{
    "bcoid": "GLY_000035",
    "title": "Human Protein Citations (UniProtKB)",
    "description": "The Human Protein Citations dataset contains publication information for human [taxid:9606] UniProtKB ...",
    "filename": "human_protein_citations_uniprotkb.csv",
    "filetype": "csv",
    "categories": {
        "species": "Homo sapiens",
        "molecule": "Protein",
        "tags": "Protein Citations",
        "file_type": "csv",
        "status": "Reviewed",
        "scope": "internal"
    },
    "minitable": {
        "content": [
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                "P30613-1...",
                "Hematologica..."
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                "P30613-1...",
                "Hematologica..."
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            [
                "P30613-1",
                "Hematologically important mutations: red cell pyruvate kinase (2nd update).",
                "Blood Cells Mol. Dis.",
                "1998",
                "Bianchi P., Zanella A., Baronciani L.",
                "protein_xref_pubmed",
                "10087985",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Hematologically important mutations: red cell pyruvate kinase (third update).",
                "Blood Cells Mol. Dis.",
                "2000",
                "Bianchi P., Zanella A.",
                "protein_xref_pubmed",
                "10772876",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Molecular characterization of the PK-LR gene in sixteen pyruvate kinase-deficient patients.",
                "Br. J. Haematol.",
                "2001",
                "Bianchi P., Fermo E., Vercellati C., Zanella A., Baronciani L., Cotton F., Zappa M., Boschetti C., Iurlo A.",
                "protein_xref_pubmed",
                "11328279",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Structure and function of human erythrocyte pyruvate kinase. Molecular basis of nonspherocytic hemolytic anemia.",
                "J. Biol. Chem.",
                "2002",
                "Wang C., Bianchi P., Chiarelli L.R., Galizzi A., Mattevi A., Valentini G., Zanella A., Abraham D.J., Dolzan M., Fortin R.",
                "protein_xref_pubmed",
                "11960989",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Structural analysis of human pyruvate kinase L-gene and identification of the promoter activity in erythroid cells.",
                "Biochem. Biophys. Res. Commun.",
                "1992",
                "Fujii H., Kanno H., Miwa S.",
                "protein_xref_pubmed",
                "1445295",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Identical point mutations of the R-type pyruvate kinase (PK) cDNA found in unrelated PK variants associated with hereditary hemolytic anemia.",
                "Blood",
                "1992",
                "Fujii H., Kanno H., Miwa S., Hirono A., Omine M.",
                "protein_xref_pubmed",
                "1536957",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "cDNA cloning of human R-type pyruvate kinase and identification of a single amino acid substitution (Thr384-->Met) affecting enzymatic stability in a pyruvate kinase variant (PK Tokyo) associated with hereditary hemolytic anemia.",
                "Proc. Natl. Acad. Sci. U.S.A.",
                "1991",
                "Fujii H., Kanno H., Miwa S., Hirono A.",
                "protein_xref_pubmed",
                "1896471",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Fifteen novel mutations in PKLR associated with pyruvate kinase (PK) deficiency: structural implications of amino acid substitutions in PK.",
                "Hum. Mutat.",
                "2009",
                "Huizinga E.G., Hadders M.A., van Solinge W.W., van Wijk R., van Oirschot B.A., van Wesel A.C.W.",
                "protein_xref_pubmed",
                "19085939",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Point mutations in the L-type pyruvate kinase gene of two children with hemolytic anemia caused by pyruvate kinase deficiency.",
                "Blood",
                "1991",
                "Winkler H., Neubauer B., Hofferbert S., Lakomek M., Schroter W., Parke M.",
                "protein_xref_pubmed",
                "2018831",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications.",
                "Discov. Med.",
                "2011",
                "Lin Y., Liu Y., Tian L., Wang J., Wang W., Wei Z., Zhang P., Lyon G.J., Hakonarson H., Johnson W.E., Wang K., Jiang T., Moore B., Yandell M., Glessner J.T., Xing J., van Solinge W.W., Reimherr F., Bodily P.M., Clement M., Elia J., Robison R.J., Van Wijk R.",
                "protein_xref_pubmed",
                "21794208",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Human liver type pyruvate kinase: complete amino acid sequence and the expression in mammalian cells.",
