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Volumn 11, Issue 7, 2010, Pages 562-572

Predicting the melting point of human C-type lysozyme mutants

Author keywords

Distance constraint model; Heat capacity; Lysozyme; Melting point; Mutation; Protein stability

Indexed keywords

LYSOZYME; LYSOZYME TYPE C; UNCLASSIFIED DRUG;

EID: 79251478002     PISSN: 13892037     EISSN: None     Source Type: Journal    
DOI: 10.2174/138920310794109210     Document Type: Article
Times cited : (14)

References (45)
  • 1
    • 33846396137 scopus 로고    scopus 로고
    • Prediction of protein mutant stability using classification and regression tool
    • Huang, L.T.; Saraboji, K.; Ho, S.Y.; Hwang, S.F.; Ponnuswamy, M.N.; Gromiha, M.M. Prediction of protein mutant stability using classification and regression tool. Biophys. Chem., 2007, 125(2-3), 462-470.
    • (2007) Biophys. Chem , vol.125 , Issue.2-3 , pp. 462-470
    • Huang, L.T.1    Saraboji, K.2    Ho, S.Y.3    Hwang, S.F.4    Ponnuswamy, M.N.5    Gromiha, M.M.6
  • 2
    • 34447096122 scopus 로고    scopus 로고
    • Sequence analysis and rule development of predicting protein stability change upon mutation using decision tree model
    • Huang, L.T.; Gromiha, M.M.; Ho, S.Y. Sequence analysis and rule development of predicting protein stability change upon mutation using decision tree model. J. Mol. Model, 2007, 13(8), 879-890.
    • (2007) J. Mol. Model , vol.13 , Issue.8 , pp. 879-890
    • Huang, L.T.1    Gromiha, M.M.2    Ho, S.Y.3
  • 3
    • 34447338865 scopus 로고    scopus 로고
    • iPTREE-STAB, interpretable decision tree based method for predicting protein stability changes upon mutations
    • Huang, L.T.; Gromiha, M.M.; Ho, S.Y. iPTREE-STAB, interpretable decision tree based method for predicting protein stability changes upon mutations. Bioinformatics, 2007, 23(10), 1292-1293.
    • (2007) Bioinformatics , vol.23 , Issue.10 , pp. 1292-1293
    • Huang, L.T.1    Gromiha, M.M.2    Ho, S.Y.3
  • 4
    • 33644847172 scopus 로고    scopus 로고
    • Prediction of protein stability changes for single-site mutations using support vector machines
    • Cheng, J.; Randall, A.; Baldi, P. Prediction of protein stability changes for single-site mutations using support vector machines. Proteins, 2006, 62(4), 1125-1132.
    • (2006) Proteins , vol.62 , Issue.4 , pp. 1125-1132
    • Cheng, J.1    Randall, A.2    Baldi, P.3
  • 5
    • 27544469800 scopus 로고    scopus 로고
    • Predicting protein stability changes from sequences using support vector machines
    • Capriotti, E.; Fariselli, P.; Calabrese, R.; Casadio, R. Predicting protein stability changes from sequences using support vector machines. Bioinformatics, 2005, 21 Suppl 2, ii54-58.
    • (2005) Bioinformatics , vol.21 , Issue.SUPPL. 2
    • Capriotti, E.1    Fariselli, P.2    Calabrese, R.3    Casadio, R.4
  • 6
    • 23144461249 scopus 로고    scopus 로고
    • I-Mutant2.0, predicting stability changes upon mutation from the protein sequence or structure
    • Capriotti, E.; Fariselli, P.; Casadio, R. I-Mutant2.0, predicting stability changes upon mutation from the protein sequence or structure. Nucleic Acids Res., 2005, 33(Web Server issue), W306-310.
    • (2005) Nucleic Acids Res , vol.33 , Issue.Web Server issue
    • Capriotti, E.1    Fariselli, P.2    Casadio, R.3
  • 7
    • 0028300741 scopus 로고
    • Combining evolutionary information and neural networks to predict protein secondary structure
