메뉴 건너뛰기




Volumn 1140, Issue , 2014, Pages 27-34

Structural genomics of human proteins

Author keywords

Human membrane protein; Human proteins; Methyltransferases; Protein families; Protein kinases; Structural basis of disease

Indexed keywords

PROTEIN;

EID: 84907924958     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4939-0354-2_2     Document Type: Article
Times cited : (3)

References (38)
  • 3
    • 0037032835 scopus 로고    scopus 로고
    • The protein kinase complement of the human genome. Science (New York
    • Manning G, Whyte DB, Martinez R, Hunter T, Sudarsanam S (2002) The protein kinase complement of the human genome. Science (New York, NY) 298:1912–1934
    • (2002) NY) , vol.298 , pp. 1912-1934
    • Manning, G.1    Whyte, D.B.2    Martinez, R.3    Hunter, T.4    Sudarsanam, S.5
  • 6
    • 67650437045 scopus 로고    scopus 로고
    • Large-scale structural biology of the human proteome
    • Edwards A (2009) Large-scale structural biology of the human proteome. Annu Rev Biochem 78:541–568
    • (2009) Annu Rev Biochem , vol.78 , pp. 541-568
    • Edwards, A.1
  • 7
    • 0022977712 scopus 로고
    • A noncatalytic domain conserved among cytoplasmic protein-tyrosine kinases modifies the kinase function and transforming activity ofFujinami sarcoma virus P130gag-fps
    • Sadowski I, Stone JC, Pawson T (1986) A noncatalytic domain conserved among cytoplasmic protein-tyrosine kinases modifies the kinase function and transforming activity ofFujinami sarcoma virus P130gag-fps. Mol Cell Biol 6:4396–4408
    • (1986) Mol Cell Biol , vol.6 , pp. 4396-4408
    • Sadowski, I.1    Stone, J.C.2    Pawson, T.3
  • 8
    • 0021173703 scopus 로고
    • Identification of functional regions in the transforming protein of Fujinami sarcoma virus by in-phase insertion mutagenesis
    • Stone JC, Atkinson T, Smith M, Pawson T (1984) Identification of functional regions in the transforming protein of Fujinami sarcoma virus by in-phase insertion mutagenesis. Cell 37:549–558
    • (1984) Cell , vol.37 , pp. 549-558
    • Stone, J.C.1    Atkinson, T.2    Smith, M.3    Pawson, T.4
  • 14
    • 54449100397 scopus 로고    scopus 로고
    • Evidence that two enzyme-derived histidine ligands are sufficient for iron binding and catalysis by factor inhibiting HIF (FIH)
    • Hewitson KS, Holmes SL, Ehrismann D, Hardy AP, Chowdhury R, Schofield CJ, McDonough MA (2008) Evidence that two enzyme-derived histidine ligands are sufficient for iron binding and catalysis by factor inhibiting HIF (FIH). J Biol Chem 283:25971–25978
    • (2008) J Biol Chem , vol.283 , pp. 25971-25978
    • Hewitson, K.S.1    Holmes, S.L.2    Ehrismann, D.3    Hardy, A.P.4    Chowdhury, R.5    Schofield, C.J.6    McDonough, M.A.7
  • 24
    • 22244450719 scopus 로고    scopus 로고
    • Protein families and their evolution-a structural perspective
    • Orengo CA, Thornton JM (2005) Protein families and their evolution-a structural perspective. Annu Rev Biochem 74:867–900
    • (2005) Annu Rev Biochem , vol.74 , pp. 867-900
    • Orengo, C.A.1    Thornton, J.M.2
  • 27
    • 84874865318 scopus 로고    scopus 로고
    • Next generation sequencing in cancer research and clinical application
    • Shyr D, Liu Q (2013) Next generation sequencing in cancer research and clinical application. Biol Proced Online 15:4
    • (2013) Biol Proced Online , vol.15 , pp. 4
    • Shyr, D.1    Liu, Q.2
  • 29
    • 84867252179 scopus 로고    scopus 로고
    • An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect
    • Janer A, Antonicka H, Lalonde E, Nishimura T, Sasarman F, Brown GK, Brown RM, Majewski J, Shoubridge EA (2012) An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect. Am J Hum Genet 91:737–743
    • (2012) Am J Hum Genet , vol.91 , pp. 737-743
    • Janer, A.1    Antonicka, H.2    Lalonde, E.3    Nishimura, T.4    Sasarman, F.5    Brown, G.K.6    Brown, R.M.7    Majewski, J.8    Shoubridge, E.A.9
  • 34
    • 84863970074 scopus 로고    scopus 로고
    • De novo mutations in human genetic disease
    • Veltman JA, Brunner HG (2012) De novo mutations in human genetic disease. Nat Rev Genet 13:565–575
    • (2012) Nat Rev Genet , vol.13 , pp. 565-575
    • Veltman, J.A.1    Brunner, H.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.