                "Proc. Natl. Acad. Sci. U.S.A.",
                "1988",
                "Nagata S., Tani K., Fujii H., Miwa S.",
                "protein_xref_pubmed",
                "3126495",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Human liver type pyruvate kinase: cDNA cloning and chromosomal assignment.",
                "Biochem. Biophys. Res. Commun.",
                "1987",
                "Tanaka T., Yoshida M.C., Tani K., Fujii H., Miwa S., Noguchi T., Toyoshima K., Tsutsumi H., Sukegawa J.",
                "protein_xref_pubmed",
                "3566732",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia.",
                "J. Clin. Invest.",
                "1995",
                "Beutler E., Baronciani L.",
                "protein_xref_pubmed",
                "7706479",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Molecular abnormality of erythrocyte pyruvate kinase deficiency in the Amish.",
                "Blood",
                "1994",
                "Fujii H., Kanno H., Miwa S., Ballas S.K., Bowman H.S.",
                "protein_xref_pubmed",
                "8161798",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia.",
                "Blood",
                "1994",
                "Nuernberg P., Reis A., Brabec V., Jacobasch G., Lenzner C., Sakalova A., Thiele B.-J.",
                "protein_xref_pubmed",
                "8180378",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Molecular basis of impaired pyruvate kinase isozyme conversion in erythroid cells: a single amino acid substitution near the active site and decreased mRNA content of the R-type PK.",
                "Biochem. Biophys. Res. Commun.",
                "1993",
                "Fujii H., Kanno H., Miwa S., Tsujino G.",
                "protein_xref_pubmed",
                "8476433",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Low substrate affinity of pyruvate kinase variant (PK Sapporo) caused by a single amino acid substitution (426 Arg-->Gln) associated with hereditary hemolytic anemia.",
                "Blood",
                "1993",
                "Fujii H., Kanno H., Miwa S.",
                "protein_xref_pubmed",
                "8481523",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia.",
                "Proc. Natl. Acad. Sci. U.S.A.",
                "1993",
                "Beutler E., Baronciani L.",
                "protein_xref_pubmed",
                "8483951",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Mutations in pyruvate kinase.",
                "Hum. Mutat.",
                "1996",
                "Beutler E., Baronciani L.",
                "protein_xref_pubmed",
                "8664896",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Hematologically important mutations: red cell pyruvate kinase.",
                "Blood Cells Mol. Dis.",
                "1996",
                "Bianchi P., Zanella A., Baronciani L.",
                "protein_xref_pubmed",
                "8807089",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Hematologically important mutations: red cell pyruvate kinase (1st update).",
                "Blood Cells Mol. Dis.",
                "1996",
                "Bianchi P., Zanella A., Baronciani L.",
                "protein_xref_pubmed",
                "9075576",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "G-to-T transition at cDNA nt 110 (K37Q) in the PKLR (pyruvate kinase) gene is the molecular basis of a case of hereditary increase of red blood cell ATP.",
                "Hum. Mutat.",
                "1997",
                "Beutler E., Roos D., van Zwieten R., Westwood B.",
                "protein_xref_pubmed",
                "9090535",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Novel mutations and structural implications in R-type pyruvate kinase-deficient patients from Southern Italy.",
                "Hum. Mutat.",
                "1998",
                "Alfinito F., Ferraro F., Rotoli B., Salvatore F., Zagari A., Vitale D., Pastore L., Calise R.M., Frisso G., della Morte R.",
                "protein_xref_pubmed",
                "9482576",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "Molecular characterization of the PK-LR gene in pyruvate kinase deficient Spanish patients.",
                "Br. J. Haematol.",
                "1998",
                "Alvarez R., Morey M., Vives Corrons J.L., Remacha A., Bureo E., Carrera A., Cortes T., Estella J., Nomdedeu B., Perez Lungmus G., Pujades A., Sanchez J.M., Zarza R.",
                "protein_xref_pubmed",
                "9827908",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P30613-1",
                "A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha-2 globin gene variant (Hb Conakry).",
                "Br. J. Haematol.",
                "1998",
                "Wajcman H., Cohen-Solal M., Bardakdjian-Michau J., Galacteros F., Kister J., Poyart C., Prehu C., Prome D., Bachir D., Valentin C.",
