[ { "title": "A novel human metalloprotease synthesized in the liver and secreted into the blood: possibly, the von Willebrand factor-cleaving protease?", "journal": "J. Biochem.", "date": "2001", "authors": "Soejima K, Mimura N, Hirashima M, Maeda H, Hamamoto T, Nakagaki T, Nozaki C", "reference": { "type": "PubMed", "id": "11574066", "url": "https://pubmed.ncbi.nlm.nih.gov/11574066" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q76LX8-1", "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 13", "gene_name": "ADAMTS13", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q76LX8", "url": "https://www.uniprot.org/uniprotkb/Q76LX8" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.11574066", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", 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"Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency.", "journal": "Kidney international", "date": "2003", "authors": "Assink K, Schiphorst R, Allford S, Karpman D, Etzioni A, Brichard B, van de Kar N, Monnens L, van den Heuvel L", "reference": { "type": "PubMed", "id": "12753286", "url": "https://pubmed.ncbi.nlm.nih.gov/12753286" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q76LX8-1", "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 13", "gene_name": "ADAMTS13", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q76LX8", "url": "https://www.uniprot.org/uniprotkb/Q76LX8" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.12753286", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], 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Biol. Chem.", "date": "2003", "authors": "Zheng Xinglong, Nishio Kenji, Majerus Elaine M, Sadler J Evan", "reference": { "type": "PubMed", "id": "12791682", "url": "https://pubmed.ncbi.nlm.nih.gov/12791682" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q76LX8-1", "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 13", "gene_name": "ADAMTS13", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q76LX8", "url": "https://www.uniprot.org/uniprotkb/Q76LX8" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.12791682", "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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in association with a mutation in the second CUB domain of ADAMTS13.", "journal": "Blood", "date": "2004", "authors": "Pimanda JE, Maekawa A, Wind T, Paxton J, Chesterman CN, Hogg PJ", "reference": { "type": "PubMed", "id": "14512317", "url": "https://pubmed.ncbi.nlm.nih.gov/14512317" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q76LX8-1", "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 13", "gene_name": "ADAMTS13", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q76LX8", "url": "https://www.uniprot.org/uniprotkb/Q76LX8" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.14512317", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": 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[] } ] }, { "title": "Two novel ADAMTS13 gene mutations in thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome (TTP/HUS).", "journal": "Kidney international", "date": "2004", "authors": "Licht C, Stapenhorst L, Simon T, Budde U, Schneppenheim R, Hoppe B", "reference": { "type": "PubMed", "id": "15327386", "url": "https://pubmed.ncbi.nlm.nih.gov/15327386" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q76LX8-1", "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 13", "gene_name": "ADAMTS13", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q76LX8", "url": "https://www.uniprot.org/uniprotkb/Q76LX8" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.15327386", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], 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Biol. Chem.", "date": "2006", "authors": "Anderson Patricia J, Kokame Koichi, Sadler J Evan", "reference": { "type": "PubMed", "id": "16286459", "url": "https://pubmed.ncbi.nlm.nih.gov/16286459" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q76LX8-1", "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 13", "gene_name": "ADAMTS13", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q76LX8", "url": "https://www.uniprot.org/uniprotkb/Q76LX8" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.16286459", "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", 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"[Identification of two novel mutations in ADAMTS13 gene in a patient with hereditary thrombotic thrombocytopenic purpura].", "journal": "Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi", "date": "2005", "authors": "Liu F, Jin J, Dong NZ, Wang YG, Ruan CG", "reference": { "type": "PubMed", "id": "16468327", "url": "https://pubmed.ncbi.nlm.nih.gov/16468327" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q76LX8-1", "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 13", "gene_name": "ADAMTS13", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q76LX8", "url": "https://www.uniprot.org/uniprotkb/Q76LX8" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.16468327", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], 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[] } ] }, { "title": "Loss of VRK1 alters the nuclear phosphoproteome in the DNA damage response to doxorubicin.", "journal": "Chemico-biological interactions", "date": "2024-03-01", "authors": "Navarro-Carrasco Elena, Campos-D\u00edaz Aurora, Monte-Serrano Eva, Rolfs Frank, de Goeij-de Haas Richard, Pham Thang V, Piersma Sander R, Jim\u00e9nez Connie R, Lazo Pedro A", "reference": { "type": "PubMed", "id": "38367682", "url": "https://pubmed.ncbi.nlm.nih.gov/38367682" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q99986-1", "protein_name": "Serine/threonine-protein kinase VRK1", "gene_name": "VRK1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q99986", "url": "https://www.uniprot.org/uniprotkb/Q99986" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.38367682", "abstract": "", "glycosylation": [], 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pyridoxine 5'-phosphate oxidase.", "journal": "Protein science : a publication of the Protein Society", "date": "2003", "authors": "Musayev FN, Di Salvo ML, Ko TP, Schirch V, Safo MK", "reference": { "type": "PubMed", "id": "12824491", "url": "https://pubmed.ncbi.nlm.nih.gov/12824491" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9NVS9-1", "protein_name": "Pyridoxine-5'-phosphate oxidase", "gene_name": "PNPO", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q9NVS9", "url": "https://www.uniprot.org/uniprotkb/Q9NVS9" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.12824491", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": 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"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": "Characterization of Novel Pathogenic Variants Causing Pyridox(am)ine 5'-Phosphate Oxidase-Dependent Epilepsy.", 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