{ "bcoid": "GLY_000560", "title": "Human Proteoform Glycosylation Citations (UniProtKB)", "description": "", "filename": "human_proteoform_citations_glycosylation_uniprotkb.csv", "filetype": "csv", "categories": { "species": "Homo sapiens", "molecule": "Proteoform", "tags": "Protein Citations UniProtKB", "file_type": "csv", "status": "Reviewed", "scope": "internal" }, "minitable": { "content": [ [ "P04921-1...", "..." ], [ "Q15910-1...", "..." ] ], "headers": [ "uniprotkb_ca...", "glytoucan_ac..." ], "colwidth": [ "40%", "20%" ] }, "sampledata": { "type": "table", "data": [ [ { "type": "string", "label": "uniprotkb_canonical_ac" }, { "type": "string", "label": "glytoucan_ac" }, { "type": "string", "label": "title" }, { "type": "string", "label": "journal_name" }, { "type": "string", "label": "publication_date" }, { "type": "string", "label": "authors" }, { "type": "string", "label": "xref_key" }, { "type": "string", "label": "xref_id" }, { "type": "string", "label": "src_xref_key" }, { "type": "string", "label": "src_xref_id" } ], [ "P04921-1", "", "N-terminal amino acid sequence of sialoglycoprotein D (glycophorin C) from human erythrocyte membranes.", "European journal of biochemistry", "1982 Jun 15", "Dahr W, Beyreuther K, Kordowicz M, Kruger J", "protein_xref_pubmed", "7106126", "protein_xref_uniprotkb_gly", "P04921" ], [ "Q15910-1", "", "O-GlcNAcylation regulates EZH2 protein stability and function.", "Proceedings of the National Academy of Sciences of the United States of America", "2014 Jan 28", "Chu CS, Lo PW, Yeh YH, Hsu PH, Peng SH, Teng YC, Kang ML, Wong CH, Juan LJ", "protein_xref_pubmed", "24474760", "protein_xref_uniprotkb_gly", "Q15910" ], [ "Q5T6X5-1", "", "N-glycosylation and disulfide bonding affects GPRC6A receptor expression, function, and dimerization.", "FEBS letters", "2015 Feb 27", "Norskov-Lauritsen L, Jorgensen S, Brauner-Osborne H", "protein_xref_pubmed", "25617829", "protein_xref_uniprotkb_gly", "Q5T6X5" ], [ "Q13740-1", "", "Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.", "Journal of proteome research", "2009 Feb", "Chen R, Jiang X, Sun D, Han G, Wang F, Ye M, Wang L, Zou H", "protein_xref_pubmed", "19159218", "protein_xref_uniprotkb_gly", "Q13740" ], [ "Q13740-1", "", "Identification and quantification of N-linked glycoproteins using hydrazide chemistry, stable isotope labeling and mass spectrometry.", "Nature biotechnology", "2003 Jun", "Zhang H, Li XJ, Martin DB, Aebersold R", "protein_xref_pubmed", "12754519", "protein_xref_uniprotkb_gly", "Q13740" ], [ "P35442-1", "", "Structure of the calcium-rich signature domain of human thrombospondin-2.", "Nature structural & molecular biology", "2005 Oct", "Carlson CB, Bernstein DA, Annis DS, Misenheimer TM, Hannah BL, Mosher DF, Keck JL", "protein_xref_pubmed", "16186819", "protein_xref_uniprotkb_gly", "P35442" ], [ "O00469-1", "", "Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.", "Journal of proteome research", "2009 Feb", "Chen R, Jiang X, Sun D, Han G, Wang F, Ye M, Wang L, Zou H", "protein_xref_pubmed", "19159218", "protein_xref_uniprotkb_gly", "O00469" ], [ "P29622-1", "", "Identification and quantification of N-linked glycoproteins using hydrazide chemistry, stable isotope labeling and mass spectrometry.", "Nature biotechnology", "2003 Jun", "Zhang H, Li XJ, Martin DB, Aebersold R", "protein_xref_pubmed", "12754519", "protein_xref_uniprotkb_gly", "P29622" ], [ "P29622-1", "", "Human plasma N-glycoproteome analysis by immunoaffinity subtraction, hydrazide chemistry, and mass spectrometry.", "Journal of proteome research", "2005 Nov-Dec", "Liu T, Qian WJ, Gritsenko MA, Camp DG 2nd, Monroe ME, Moore RJ, Smith RD", "protein_xref_pubmed", "16335952", "protein_xref_uniprotkb_gly", "P29622" ], [ "P01266-1", "", "The structure of human thyroglobulin.", "Nature", "2020 Feb", "Coscia F, Taler-Vercic A, Chang VT, Sinn L, O'Reilly FJ, Izore T, Renko M, Berger I, Rappsilber J, Turk D, Lowe J", "protein_xref_pubmed", "32025030", "protein_xref_uniprotkb_gly", "P01266" ], [ "P06133-1", "", "Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.", "Journal of proteome research", "2009 Feb", "Chen R, Jiang X, Sun D, Han G, Wang F, Ye M, Wang L, Zou H", "protein_xref_pubmed", "19159218", "protein_xref_uniprotkb_gly", "P06133" ], [ "Q96DR5-1", "", "Identification of N-linked glycoproteins in human saliva by glycoprotein capture and mass spectrometry.", "Journal of proteome