                "protein_xref_pubmed",
                "9886305",
                "protein_xref_uniprotkb",
                "P30613"
            ],
            [
                "P23919-1",
                "Lysine acetylation targets protein complexes and co-regulates major cellular functions.",
                "Science",
                "2009",
                "Choudhary C., Gnad F., Kumar C., Mann M., Nielsen M.L., Olsen J.V., Rehman M., Walther T.C.",
                "protein_xref_pubmed",
                "19608861",
                "protein_xref_uniprotkb",
                "P23919"
            ],
            [
                "P23919-1",
                "Structures of human thymidylate kinase in complex with prodrugs: implications for the structure-based design of novel compounds.",
                "Biochemistry",
                "2003",
                "Konrad M., Meier C., Lavie A., Ostermann N., Monnerjahn C., Segura-Pena D., Veit T.",
                "protein_xref_pubmed",
                "12614151",
                "protein_xref_uniprotkb",
                "P23919"
            ],
            [
                "P23919-1",
                "Human thymidylate kinase. Purification, characterization, and kinetic behavior of the thymidylate kinase derived from chronic myelocytic leukemia.",
                "J. Biol. Chem.",
                "1977",
                "Cheng Y., Lee L.S.",
                "protein_xref_pubmed",
                "18469",
                "protein_xref_uniprotkb",
                "P23919"
            ],
            [
                "P23919-1",
                "Molecular cloning and expression of the human deoxythymidylate kinase gene in yeast.",
                "Nucleic Acids Res.",
                "1991",
                "Sclafani R.A., Su J.Y.",
                "protein_xref_pubmed",
                "2017365",
                "protein_xref_uniprotkb",
                "P23919"
            ],
            [
                "P23919-1",
                "Human dTMP kinase: gene expression and enzymatic activity coinciding with cell cycle progression and cell growth.",
                "DNA Cell Biol.",
                "1994",
                "Li C., Tang A., Zhang S.Q., Drisco B., Huang S.H., Jong A., Seeger R.",
                "protein_xref_pubmed",
                "8024690",
                "protein_xref_uniprotkb",
                "P23919"
            ],
            [
                "P23919-1",
                "Deoxythymidylate kinase, DTYMK, is a novel gene for mitochondrial DNA depletion syndrome.",
                "Clin. Chim. Acta",
                "2019",
                "Lam C.W., Law C.Y., Wong K.C., Yeung W.L., Ling T.K.",
                "protein_xref_pubmed",
                "31271740",
                "protein_xref_uniprotkb",
                "P23919"
            ],
            [
                "P23919-1",
                "DTYMK is essential for genome integrity and neuronal survival.",
                "Acta Neuropathol.",
                "2022",
                "Wang L., Rodenburg R., Brunner H.G., Wevers R.A., Abdel-Salam G.M.H., Kamsteeg E.J., O'Driscoll M., Bugiani M., Colnaghi R., van den Wijngaard A., van der Knaap M.S., Bierau J., Ferreira C.R., Bok L.A., Stumpel C.T.R.M., Frisk J.H., Grashorn J.C., Hellebrekers D.M.E.I., Lambrichs E., Vanoevelen J.M.",
                "protein_xref_pubmed",
                "34918187",
                "protein_xref_uniprotkb",
                "P23919"
            ],
            [
                "Q8NHX4-1",
                "Molecular cloning for testis spermatogenesis cell apoptosis related gene TSARG1 and Mtsarg1 and expression analysis for Mtsarg1 gene.",
                "Yi Chuan Xue Bao",
                "2003",
                "Liu G., Li L.Y., Lu G.X., Xing X.W., Fu J.J., Liu S.F.",
                "protein_xref_pubmed",
                "12812072",
                "protein_xref_uniprotkb",
                "Q8NHX4"
            ],
            [
                "Q8NHX9-1",
                "Two newly identified genetic determinants of pigmentation in Europeans.",
                "Nat. Genet.",
                "2008",
                "Gudbjartsson D.F., Jakobsdottir M., Kiemeney L.A., Kong A., Rafnar T., Stacey S.N., Stefansson K., Steinberg S., Sulem P., Thorleifsson G., Thorsteinsdottir U., Gudjonsson S.A., Tucker M.A., Palsson S., Goldstein A.M., Aben K.K., Benediktsdottir K.R., Vermeulen S.H., Helgason A., Gulcher J., Olafsson J.H., Palsson A., Ragnarsson R., Sigurgeirsson B., Thorisdottir K.",
                "protein_xref_pubmed",
                "18488028",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "NAADP mobilizes calcium from acidic organelles through two-pore channels.",
                "Nature",
                "2009",
                "Lin Y., Ma J., Pan Z., Tang J., Wang C., Zhu Y., Cheng X., Hao X., Lin P., Xiao R., Rietdorf K., Zhu M.X., Ruas M., Evans A.M., Parrington J., Galione A., Arredouani A., Calcraft P.J., Chuang K.T., Teboul L., Wyatt C.N.",
