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Volumn 5, Issue 12, 2009, Pages

Trade-off between positive and negative design of protein stability: From lattice models to real proteins

Author keywords

[No Author keywords available]

Indexed keywords

CONFORMATIONS; CRYSTAL LATTICES; ECONOMIC AND SOCIAL EFFECTS;

EID: 74549184107     PISSN: 1553734X     EISSN: 15537358     Source Type: Journal    
DOI: 10.1371/journal.pcbi.1000592     Document Type: Article
Times cited : (32)

References (36)
  • 1
    • 0025040232 scopus 로고
    • De novo design, expression, and characterization of Felix: A four-helix bundle protein of native-like sequence
    • Hecht MH, Richardson JS, Richardson DC, Ogden RC (1990) De novo design, expression, and characterization of Felix: a four-helix bundle protein of native-like sequence. Science 249: 884-891.
    • (1990) Science , vol.249 , pp. 884-891
    • Hecht, M.H.1    Richardson, J.S.2    Richardson, D.C.3    Ogden, R.C.4
  • 2
    • 0030886443 scopus 로고    scopus 로고
    • Rational protein design: Combining theory and experiment
    • Hellinga HW (1997) Rational protein design: Combining theory and experiment. Proc Natl Acad Sci USA 94: 10015-10017.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 10015-10017
    • Hellinga, H.W.1
  • 3
    • 34047232678 scopus 로고    scopus 로고
    • Positive and negative design in stability and thermal adaptation of natural proteins
    • Berezovsky IN, Zeldovich KB, Shakhnovich EI (2007) Positive and negative design in stability and thermal adaptation of natural proteins. PLoS Comput Biol 3: 498-507.
    • (2007) PLoS Comput Biol , vol.3 , pp. 498-507
    • Berezovsky, I.N.1    Zeldovich, K.B.2    Shakhnovich, E.I.3
  • 4
    • 0032502839 scopus 로고    scopus 로고
    • Contact order, transition state placement and the refolding rates of single domain proteins
    • Plaxco KW, Simons KT, Baker D (1998) Contact order, transition state placement and the refolding rates of single domain proteins. J Mol Biol 277: 985-994.
    • (1998) J Mol Biol , vol.277 , pp. 985-994
    • Plaxco, K.W.1    Simons, K.T.2    Baker, D.3
  • 5
    • 0028929556 scopus 로고
    • Principles of protein folding-a perspective from simple exact models
    • Dill KA, Bromberg S, Yue K, Fiebig KM, Yee DP, et al. (1995) Principles of protein folding-a perspective from simple exact models. Protein Sci 4: 561-602.
    • (1995) Protein Sci , vol.4 , pp. 561-602
    • Dill, K.A.1    Bromberg, S.2    Yue, K.3    Fiebig, K.M.4    Yee, D.P.5
  • 7
  • 8
    • 0030604696 scopus 로고    scopus 로고
    • Local interactions dominate folding in a simple protein model
    • Unger R, Moult J (1996) Local interactions dominate folding in a simple protein model. J Mol Biol 259: 988-994.
    • (1996) J Mol Biol , vol.259 , pp. 988-994
    • Unger, R.1    Moult, J.2
  • 9
    • 0013527261 scopus 로고    scopus 로고
    • Perspectives on protein evolution from simple exact models
    • Chan HS, Bornberg-Bauer E (2002) Perspectives on protein evolution from simple exact models. Appl Bioinformatics 1: 121-144.
    • (2002) Appl Bioinformatics , vol.1 , pp. 121-144
    • Chan, H.S.1    Bornberg-Bauer, E.2
  • 10
    • 1842839788 scopus 로고    scopus 로고
    • Simulating protein evolution in sequence and structure space
    • Xia Y, Levitt M (2004) Simulating protein evolution in sequence and structure space. Curr Opin Struct Biol 14: 202-207.
    • (2004) Curr Opin Struct Biol , vol.14 , pp. 202-207
    • Xia, Y.1    Levitt, M.2
  • 11
    • 43949093427 scopus 로고    scopus 로고