research", "2006 Jun", "Ramachandran P, Boontheung P, Xie Y, Sondej M, Wong DT, Loo JA", "protein_xref_pubmed", "16740002", "protein_xref_uniprotkb_gly", "Q96DR5" ], [ "Q14126-1", "", "Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.", "Journal of proteome research", "2009 Feb", "Chen R, Jiang X, Sun D, Han G, Wang F, Ye M, Wang L, Zou H", "protein_xref_pubmed", "19159218", "protein_xref_uniprotkb_gly", "Q14126" ], [ "Q14126-1", "", "Human plasma N-glycoproteome analysis by immunoaffinity subtraction, hydrazide chemistry, and mass spectrometry.", "Journal of proteome research", "2005 Nov-Dec", "Liu T, Qian WJ, Gritsenko MA, Camp DG 2nd, Monroe ME, Moore RJ, Smith RD", "protein_xref_pubmed", "16335952", "protein_xref_uniprotkb_gly", "Q14126" ], [ "Q14126-1", "", "Mass-spectrometric identification and relative quantification of N-linked cell surface glycoproteins.", "Nature biotechnology", "2009 Apr", "Wollscheid B, Bausch-Fluck D, Henderson C, O'Brien R, Bibel M, Schiess R, Aebersold R, Watts JD", "protein_xref_pubmed", "19349973", "protein_xref_uniprotkb_gly", "Q14126" ], [ "Q9UKX5-1", "", "Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.", "Journal of proteome research", "2009 Feb", "Chen R, Jiang X, Sun D, Han 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"Identification and quantification of N-linked glycoproteins using hydrazide chemistry, stable isotope labeling and mass spectrometry.", "Nature biotechnology", "2003 Jun", "Zhang H, Li XJ, Martin DB, Aebersold R", "protein_xref_pubmed", "12754519", "protein_xref_uniprotkb_gly", "Q9BVK6" ] ] }, "readme": "Name\n - Human Proteoform Glycosylation Citations (UniProtKB)\n\nVersion\n - 1.11.2\n\nCreated on\n - 2021-06-03T16:32:02.053252\n\nModified on\n - 2022-01-05T14:11:28.778364\n\nCreated by\n - Jeet Vora [jeetvora@gwu.edu], Karina Martinez [karinamartinez@gwu.edu], Amanda Bell [amandab2140@gwu.edu], Jonathon Keeney [keeneyjg@gwu.edu], Millicent Quartey [mquartey@email.gwu.edu]\n\nAuthors\n - \n\nChecksum\n - \n\nExecution Domain\n Scripts\n\n Software Prerequisites\n\nI/O Domain\n Output Subdomain\n Name: human_proteoform_citations_glycosylation_uniprotkb.csv\n URI: http://data.glygen.org/ln2wwwdata/reviewed/human_proteoform_citations_glycosylation_uniprotkb.csv\n Name: human_proteoform_citations_glycosylation_uniprotkb.stat.csv\n URI: http://data.glygen.org/ln2wwwdata/reviewed/human_proteoform_citations_glycosylation_uniprotkb.stat.csv\n\nFields\n Name: \"uniprotkb_canonical_ac\"\n Description: \"\"\n Unique Values: \"16\"\n Name: \"motif_start\"\n Description: \"\"\n Unique Values: \"23\"\n Name: \"filter_flags\"\n Description: \"Filter tags/flags assigned to the mutation entries that have passed the mutation filter criteria\"\n Unique Values: \"19\"\n Name: \"sift_prediction\"\n Description: \"The SIFT qualitative prediction is derived from this score such that substitutions with a score < 0.05 are called 'deleterious' and all others are called 'tolerated\"\n Unique Values: \"3\"\n Name: \"somatic_status\"\n Description: \"The status of the variant whether it is germline (somatic status =0) or somatic (somatic status =1) variant\"\n Unique Values: \"1\"\n Name: \"chr_pos\"\n Description: \"Chromosome Position of a gene\"\n Unique Values: \"19\"\n Name: \"chr_id\"\n Description: \"\"\n Unique Values: \"10\"\n Name: \"dbsnp_id\"\n Description: \"\"A reference SNP ID number\"\n Unique Values: \"19\"\n Name: \"evidence_ECO:0000313\"\n Description: \"A type of evidence that is imported information used in an automatic assertion\"\n Unique Values: \"1\"\n Name: \"xref_id\"\n Description: \"ID of the X-ref\"\n Unique Values: \"19\"\n Name: \"mim_id\"\n Description: \"Disease ID from the OMIM database\"\n Unique Values: \"1\"\n Name: \"description\"\n Description: \"\"\n Unique Values: \"1\"\n Name: \"begin_aa_pos\"\n Description: \"Start position of the amino acid in the sequence of a protein in UniProtKB\"\n Unique Values: \"18\"\n Name: \"cytogenic_band\"\n Description: \"One of the subregions of a chromosome visible microscopically after special staining\"\n Unique Values: \"14\"\n Name: \"aa_pos\"\n Description: \"Position of the amino acid in canonical sequence of protein in the UniProtKB database\"\n Unique Values: \"18\"\n Name: \"ref_aa\"\n Description: \"Reference amino acid residue\"\n Unique Values: \"9\"\n Name: \"sift_score\"\n Description: \"SIFT predicts whether