                "protein_xref_pubmed",
                "19387438",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Essential requirement for two-pore channel 1 in NAADP-mediated calcium signaling.",
                "J. Cell Biol.",
                "2009",
                "Gao X., Cai X., Patel S., Brailoiu E., Brailoiu G.C., Dun N.J., Churamani D., Marchant J.S., Boulware M.J., Hooper R., Schrlau M.G.",
                "protein_xref_pubmed",
                "19620632",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Leucine-rich repeat kinase 2 regulates autophagy through a calcium-dependent pathway involving NAADP.",
                "Hum. Mol. Genet.",
                "2012",
                "Zhang L., Patel S., Woodman P.G., Churchill G.C., Bloor-Young D., Churamani D., Gomez-Suaga P., Hilfiker S., Luzon-Toro B.",
                "protein_xref_pubmed",
                "22012985",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Hax-1 identified as a two-pore channel (TPC)-binding protein.",
                "FEBS Lett.",
                "2013",
                "Lai F.A., Galione A., Lam A.K., Zissimopoulos S.",
                "protein_xref_pubmed",
                "24188827",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "TPC2 controls pigmentation by regulating melanosome pH and size.",
                "Proc. Natl. Acad. Sci. U.S.A.",
                "2016",
                "Di Pietro S.M., Ambrosio A.L., Aradi A.E., Boyle J.A., Christian K.A.",
                "protein_xref_pubmed",
                "27140606",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV.",
                "Nat. Commun.",
                "2020",
                "Chen J., Chen X., Li P., Liu Y., Wang J., Chen T., Hu J., Hu K., Guo L., Jin Q., Lei X., Guo R., Qian Z., Ren L., Ou X., Xiang Z., Mi D., Mu Z.",
                "protein_xref_pubmed",
                "32221306",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "mTOR regulates lysosomal ATP-sensitive two-pore Na(+) channels to adapt to metabolic state.",
                "Cell",
                "2013",
                "Zhou Y., Shi L., Clapham D.E., Ren D., Navarro B., Aranda K., Cang C., Seo Y.J., Nissim I., Battaglia-Hsu S.",
                "protein_xref_pubmed",
                "23394946",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "An NAADP-gated two-pore channel targeted to the plasma membrane uncouples triggering from amplifying Ca2+ signals.",
                "J. Biol. Chem.",
                "2010",
                "Patel S., Rahman T., Brailoiu E., Brailoiu G.C., Churamani D., Hooper R., Taylor C.W., Prole D.L.",
                "protein_xref_pubmed",
                "20880839",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "TPC proteins are phosphoinositide- activated sodium-selective ion channels in endosomes and lysosomes.",
                "Cell",
                "2012",
                "Li X., Wang X., Xu H., Zhang X., Zhou Y., Cheng X., Clapham D.E., Zhu M.X., Ren D., Shen D., Dong X.P., Goschka A., Samie M., Harlow J.",
                "protein_xref_pubmed",
                "23063126",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Convergent regulation of the lysosomal two-pore channel-2 by Mg(2+), NAADP, PI(3,5)P(2) and multiple protein kinases.",
                "EMBO J.",
                "2014",
                "Patel S., Muallem S., Ahuja M., Jha A., Brailoiu E.",
                "protein_xref_pubmed",
                "24502975",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "The voltage-gated sodium channel TPC1 confers endolysosomal excitability.",
                "Nat. Chem. Biol.",
                "2014",
                "Ren D., Cang C., Bekele B.",
                "protein_xref_pubmed",
                "24776928",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Ebola virus. Two-pore channels control Ebola virus host cell entry and are drug targets for disease treatment.",
                "Science",
                "2015",
                "Grimm C., Klugbauer N., Sakurai Y., Chen C.C., Biel M., Davey R.A., Wahl-Schott C., Kolokoltsov A.A., Bauta W.E., Tidwell M.W.",
                "protein_xref_pubmed",
                "25722412",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Targeting Two-Pore Channels: Current Progress and Future Challenges.",
                "Trends Pharmacol. Sci.",
                "2020",
                "Zhang Y., Jin X., Parrington J., Alharbi A., Alhoshani A., Hanbashi A.",
                "protein_xref_pubmed",
                "32679067",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Author Correction: Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV.",
                "Nat. Commun.",
                "2021",
                "Chen J., Chen X., Li P., Liu Y., Wang J., Chen T., Hu J., Hu K., Guo L., Jin Q., Lei X., Guo R., Qian Z., Ren L., Ou X., Xiang Z., Mi D., Mu Z.",