    • Understanding protein evolution: From protein physics to Darwinian selection
    • Zeldovich KB, Shakhnovich EI (2008) Understanding protein evolution: from protein physics to Darwinian selection. Annu Rev Phys Chem 59: 105-127.
    • (2008) Annu Rev Phys Chem , vol.59 , pp. 105-127
    • Zeldovich, K.B.1    Shakhnovich, E.I.2
  • 12
    • 0030322783 scopus 로고    scopus 로고
    • Double-mutant cycles: A powerful tool for analysing protein structure and function
    • Horovitz A (1996) Double-mutant cycles: a powerful tool for analysing protein structure and function. Fold & Des 1: R121-R126.
    • (1996) Fold & Des , vol.1
    • Horovitz, A.1
  • 13
    • 65249121395 scopus 로고    scopus 로고
    • Analysing the origin of long-range interactions in proteins using lattice models
    • Noivirt-Brik O, Unger R, Horovitz A (2009) Analysing the origin of long-range interactions in proteins using lattice models. BMC Struct Biol 9: 4.
    • (2009) BMC Struct Biol , vol.9 , pp. 4
    • Noivirt-Brik, O.1    Unger, R.2    Horovitz, A.3
  • 14
    • 36549094651 scopus 로고
    • Intrachain loops in polymers: Effects of excluded volume
    • Chan HS, Dill KA (1989) Intrachain loops in polymers: effects of excluded volume. J Chem Phys 90: 492-509.
    • (1989) J Chem Phys , vol.90 , pp. 492-509
    • Chan, H.S.1    Dill, K.A.2
  • 16
    • 0028125904 scopus 로고
    • How frequent are correlated changes in families of protein sequences?
    • Neher E (1994) How frequent are correlated changes in families of protein sequences? Proc Natl Acad Sci USA 91: 98-102.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 98-102
    • Neher, E.1
  • 17
    • 0033536602 scopus 로고    scopus 로고
    • Evolutionarily conserved pathways of energetic connectivity in protein families
    • Lockless SW, Ranganathan R (1999) Evolutionarily conserved pathways of energetic connectivity in protein families. Science 286: 295-299.
    • (1999) Science , vol.286 , pp. 295-299
    • Lockless, S.W.1    Ranganathan, R.2
  • 18
    • 0036721218 scopus 로고    scopus 로고
    • Mapping pathways of allosteric communication in GroEL by analysis of correlated mutations
    • Kass I, Horovitz A (2002) Mapping pathways of allosteric communication in GroEL by analysis of correlated mutations. Proteins: Struct Funct Genet 48: 611-617.
    • (2002) Proteins: Struct Funct Genet , vol.48 , pp. 611-617
    • Kass, I.1    Horovitz, A.2
  • 19
    • 0036568319 scopus 로고    scopus 로고
    • In silico two-hybrid system for the selection of physically interacting protein pairs
    • Pazos F, Valencia A (2002) In silico two-hybrid system for the selection of physically interacting protein pairs. Proteins: Struct Funct Genet 47: 219-227.
    • (2002) Proteins: Struct Funct Genet , vol.47 , pp. 219-227
    • Pazos, F.1    Valencia, A.2
  • 20
    • 58549114185 scopus 로고    scopus 로고
    • Identification of direct residue contacts in protein-protein interaction by message passing
    • Weigt M, White RA, Szurmant H, Hoch JA, Hwa T (2009) Identification of direct residue contacts in protein-protein interaction by message passing. Proc Natl Acad Sci USA 106: 67-72.
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 67-72
    • Weigt, M.1    White, R.A.2    Szurmant, H.3    Hoch, J.A.4    Hwa, T.5
  • 21
  • 22
    • 0034724418 scopus 로고    scopus 로고
    • Separation of phylogenetic and functional associations in biological sequences by using the parametric bootstrap