    • Rost, B.; Sander, C. Combining evolutionary information and neural networks to predict protein secondary structure. Proteins, 1994, 19(1), 55-72.
    • (1994) Proteins , vol.19 , Issue.1 , pp. 55-72
    • Rost, B.1    Sander, C.2
  • 8
    • 33745380521 scopus 로고    scopus 로고
    • Amino Acid Sequence Autocorrelation vectors and ensembles of Bayesian-Regularized Genetic Neural Networks for prediction of conformational stability of human lysozyme mutants
    • Caballero, J.; Fernandez, L.; Abreu, J.I.; Fernandez, M. Amino Acid Sequence Autocorrelation vectors and ensembles of Bayesian-Regularized Genetic Neural Networks for prediction of conformational stability of human lysozyme mutants. J. Chem. Inf. Model, 2006, 46(3), 1255-1268.
    • (2006) J. Chem. Inf. Model , vol.46 , Issue.3 , pp. 1255-1268
    • Caballero, J.1    Fernandez, L.2    Abreu, J.I.3    Fernandez, M.4
  • 9
    • 11844281294 scopus 로고    scopus 로고
    • A neural-network-based method for predicting protein stability changes upon single point mutations
    • Capriotti, E.; Fariselli, P.; Casadio, R. A neural-network-based method for predicting protein stability changes upon single point mutations. Bioinformatics, 2004, 20(Suppl 1), i63-68.
    • (2004) Bioinformatics , vol.20 , Issue.SUPPL. 1
    • Capriotti, E.1    Fariselli, P.2    Casadio, R.3
  • 10
    • 0024412497 scopus 로고
    • Mutational effects on protein stability
    • Alber, T. Mutational effects on protein stability. Annu. Rev. Biochem., 1989, 58, 765-798.
    • (1989) Annu. Rev. Biochem , vol.58 , pp. 765-798
    • Alber, T.1
  • 12
    • 0037432563 scopus 로고    scopus 로고
    • Contribution of surface salt bridges to protein stability, guidelines for protein engineering
    • Makhatadze, G.I.; Loladze, V.V.; Ermolenko, D.N.; Chen, X.; Thomas, S.T. Contribution of surface salt bridges to protein stability, guidelines for protein engineering. J. Mol. Biol., 2003, 327(5), 1135-1148.
    • (2003) J. Mol. Biol , vol.327 , Issue.5 , pp. 1135-1148
    • Makhatadze, G.I.1    Loladze, V.V.2    Ermolenko, D.N.3    Chen, X.4    Thomas, S.T.5
  • 13
    • 1042298814 scopus 로고    scopus 로고
    • Mechanism of thermostabilization in a designed cold shock protein with optimized surface electrostatic interactions
    • Makhatadze, G.I.; Loladze, V.V.; Gribenko, A.V.; Lopez, M.M. Mechanism of thermostabilization in a designed cold shock protein with optimized surface electrostatic interactions. J. Mol. Biol., 2004, 336(4), 929-942.
    • (2004) J. Mol. Biol , vol.336 , Issue.4 , pp. 929-942
    • Makhatadze, G.I.1    Loladze, V.V.2    Gribenko, A.V.3    Lopez, M.M.4
  • 14
    • 0242385395 scopus 로고    scopus 로고
    • Conferring thermostability to mesophilic proteins through optimized electrostatic surfaces
    • Torrez, M.; Schultehenrich, M.; Livesay, D.R. Conferring thermostability to mesophilic proteins through optimized electrostatic surfaces. Biophys. J., 2003, 85(5), 2845-2853.
    • (2003) Biophys. J , vol.85 , Issue.5 , pp. 2845-2853
    • Torrez, M.1    Schultehenrich, M.2    Livesay, D.R.3
  • 15
    • 0038650855 scopus 로고    scopus 로고
    • Comparison of calculation and experiment implicates significant electrostatic contributions to the binding stability of barnase and barstar
    • Dong, F.; Vijayakumar, M.; Zhou, H.X. Comparison of calculation and experiment implicates significant electrostatic contributions to the binding stability of barnase and barstar. Biophys. J., 2003, 85(1), 49-60.
    • (2003) Biophys. J , vol.85 , Issue.1 , pp. 49-60