                "protein_xref_pubmed",
                "33795662",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q8NHX9-1",
                "Lsm12 is an NAADP receptor and a two-pore channel regulatory protein required for calcium mobilization from acidic organelles.",
                "Nat. Commun.",
                "2021",
                "Zhang J., Yan J., Guan X., Shah K.",
                "protein_xref_pubmed",
                "34362892",
                "protein_xref_uniprotkb",
                "Q8NHX9"
            ],
            [
                "Q9C0H5-1",
                "Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.",
                "Mol. Cell",
                "2008",
                "Bairlein M., Daub H., Gnad F., Greff Z., Keri G., Korner R., Mann M., Olsen J.V., Oppermann F.S., Stemmann O.",
                "protein_xref_pubmed",
                "18691976",
                "protein_xref_uniprotkb",
                "Q9C0H5"
            ],
            [
                "Q9C0H9-5",
                "p140Cap protein suppresses tumour cell properties, regulating Csk and Src kinase activity.",
                "EMBO J.",
                "2007",
                "Silengo L., Tarone G., Turco E., Aramu S., Cabodi S., Cavallo F., Damiano L., Defilippi P., Di Stefano P., Forni G., Piva R., Praduroux A., Tordella L.",
                "protein_xref_pubmed",
                "17525734",
                "protein_xref_uniprotkb",
                "Q9C0H9"
            ],
            [
                "Q9C0H9-5",
                "p130Cas-associated protein (p140Cap) as a new tyrosine-phosphorylated protein involved in cell spreading.",
                "Mol. Biol. Cell",
                "2004",
                "Silengo L., Tarone G., Turco E., Cabodi S., Defilippi P., Di Stefano P., Giuffrida M.G., Bergatto E., Erba E.B., Margaria V.",
                "protein_xref_pubmed",
                "14657239",
                "protein_xref_uniprotkb",
                "Q9C0H9"
            ],
            [
                "Q9C0H9-5",
                "SNIP/p140Cap mRNA expression is an unfavourable prognostic factor in breast cancer and is not expressed in normal breast tissue.",
                "Br. J. Cancer",
                "2008",
                "Kennedy S., Clynes M., Crown J., Doolan P., Mehta J.P., O'Driscoll L., Rani S.",
                "protein_xref_pubmed",
                "18475297",
                "protein_xref_uniprotkb",
                "Q9C0H9"
            ],
            [
                "Q9C0H9-5",
                "Characterization of a multidomain adaptor protein, p140Cap, as part of a pre-synaptic complex.",
                "J. Neurochem.",
                "2008",
                "Ito H., Morishita R., Usuda N., Nagata K., Sudo K., Asano T., Iwamoto I., Defilippi P., Di Stefano P., Atsuzawa K., Semba R., Takei S.",
                "protein_xref_pubmed",
                "18662323",
                "protein_xref_uniprotkb",
                "Q9C0H9"
            ],
            [
                "Q9C0H9-5",
                "Dynamic microtubules regulate dendritic spine morphology and synaptic plasticity.",
                "Neuron",
                "2009",
                "Grigoriev I., Akhmanova A., Gouveia S.M., Hoogenraad C.C., Demmers J., Kapitein L.C., Wulf P.S., Jaworski J., Camera P., Defilippi P., Di Stefano P., Dortland B.R., Spangler S.A., Krugers H.",
                "protein_xref_pubmed",
                "19146815",
                "protein_xref_uniprotkb",
                "Q9C0H9"
            ],
            [
                "Q96J66-1",
                "Two new genes from the human ATP-binding cassette transporter superfamily, ABCC11 and ABCC12, tandemly duplicated on chromosome 16q12.",
                "Gene",
                "2001",
                "Allikmets R., Arnould I., Dean M., Prades C., Rosier M., Hutchinson A., Schuetz J.D., Tammur J., Adachi M., Ptacek L.J., Rzhetsky A., Swoboda K.J.",
                "protein_xref_pubmed",
                "11483364",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "MRP8, a new member of ABC transporter superfamily, identified by EST database mining and gene prediction program, is highly expressed in breast cancer.",
                "Mol. Med.",
                "2001",
                "Lee S., Bera T.K., Lee B.K., Pastan I.H., Salvatore G.",
                "protein_xref_pubmed",
                "11591886",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "Multiple splicing variants of two new human ATP-binding cassette transporters, ABCC11 and ABCC12.",
                "Biochem. Biophys. Res. Commun.",
                "2001",
                "Shimizu H., Ishikawa T., Takayanagi S., Yabuuchi H.",
                "protein_xref_pubmed",
