E3 binding protein (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "E3 binding protein" in English language version.

refsWebsite

Global rank English rank

20nih.gov

4^th place

13doi.org

2^nd place

2ensembl.org

1,626^th place

1,007^th place

2semanticscholar.org

11^th place

8^th place

1wikipathways.org

low place

doi.org

Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C (Dec 1997). "Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis". American Journal of Human Genetics. 61 (6): 1318–26. doi:10.1086/301653. PMC 1716072. PMID 9399911.
Ling M, McEachern G, Seyda A, MacKay N, Scherer SW, Bratinova S, Beatty B, Giovannucci-Uzielli ML, Robinson BH (Mar 1998). "Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiency". Human Molecular Genetics. 7 (3): 501–5. doi:10.1093/hmg/7.3.501. PMID 9467010.
Gawin B, Niederführ A, Schumacher N, Hummerich H, Little PF, Gessler M (Nov 1999). "A 7.5 Mb sequence-ready PAC contig and gene expression map of human chromosome 11p13-p14.1". Genome Research. 9 (11): 1074–86. doi:10.1101/gr.9.11.1074. PMC 310838. PMID 10568747.
Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C (Dec 1997). "Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis". American Journal of Human Genetics. 61 (6): 1318–26. doi:10.1086/301653. PMC 1716072. PMID 9399911.
Harris RA, Bowker-Kinley MM, Wu P, Jeng J, Popov KM (Aug 1997). "Dihydrolipoamide dehydrogenase-binding protein of the human pyruvate dehydrogenase complex. DNA-derived amino acid sequence, expression, and reconstitution of the pyruvate dehydrogenase complex". The Journal of Biological Chemistry. 272 (32): 19746–51. doi:10.1074/jbc.272.32.19746. PMID 9242632.
Hiromasa Y, Fujisawa T, Aso Y, Roche TE (Feb 2004). "Organization of the cores of the mammalian pyruvate dehydrogenase complex formed by E2 and E2 plus the E3-binding protein and their capacities to bind the E1 and E3 components". The Journal of Biological Chemistry. 279 (8): 6921–33. doi:10.1074/jbc.M308172200. PMID 14638692.
Ciszak EM, Makal A, Hong YS, Vettaikkorumakankauv AK, Korotchkina LG, Patel MS (Jan 2006). "How dihydrolipoamide dehydrogenase-binding protein binds dihydrolipoamide dehydrogenase in the human pyruvate dehydrogenase complex". The Journal of Biological Chemistry. 281 (1): 648–55. doi:10.1074/jbc.M507850200. PMID 16263718.
Brautigam CA, Wynn RM, Chuang JL, Machius M, Tomchick DR, Chuang DT (Mar 2006). "Structural insight into interactions between dihydrolipoamide dehydrogenase (E3) and E3 binding protein of human pyruvate dehydrogenase complex". Structure. 14 (3): 611–21. doi:10.1016/j.str.2006.01.001. PMC 2879633. PMID 16442803.
Brown RM, Head RA, Morris AA, Raiman JA, Walter JH, Whitehouse WP, Brown GK (Sep 2006). "Pyruvate dehydrogenase E3 binding protein (protein X) deficiency". Developmental Medicine and Child Neurology. 48 (9): 756–60. doi:10.1017/S0012162206001617. PMID 16904023.
Ling M, McEachern G, Seyda A, MacKay N, Scherer SW, Bratinova S, Beatty B, Giovannucci-Uzielli ML, Robinson BH (Mar 1998). "Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiency". Human Molecular Genetics. 7 (3): 501–5. doi:10.1093/hmg/7.3.501. PMID 9467010.
Miné M, Brivet M, Schiff M, de Baulny HO, Chuzhanova N, Marsac C (2006). "A novel gross deletion caused by non-homologous recombination of the PDHX gene in a patient with pyruvate dehydrogenase deficiency". Molecular Genetics and Metabolism. 89 (1–2): 106–10. doi:10.1016/j.ymgme.2006.06.002. PMID 16843025.
Schiff M, Miné M, Brivet M, Marsac C, Elmaleh-Bergés M, Evrard P, Ogier de Baulny H (Apr 2006). "Leigh's disease due to a new mutation in the PDHX gene". Annals of Neurology. 59 (4): 709–14. doi:10.1002/ana.20818. PMID 16566017. S2CID 43132798.
McHugh A, Robe AJ, Palmer JM, Jones DE (May 2006). "PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis". Liver International. 26 (4): 406–13. doi:10.1111/j.1478-3231.2006.01253.x. PMID 16629643. S2CID 43447893.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000110435 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000010914 – Ensembl, May 2017