an amino acid substitution is likely to affect protein function based on sequence homology and the physico-chemical similarity between the alternate amino acids. The data we provide for each amino acid substitution is a score and a qualitative prediction (either 'tolerated' or 'deleterious'). The score is the normalized probability that the amino acid change is tolerated so scores nearer zero are more likely to be deleterious. The qualitative prediction is derived from this score such that substitutions with a score < 0.05 are called 'deleterious' and all others are called 'tolerated\"\n Unique Values: \"10\"\n Name: \"alt_motif\"\n Description: \"Altered motif\"\n Unique Values: \"24\"\n Name: \"disease_xrefs\"\n Description: \"\"\n Unique Values: \"1\"\n Name: \"polyphen_score\"\n Description: \"The score assigned to a amino acid substitution by a tool called as PolyPhen (=Polymorphism Phenotyping) which predicts possible impact of an amino acid substitution on the structure and function of a human protein using straightforward physical and comparative considerations. The PolyPhen score ranges from 0.0 (tolerated) to 1.0 (deleterious). Variants with scores of 0.0 are predicted to be benign. Values closer to 1.0 are more confidently predicted to be deleterious\"\n Unique Values: \"1\"\n Name: \"polyphen_prediction\"\n Description: \"\"The PolyPhen prediction values are - greater than 0.908 - \"\"Probably Damaging\"\"; greater than 0.446 and less than or equal to 0.908 - \"\"Possibly Damaging\"\"; less than or equal to 0.446 - \"\"Benign\"\"\"\n Unique Values: \"1\"\n Name: \"is_known_glycoprotein\"\n Description: \"Yes or no flag to denote if a protein is experimentally proven glycoprotein\"\n Unique Values: \"1\"\n Name: \"alt_nt\"\n Description: \"Alternative nucleotide\"\n Unique Values: \"1\"\n Name: \"protein_name\"\n Description: \"Protein name in the UniProtKB\"\n Unique Values: \"16\"\n Name: \"disease_evidence_ECO:0000313\"\n Description: \"The evidence that could be a PMID or a ClinVar ID that associates disease with the variant\"\n Unique Values: \"1\"\n Name: \"effect\"\n Description: \"The effect on glycosylation or N-sequon due to variation at site of glycosylated amino acid.\"\n Unique Values: \"3\"\n Name: \"end_aa_pos\"\n Description: \"End position of the amino acid in the sequence of a protein in UniProtKB\"\n Unique Values: \"18\"\n Name: \"mutation_type\"\n Description: \"Denotes whether mutation was reported with reference to amino acid or nucleotide\"\n Unique Values: \"1\"\n Name: \"disease_description\"\n Description: \"The disease description and/or definition \"\n Unique Values: \"1\"\n Name: \"do_id\"\n Description: \"Disease Ontology identifier\"\n Unique Values: \"1\"\n Name: \"evidence_ECO:0000269\"\n Description: \"A type of experimental evidence that is used in a manual assertion. Usually the values are PMIDs\"\n Unique Values: \"1\"\n Name: \"ref_nt\"\n Description: \"Reference nucleotide\"\n Unique Values: \"4\"\n Name: \"disease\"\n Description: \"The disease name for the cell line\"\n Unique Values: \"1\"\n Name: \"alt_aa\"\n Description: \"Altered amino acid residue\"\n Unique Values: \"10\"\n Name: \"cosmic_id\"\n Description: \"Legacy mutation identifier (COSM) in Catalogue of Somatic Mutations in Cancer (COSMIC) represents existing COSM mutation identifiers. This identifier remains the same between different assemblies (GRCh37 and GRCh38). All the COSM ids at the same genomic location have been collapsed into one representative COSM id. These ids are maintained to help track existing mutations\"\n Unique Values: \"1\"\n Name: \"ref_motif\"\n Description: \"Reference motif\"\n Unique Values: \"20\"\n Name: \"xref_key\"\n Description: \"Source key associated to the xref_id\"\n Unique Values: \"2\"\n Name: \"minor_allelic_frequency\"\n Description: \"\"\n Unique Values: \"1\"\n Name: \"gene_name\"\n Description: \"\"Official gene name/symbol assigned to the gene. Human gene name/symbol are approved by the HUGO Gene Nomenclature Committee (HGNC) and mouse gene name are approved by the Mouse Genome Informatics (MGI)\"\n Unique Values: \"17\"\n Name: \"disease_evidence_ECO:0000269\"\n Description: \"The PMID evidence for the association of the disease with the variant.\"\n Unique Values: \"1\"", "downloadurl": "/ln2data/releases/data/v-1.11.2/reviewed/human_proteoform_citations_glycosylation_uniprotkb.csv" }