                "11688999",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "MRP8, ATP-binding cassette C11 (ABCC11), is a cyclic nucleotide efflux pump and a resistance factor for fluoropyrimidines 2',3'-dideoxycytidine and 9'-(2'-phosphonylmethoxyethyl)adenine.",
                "J. Biol. Chem.",
                "2003",
                "Kruh G.D., Belinsky M.G., Guo Y., Chen Z.S., Hopper-Borge E., Kotova E., Lee K.",
                "protein_xref_pubmed",
                "12764137",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "Transport of bile acids, sulfated steroids, estradiol 17-beta-D-glucuronide, and leukotriene C4 by human multidrug resistance protein 8 (ABCC11).",
                "Mol. Pharmacol.",
                "2005",
                "Kruh G.D., Belinsky M.G., Guo Y., Chen Z.S., Kotova E.",
                "protein_xref_pubmed",
                "15537867",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "Human multidrug resistance protein 8 (MRP8/ABCC11), an apical efflux pump for steroid sulfates, is an axonal protein of the CNS and peripheral nervous system.",
                "Neuroscience",
                "2006",
                "Nies A.T., Koenig J., Keppler D., Rius M., Bortfeld M., Herold-Mende C.",
                "protein_xref_pubmed",
                "16359813",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "A SNP in the ABCC11 gene is the determinant of human earwax type.",
                "Nat. Genet.",
                "2006",
                "Nakamura Y., Saitou N., Takahashi H., Bannai M., Ishikawa T., Kim D.-K., Saito S., Tokunaga K., Ohta T., Sonoda S., Komatsu K., Murray J.C., Niikawa N., Alipov G.K., Garidkhuu A., Ghadami M., Hirayama K., Ihara M., Ishibashi M., Ishida T., Kaname T., Kaneko A., Kikuchi M., Kinoshita A., Komaki R., Liang D.-S., Mapendano C.K., Miwa N., Nakashima M., Natsume N., Ninokata A., Nomura M., Russomando G., Saenko V.A., Sekine I., Sosonkina N., Takahashi A., Tomita H., Yoshiura K.",
                "protein_xref_pubmed",
                "16444273",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "Earwax, osmidrosis, and breast cancer: why does one SNP (538G>A) in the human ABC transporter ABCC11 gene determine earwax type?",
                "FASEB J.",
                "2009",
                "Ishikawa T., Nakagawa H., Sakai Y., Niikawa N., Hayashizaki Y., Lezhava A., Mitani Y., Nakashima M., Ota I., Sakurai A., Toyoda Y., Yoshiura K.",
                "protein_xref_pubmed",
                "19383836",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "A functional ABCC11 allele is essential in the biochemical formation of human axillary odor.",
                "J. Invest. Dermatol.",
                "2010",
                "Kuhn F., Martin A., Max H., Natsch A., Saathoff M., Terstegen L.",
                "protein_xref_pubmed",
                "19710689",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q96J66-1",
                "Functional characterization of common protein variants in the efflux transporter ABCC11 and identification of T546M as functionally damaging variant.",
                "Pharmacogenomics J.",
                "2016",
                "Ishikawa T., Lang T., Schaeffeler E., Arlanov R., Jedlitschky G., Nies A.T., Schwab M.",
                "protein_xref_pubmed",
                "25896536",
                "protein_xref_uniprotkb",
                "Q96J66"
            ],
            [
                "Q8NC06-1",
                "Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.",
                "Cell",
                "2016",
                "Yang X., Yi S., Tam S., Yang F., Vidal M., Richardson A., Xia Y., Zhong Q., Hill D.E., Sun S., Calderwood M.A., Ghamsari L., Hao T., Iakoucheva L.M., Kang S., Roth F.P., Salehi-Ashtiani K., Chen A., Aloy P., Tan G., Andrews B., Murray R., Boone C., Costanzo M., Zhou X.J., Balcha D., Begg B.E., Charloteaux B., Coulombe-Huntington J., Duran-Frigola M., MacWilliams A., Pevzner S.J., Rodriguez M.D., Sahni N., Shen Y.A., Sheynkman G.M., Spirohn K., Trigg S.A.",
                "protein_xref_pubmed",
                "26871637",
                "protein_xref_uniprotkb",
                "K7EM05"
            ],
            [
                "Q14766-1",
                "Phosphoproteome of resting human platelets.",
                "J. Proteome Res.",
                "2008",
                "Gambaryan S., Lewandrowski U., Moebius J., Schuetz C., Sickmann A., Walter U., Wiesner J., Wortelkamp S., Zahedi R.P., Schutz C.",
                "protein_xref_pubmed",
                "18088087",
                "protein_xref_uniprotkb",
                "E7EV71"
            ],
            [
                "P40424-1",
                "Analysis of PBX1 as a candidate gene for type 2 diabetes mellitus in Pima Indians.",
                "Biochim. Biophys. Acta",
                "2001",
                "Bogardus C., Prochazka M., Wolford J.K., Thameem F.",
                "protein_xref_pubmed",
                "11267683",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias.",