    • Wollenberg KR, Atchley WR (2000) Separation of phylogenetic and functional associations in biological sequences by using the parametric bootstrap. Proc Natl Acad Sci USA 97: 3288-3291.
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 3288-3291
    • Wollenberg, K.R.1    Atchley, W.R.2
  • 23
    • 3042842115 scopus 로고    scopus 로고
    • Influence of conservation on calculations of amino acid covariance in multiple sequence alignments
    • Fodor AA, Aldrich RW (2004) Influence of conservation on calculations of amino acid covariance in multiple sequence alignments. Proteins: Struct Funct Bioinf 56: 211-221.
    • (2004) Proteins: Struct Funct Bioinf , vol.56 , pp. 211-221
    • Fodor, A.A.1    Aldrich, R.W.2
  • 24
    • 20844452182 scopus 로고    scopus 로고
    • Detection and reduction of evolutionary noise in correlated mutation analysis
    • Noivirt O, Eisenstein M, Horovitz A (2005) Detection and reduction of evolutionary noise in correlated mutation analysis. Protein Eng Des Sel 18: 247-253.
    • (2005) Protein Eng Des Sel , vol.18 , pp. 247-253
    • Noivirt, O.1    Eisenstein, M.2    Horovitz, A.3
  • 25
    • 22744447508 scopus 로고    scopus 로고
    • Proteome-wide analysis of chaperonin-dependent protein folding in Escherichia coli
    • Kerner MJ, Naylor DJ, Ishihama Y, Maier T, Chang HC, et al. (2005) Proteome-wide analysis of chaperonin-dependent protein folding in Escherichia coli. Cell 122: 209-220.
    • (2005) Cell , vol.122 , pp. 209-220
    • Kerner, M.J.1    Naylor, D.J.2    Ishihama, Y.3    Maier, T.4    Chang, H.C.5
  • 26
    • 24644472817 scopus 로고    scopus 로고
    • Physics and evolution of thermophilic adaptation
    • Berezovsky IN, Shakhnovich EI (2005) Physics and evolution of thermophilic adaptation. Proc Natl Acad Sci USA 102: 12742-12747.
    • (2005) Proc Natl Acad Sci USA , vol.102 , pp. 12742-12747
    • Berezovsky, I.N.1    Shakhnovich, E.I.2
  • 27
    • 37349101689 scopus 로고    scopus 로고
    • Gaining and losing the thermophilic adaptation in prokaryotes
    • Puigbò P, Pasamontes A, Garcia-Vallve S (2007) Gaining and losing the thermophilic adaptation in prokaryotes. Trends Genet 24: 10-14.
    • (2007) Trends Genet , vol.24 , pp. 10-14
    • Puigbò, P.1    Pasamontes, A.2    Garcia-Vallve, S.3
  • 28
    • 48349109787 scopus 로고    scopus 로고
    • How does gene expression level contribute to thermophilic adaptation of prokaryotes? An exploration based on predictors
    • Wang J, Ma BG, Zhang HY, Chen LL, Zhang SC (2008) How does gene expression level contribute to thermophilic adaptation of prokaryotes? An exploration based on predictors. Gene 421: 32-36.
    • (2008) Gene , vol.421 , pp. 32-36
    • Wang, J.1    Ma, B.G.2    Zhang, H.Y.3    Chen, L.L.4    Zhang, S.C.5
  • 31
    • 0025093185 scopus 로고
    • Estimating the contribution of engineered surface electrostatic interactions to protein stability by using double-mutant cycles
    • Serrano L, Horovitz A, Avron B, Bycroft M, Fersht AR (1990) Estimating the contribution of engineered surface electrostatic interactions to protein stability by using double-mutant cycles. Biochemistry 29: 9343-9352.
    • (1990) Biochemistry , vol.29 , pp. 9343-9352
    • Serrano, L.1    Horovitz, A.2    Avron, B.3    Bycroft, M.4    Fersht, A.R.5
  • 36
    • 0027968068 scopus 로고
    • CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
    • Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22: 4673-4680.
    • (1994) Nucleic Acids Res , vol.22 , pp. 4673-4680
    • Thompson, J.D.1    Higgins, D.G.2    Gibson, T.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.