "TOMM5", "tax_name": "Human" }, { "uniprot_canonical_ac": "Q15388-1", "protein_name": "Mitochondrial import receptor subunit TOM20 homolog", "gene_name": "TOMM20", "tax_name": "Human" }, { "uniprot_canonical_ac": "Q9P0U1-1", "protein_name": "Mitochondrial import receptor subunit TOM7 homolog", "gene_name": "TOMM7", "tax_name": "Human" }, { "uniprot_canonical_ac": "O96008-1", "protein_name": "Mitochondrial import receptor subunit TOM40 homolog", "gene_name": "TOMM40", "tax_name": "Human" }, { "uniprot_canonical_ac": "Q9NS69-1", "protein_name": "Mitochondrial import receptor subunit TOM22 homolog", "gene_name": "TOMM22", "tax_name": "Human" }, { "uniprot_canonical_ac": "Q96B49-1", "protein_name": "Mitochondrial import receptor subunit TOM6 homolog", "gene_name": "TOMM6", "tax_name": "Human" }, { "uniprot_canonical_ac": "O94826-1", "protein_name": "Mitochondrial import receptor subunit TOM70", "gene_name": "TOMM70", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q8N4H5", "url": "https://www.uniprot.org/uniprotkb/Q8N4H5" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.18331822", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 7 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": "referenced_glycans", "table_stats": [ { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation", "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": "phosphorylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_reported", "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_reported_with_glycan", "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_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": "Solution structure and dynamics of Ufm1, a ubiquitin-fold modifier 1.", "journal": "Biochem. Biophys. Res. Commun.", "date": "2006", "authors": "Sasakawa H, Sakata E, Yamaguchi Y, Komatsu M, Tatsumi K, Kominami E, Tanaka K, Kato K", "reference": { "type": "PubMed", "id": "16527251", "url": "https://pubmed.ncbi.nlm.nih.gov/16527251" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P61960-1", "protein_name": "Ubiquitin-fold modifier 1", "gene_name": "UFM1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P61960", "url": "https://www.uniprot.org/uniprotkb/P61960" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.16527251", "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" 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"count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "Human UFSP1 translated from an upstream near-cognate initiation codon functions as an active UFM1-specific protease.", "journal": "The Journal of biological chemistry", "date": "2022", "authors": "Liang Q, Jin Y, Xu S, Zhou J, Mao J, Ma X, Wang M, Cong YS", "reference": { "type": "PubMed", "id": "35525273", "url": "https://pubmed.ncbi.nlm.nih.gov/35525273" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P61960-1", "protein_name": "Ubiquitin-fold modifier 1", "gene_name": "UFM1", "tax_name": "Human" }, { "uniprot_canonical_ac": "Q6NVU6-1", "protein_name": "Ufm1-specific protease 1", "gene_name": "UFSP1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P61960", "url": "https://www.uniprot.org/uniprotkb/P61960" } ], "common_name": 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"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": "Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.", "journal": "Nature genetics", "date": "2010", "authors": "Deng HX, Klein CJ, Yan J, Shi Y, Wu Y, Fecto F, Yau HJ, Yang Y, Zhai H, Siddique N, Hedley-Whyte ET, Delong R, Martina M, Dyck PJ, Siddique T", "reference": { "type": "PubMed", "id": "20037587", "url": "https://pubmed.ncbi.nlm.nih.gov/20037587" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9HBA0-1", "protein_name": "Transient receptor potential 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"count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C.", "journal": "Nature genetics", "date": "2010", "authors": "Auer-Grumbach M, Olschewski A, Papic L, Kremer H, McEntagart ME, Uhrig S, Fischer C, Frohlich E, Balint Z, Tang B, Strohmaier H, Lochmuller H, Schlotter-Weigel B, Senderek J, Krebs A, Dick KJ, Petty R, Longman C, Anderson NE, Padberg GW, Schelhaas HJ, van Ravenswaaij-Arts CM, Pieber TR, Crosby AH, Guelly C", "reference": { "type": "PubMed", "id": "20037588", "url": "https://pubmed.ncbi.nlm.nih.gov/20037588" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9HBA0-1", "protein_name": "Transient receptor potential cation channel subfamily V member 4", "gene_name": "TRPV4", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, 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"Dominant TRPV4 mutations in nonlethal and lethal metatropic dysplasia.", "journal": "American journal of medical genetics. Part A", "date": "2010", "authors": "Camacho N, Krakow D, Johnykutty S, Katzman PJ, Pepkowitz S, Vriens J, Nilius B, Boyce BF, Cohn DH", "reference": { "type": "PubMed", "id": "20425821", "url": "https://pubmed.ncbi.nlm.nih.gov/20425821" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9HBA0-1", "protein_name": "Transient receptor potential cation channel subfamily V member 4", "gene_name": "TRPV4", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q9HBA0", "url": "https://www.uniprot.org/uniprotkb/Q9HBA0" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.20425821", "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": "referenced_glycans", "table_stats": [ { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation", "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": "phosphorylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_reported", "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_reported_with_glycan", "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_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": "Spondylo-epiphyseal dysplasia, Maroteaux type (pseudo-Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations.", "journal": "American journal of medical genetics. Part A", "date": "2010", "authors": "Nishimura G, Dai J, Lausch E, Unger S, Megarbane A, Kitoh H, Kim OH, Cho TJ, Bedeschi F, Benedicenti F, Mendoza-Londono R, Silengo M, Schmidt-Rimpler M, Spranger J, Zabel B, Ikegawa S, Superti-Furga A", "reference": { "type": "PubMed", "id": "20503319", "url": "https://pubmed.ncbi.nlm.nih.gov/20503319" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9HBA0-1", "protein_name": "Transient receptor potential cation channel subfamily V member 4", "gene_name": "TRPV4", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q9HBA0", "url": "https://www.uniprot.org/uniprotkb/Q9HBA0" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.20503319", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": 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Biol. 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"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": "The human UDP-glucuronosyltransferase UGT1A3 is highly selective towards N2 in the tetrazole ring of losartan, candesartan, and zolarsartan.", "journal": "Biochemical pharmacology", "date": "2008-09-15", "authors": "Alonen Anna, Finel Moshe, Kostiainen Risto", "reference": { "type": "PubMed", "id": "18674515", "url": "https://pubmed.ncbi.nlm.nih.gov/18674515" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9HAW7-1", "protein_name": "UDP-glucuronosyltransferase 1A7", "gene_name": "UGT1A7", "tax_name": "Human" 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[] } ] }, { "title": "Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy.", "journal": "Genetics in medicine : official journal of the American College of Medical Genetics", "date": "2024-06", "authors": "Zeitz Christina, Navarro Julien, Azizzadeh Pormehr Leila, M\u00e9j\u00e9case C\u00e9cile, Neves Luiza M, Letellier Camille, Condroyer Christel, Albadri Shahad, Amprou Andr\u00e9a, Antonio Aline, Ben-Yacoub Tasnim, Wohlschlegel Juliette, Andrieu Camille, Serafini Malo, Bianco Lorenzo, Antropoli Alessio, Nassisi Marco, El Shamieh Said, Chantot-Bastaraud Sandra, Mohand-Sa\u00efd Saddek, Smirnov Vasily, Sahel Jos\u00e9-Alain, Del Bene Filippo, Audo Isabelle", "reference": { "type": "PubMed", "id": "38293907", "url": "https://pubmed.ncbi.nlm.nih.gov/38293907" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "F5GYI3-1", "protein_name": "Ubiquitin-associated protein 1-like", "gene_name": "UBAP1L", "tax_name": "Human" } ], "species": 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