                "Blood",
                "1991",
                "Cleary M.L., Crist W.M., Hunger S.P., Galili N., Carroll A.J., Link M.P.",
                "protein_xref_pubmed",
                "1671560",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL.",
                "Cell",
                "1990",
                "Baltimore D., Kamps M.P., Sun X.-H., Murre C.",
                "protein_xref_pubmed",
                "1967983",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans.",
                "J. Med. Genet.",
                "2017",
                "Breton J., Dieterich K., Jouk P.S., Odent S., Digilio M.C., Harbuz R., Ray P.F., Coutton C., Vieville G., Apostolou A., Mackenroth L., Vogel I., Fokstuen S., Satre V., Bidart M., Le Tanno P., Devillard F., Bosson C., Jaillard S., Pisanti M.A., Bernardini L., Amblard F., Beddow R., Bena F., Christensen R., Guebre-Egziabher F., Hackmann K., Novelli A., Poke G., Sartelet H.",
                "protein_xref_pubmed",
                "28270404",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Targeted exome sequencing identifies PBX1 as involved in monogenic congenital anomalies of the kidney and urinary tract.",
                "J. Am. Soc. Nephrol.",
                "2017",
                "Salomon R., Antignac C., Gonzales M., Roume J., Nitschke P., Schaefer E., Bras M., Gaillard D., Saunier S., Henry C., Jeanpierre C., Martinovic J., Bole-Feysot C., Jeanpierre M., Heidet L., Alibeu O., Novo R., Pietrement C., Fourrage C., Tores F., Moriniere V., Humbert C., Malan V., De Tomasi L., Reilly M.L.",
                "protein_xref_pubmed",
                "28566479",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Pbx1 is converted into a transcriptional activator upon acquiring the N-terminal region of E2A in pre-B-cell acute lymphoblastoid leukemia.",
                "Proc. Natl. Acad. Sci. U.S.A.",
                "1993",
                "Voorhoeve P.M., van Dijk M.A., Murre C.",
                "protein_xref_pubmed",
                "8327485",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Structure of a HoxB1-Pbx1 heterodimer bound to DNA: role of the hexapeptide and a fourth homeodomain helix in complex formation.",
                "Cell",
                "1999",
                "Cleary M.L., Wolberger C., Piper D.E., Batchelor A.H., Chang C.-P.",
                "protein_xref_pubmed",
                "10052460",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Cooperative transcriptional activation by Klf4, Meis2, and Pbx1.",
                "Mol. Cell. Biol.",
                "2011",
                "Wotton D., Bjerke G.A., Hyman-Walsh C.",
                "protein_xref_pubmed",
                "21746878",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Homeodomain proteins MEIS1 and PBXs regulate the lineage-specific transcription of the platelet factor 4 gene.",
                "Blood",
                "2003",
                "Doi T., Sato T., Matsuura E., Okada Y., Nagai R., Minami T., Morita I.",
                "protein_xref_pubmed",
                "12609849",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "MEIS proteins as partners of the TLX1/HOX11 oncoprotein.",
                "Leuk. Res.",
                "2010",
                "Kees U.R., Ford J., Greene W.K., D'Souza D., Gottardo N.G., Milech N., Watt P.M.",
                "protein_xref_pubmed",
                "19559479",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "An autoinhibitory effect of the homothorax domain of Meis2.",
                "FEBS J.",
                "2010",
                "Wotton D., Bjerke G.A., Hyman-Walsh C.",
                "protein_xref_pubmed",
                "20553494",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner.",
                "Mol. Cell. Biol.",
                "2005",
                "O'Neill M.A., Walter M.A., Coca-Prados M., Berry F.B.",
                "protein_xref_pubmed",
                "15684392",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Functional cloning and characterization of a novel nonhomeodomain protein that inhibits the binding of PBX1-HOX complexes to DNA.",
                "J. Biol. Chem.",
                "2000",
                "Humphries R.K., Largman C., Montpetit B., Shen W.-F., Abramovich C., Imren S., Pineault N.",
                "protein_xref_pubmed",
                "10825160",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "PBX2 and PBX3, new homeobox genes with extensive homology to the human proto-oncogene PBX1.",
                "Mol. Cell. Biol.",
                "1991",
                "Cleary M.L., Galili N., Monica K., Nourse J., Saltman D.",
                "protein_xref_pubmed",
                "1682799",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Fusion with E2A converts the Pbx1 homeodomain protein into a constitutive transcriptional activator in human leukemias carrying the t(1;19) translocation.",