nih.gov

pubmed.ncbi.nlm.nih.gov

Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C (Dec 1997). "Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis". American Journal of Human Genetics. 61 (6): 1318–26. doi:10.1086/301653. PMC 1716072. PMID 9399911.
Ling M, McEachern G, Seyda A, MacKay N, Scherer SW, Bratinova S, Beatty B, Giovannucci-Uzielli ML, Robinson BH (Mar 1998). "Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiency". Human Molecular Genetics. 7 (3): 501–5. doi:10.1093/hmg/7.3.501. PMID 9467010.
Gawin B, Niederführ A, Schumacher N, Hummerich H, Little PF, Gessler M (Nov 1999). "A 7.5 Mb sequence-ready PAC contig and gene expression map of human chromosome 11p13-p14.1". Genome Research. 9 (11): 1074–86. doi:10.1101/gr.9.11.1074. PMC 310838. PMID 10568747.
Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C (Dec 1997). "Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis". American Journal of Human Genetics. 61 (6): 1318–26. doi:10.1086/301653. PMC 1716072. PMID 9399911.
Harris RA, Bowker-Kinley MM, Wu P, Jeng J, Popov KM (Aug 1997). "Dihydrolipoamide dehydrogenase-binding protein of the human pyruvate dehydrogenase complex. DNA-derived amino acid sequence, expression, and reconstitution of the pyruvate dehydrogenase complex". The Journal of Biological Chemistry. 272 (32): 19746–51. doi:10.1074/jbc.272.32.19746. PMID 9242632.
Hiromasa Y, Fujisawa T, Aso Y, Roche TE (Feb 2004). "Organization of the cores of the mammalian pyruvate dehydrogenase complex formed by E2 and E2 plus the E3-binding protein and their capacities to bind the E1 and E3 components". The Journal of Biological Chemistry. 279 (8): 6921–33. doi:10.1074/jbc.M308172200. PMID 14638692.
Ciszak EM, Makal A, Hong YS, Vettaikkorumakankauv AK, Korotchkina LG, Patel MS (Jan 2006). "How dihydrolipoamide dehydrogenase-binding protein binds dihydrolipoamide dehydrogenase in the human pyruvate dehydrogenase complex". The Journal of Biological Chemistry. 281 (1): 648–55. doi:10.1074/jbc.M507850200. PMID 16263718.
Brautigam CA, Wynn RM, Chuang JL, Machius M, Tomchick DR, Chuang DT (Mar 2006). "Structural insight into interactions between dihydrolipoamide dehydrogenase (E3) and E3 binding protein of human pyruvate dehydrogenase complex". Structure. 14 (3): 611–21. doi:10.1016/j.str.2006.01.001. PMC 2879633. PMID 16442803.
Brown RM, Head RA, Morris AA, Raiman JA, Walter JH, Whitehouse WP, Brown GK (Sep 2006). "Pyruvate dehydrogenase E3 binding protein (protein X) deficiency". Developmental Medicine and Child Neurology. 48 (9): 756–60. doi:10.1017/S0012162206001617. PMID 16904023.
Ling M, McEachern G, Seyda A, MacKay N, Scherer SW, Bratinova S, Beatty B, Giovannucci-Uzielli ML, Robinson BH (Mar 1998). "Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiency". Human Molecular Genetics. 7 (3): 501–5. doi:10.1093/hmg/7.3.501. PMID 9467010.
Miné M, Brivet M, Schiff M, de Baulny HO, Chuzhanova N, Marsac C (2006). "A novel gross deletion caused by non-homologous recombination of the PDHX gene in a patient with pyruvate dehydrogenase deficiency". Molecular Genetics and Metabolism. 89 (1–2): 106–10. doi:10.1016/j.ymgme.2006.06.002. PMID 16843025.
Schiff M, Miné M, Brivet M, Marsac C, Elmaleh-Bergés M, Evrard P, Ogier de Baulny H (Apr 2006). "Leigh's disease due to a new mutation in the PDHX gene". Annals of Neurology. 59 (4): 709–14. doi:10.1002/ana.20818. PMID 16566017. S2CID 43132798.
McHugh A, Robe AJ, Palmer JM, Jones DE (May 2006). "PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis". Liver International. 26 (4): 406–13. doi:10.1111/j.1478-3231.2006.01253.x. PMID 16629643. S2CID 43447893.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: pyruvate dehydrogenase complex".
Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C (Dec 1997). "Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis". American Journal of Human Genetics. 61 (6): 1318–26. doi:10.1086/301653. PMC 1716072. PMID 9399911.
Gawin B, Niederführ A, Schumacher N, Hummerich H, Little PF, Gessler M (Nov 1999). "A 7.5 Mb sequence-ready PAC contig and gene expression map of human chromosome 11p13-p14.1". Genome Research. 9 (11): 1074–86. doi:10.1101/gr.9.11.1074. PMC 310838. PMID 10568747.
Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C (Dec 1997). "Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis". American Journal of Human Genetics. 61 (6): 1318–26. doi:10.1086/301653. PMC 1716072. PMID 9399911.
Brautigam CA, Wynn RM, Chuang JL, Machius M, Tomchick DR, Chuang DT (Mar 2006). "Structural insight into interactions between dihydrolipoamide dehydrogenase (E3) and E3 binding protein of human pyruvate dehydrogenase complex". Structure. 14 (3): 611–21. doi:10.1016/j.str.2006.01.001. PMC 2879633. PMID 16442803.

semanticscholar.org

api.semanticscholar.org

Schiff M, Miné M, Brivet M, Marsac C, Elmaleh-Bergés M, Evrard P, Ogier de Baulny H (Apr 2006). "Leigh's disease due to a new mutation in the PDHX gene". Annals of Neurology. 59 (4): 709–14. doi:10.1002/ana.20818. PMID 16566017. S2CID 43132798.
McHugh A, Robe AJ, Palmer JM, Jones DE (May 2006). "PDC-E3BP is not a dominant T-cell autoantigen in primary biliary cirrhosis". Liver International. 26 (4): 406–13. doi:10.1111/j.1478-3231.2006.01253.x. PMID 16629643. S2CID 43447893.

wikipathways.org

The interactive pathway map can be edited at WikiPathways: "GlycolysisGluconeogenesis_WP534".