                "Mol. Cell. Biol.",
                "1994",
                "Lu Q., Kamps M.P., Wright D.D.",
                "protein_xref_pubmed",
                "7910944",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "PBX1 and MEIS1 up-regulate SOX3 gene expression by direct interaction with a consensus binding site within the basal promoter region.",
                "Biochem. J.",
                "2009",
                "Stevanovic M., Mojsin M.",
                "protein_xref_pubmed",
                "19799567",
                "protein_xref_uniprotkb",
                "P40424"
            ],
            [
                "P40424-1",
                "Both Pbx1 and E2A-Pbx1 bind the DNA motif ATCAATCAA cooperatively with the products of multiple murine Hox genes, some of which are themselves oncogenes.",
                "Mol. Cell. Biol.",
                "1995",
                "Lu Q., Kamps M.P., Wright D.D., Knoepfler P.S., Scheele J.",
                "protein_xref_pubmed",
                "7791786",
                "protein_xref_uniprotkb",
                "P40424"
            ]
        ]
    },
    "readme": "Name\n   - Human Protein Citations (UniProtKB)\n\nVersion\n   - v-2.0.3\n\nCreated on\n  - 2019-01-23T17:21:05.902655\n\nModified on\n   - 2022-09-26T08:48:18.842206\n\nCreated by\n   - Jeet Vora [jeetvora@gwu.edu], Rahi Navelkar [rsn13@gwu.edu], Robel Kahsay [rykahsay@gwu.edu], Xavier Holmes [xavierh@email.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   - Maria Martin [martin@ebi.ac.uk], Preethi Vasudev [pvasudev@ebi.ac.uk]\n\nChecksum\n   - \n\nUsability Domain\n   - The Human Protein Citations dataset contains publication information for human [taxid:9606] UniProtKB accessions that includes PMID, journal name, date and author and title. Publications of large scale studies, and high frequency publications pertaining to genome sequencing, cDNA, chromosomes have been filtered out as per https://data.glygen.org/ln2data/releases/data/v-1.12.3/compiled/human_protein_blacklisted_pmids_uniprotkb.csv. The dataset is derived from 2019-09 UniProt release. If you use this dataset please provide proper attribution to EMBL-EBI-UniProtKB and GlyGen\n\nDescription Domain\n   Keywords\n   - publications\n   - PMID\n   - journal\n   - citations\n   - authors\n   - UniProtKB\n   - PubMed\n\n   Pipeline Steps\n   - Step-1: The script loads the UniProtKB publication data from the triplestore containing triples from nt file to retrieve the publication information associated with the UniProtKB accession and maps it to the UniProtKB canonical accessions. The script also filters out publications of large scale studies, and high frequency publications pertaining to DNA sequencing, cDNA, chromosomes using blacklisted PMIDs file.\n\nExecution Domain\n   Scripts   - https://github.com/glygener/glygen-backend-integration/blob/master/dataset-maker/make-protein-dataset.py\n\n\n   Software Prerequisites\n      Name: Python\n      Version: 2.7.5\n      URI: https://www.python.org/download/releases/2.7.5/\n\nI/O Domain\n   Input Subdomain\n      Name: human_protein_blacklisted_pmids_uniprotkb.csv\n      URI: https:/data.glygen.org/ln2releases/data/v-2.0.3/compiled/human_protein_blacklisted_pmids_uniprotkb.csv\n      Name: uniprot-proteome-homo-sapiens.nt\n      URI: /data/shared/glyds/downloads/ebi/2022_05/uniprot-proteome-homo-sapiens.nt\n   Output Subdomain\n      Name: human_protein_citations_uniprotkb.csv\n      URI: https:/data.glygen.org/ln2releases/data/v-2.0.3/reviewed/human_protein_citations_uniprotkb.csv\n      Name: human_protein_citations_uniprotkb.stat.csv\n      URI: https:/data.glygen.org/ln2releases/data/v-2.0.3/reviewed/human_protein_citations_uniprotkb.stat.csv\n\nFields\n      Name: \"uniprotkb_canonical_ac\"\n     Description: \"\"\n      Unique Values: \"17564\"\n      Name: \"title\"\n     Description: \"Title of the published article in the journal\"\n      Unique Values: \"82297\"\n      Name: \"journal_name\"\n     Description: \"The name of the journal in which the article is published\"\n      Unique Values: \"1754\"\n      Name: \"publication_date\"\n     Description: \"Contains the full date on which the issue of the journal was published. Sourced from MEDLINE/PubMed data element(fields) description.\"\n      Unique Values: \"63\"\n      Name: \"authors\"\n     Description: \"NA\"\n      Unique Values: \"81135\"\n      Name: \"xref_key\"\n     Description: \"Source key associated to the  xref_id\"\n      Unique Values: \"1\"\n      Name: \"xref_id\"\n     Description: \"ID of the X-ref\"\n      Unique Values: \"82327\"\n      Name: \"src_xref_key\"\n     Description: \"Source Xref  key\"\n      Unique Values: \"1\"\n      Name: \"src_xref_id\"\n     Description: \"Source X-ref ID\"\n      Unique Values: \"24838\"",
    "downloadurl": "/ln2data/releases/data/v-2.0.3/reviewed/human_protein_citations_uniprotkb.csv"
}