    • Dong, F.1    Vijayakumar, M.2    Zhou, H.X.3
  • 16
    • 0037380834 scopus 로고    scopus 로고
    • Electrostatic contributions to the stability of a thermophilic cold shock protein
    • Zhou, H.X.; Dong, F. Electrostatic contributions to the stability of a thermophilic cold shock protein. Biophys. J., 2003, 84(4), 2216-2222.
    • (2003) Biophys. J , vol.84 , Issue.4 , pp. 2216-2222
    • Zhou, H.X.1    Dong, F.2
  • 17
    • 0036708444 scopus 로고    scopus 로고
    • Electrostatic contributions to T4 lysozyme stability, solvent-exposed charges versus semi-buried salt bridges
    • Dong, F.; Zhou, H.X. Electrostatic contributions to T4 lysozyme stability, solvent-exposed charges versus semi-buried salt bridges. Biophys. J., 2002, 83(3), 1341-1347.
    • (2002) Biophys. J , vol.83 , Issue.3 , pp. 1341-1347
    • Dong, F.1    Zhou, H.X.2
  • 18
    • 21244483843 scopus 로고    scopus 로고
    • Elucidating protein thermodynamics from the three-dimensional structure of the native state using network rigidity
    • Jacobs, D.J.; Dallakyan, S. Elucidating protein thermodynamics from the three-dimensional structure of the native state using network rigidity. Biophys. J., 2005, 88(2), 903-915.
    • (2005) Biophys. J , vol.88 , Issue.2 , pp. 903-915
    • Jacobs, D.J.1    Dallakyan, S.2
  • 19
    • 6344223617 scopus 로고    scopus 로고
    • A flexible approach for understanding protein stability
    • Livesay, D.R.; Dallakyan, S.; Wood, G.G.; Jacobs, D.J. A flexible approach for understanding protein stability. FEBS Lett., 2004, 576(3), 468-476.
    • (2004) FEBS Lett , vol.576 , Issue.3 , pp. 468-476
    • Livesay, D.R.1    Dallakyan, S.2    Wood, G.G.3    Jacobs, D.J.4
  • 20
    • 33745726737 scopus 로고    scopus 로고
    • Lessons in stability from thermophilic proteins
    • Razvi, A.; Scholtz, J.M. Lessons in stability from thermophilic proteins. Protein Sci., 2006, 15(7), 1569-1578.
    • (2006) Protein Sci , vol.15 , Issue.7 , pp. 1569-1578
    • Razvi, A.1    Scholtz, J.M.2
  • 21
    • 34147133371 scopus 로고    scopus 로고
    • Recent developments in methodologies for calculating the entropy and free energy of biological systems by computer simulation
    • Meirovitch, H. Recent developments in methodologies for calculating the entropy and free energy of biological systems by computer simulation. Curr. Opin. Struct. Biol., 2007, 17(2), 181-186.
    • (2007) Curr. Opin. Struct. Biol , vol.17 , Issue.2 , pp. 181-186
    • Meirovitch, H.1
  • 22
    • 0031022887 scopus 로고    scopus 로고
    • Additivity principles in biochemistry
    • Dill, K.A. Additivity principles in biochemistry. J. Biol. Chem., 1997, 272(2), 701-704.
    • (1997) J. Biol. Chem , vol.272 , Issue.2 , pp. 701-704
    • Dill, K.A.1
  • 23
    • 0028334097 scopus 로고
    • Decomposition of the free energy of a system in terms of specific interactions. Implications for theoretical and experimental studies
    • Mark, A.E.; van Gunsteren, W.F. Decomposition of the free energy of a system in terms of specific interactions. Implications for theoretical and experimental studies. J. Mol. Biol., 1994, 240(2), 167-176.
    • (1994) J. Mol. Biol , vol.240 , Issue.2 , pp. 167-176
    • Mark, A.E.1    van Gunsteren, W.F.2
  • 24
    • 1542285840 scopus 로고    scopus 로고
    • Network rigidity at finite temperature, relationships between thermodynamic stability, the nonadditivity of entropy, and cooperativity in molecular systems
    • Jacobs, D.J.; Dallakyan, S.; Wood, G.G.; Heckathorne, A. Network rigidity at finite temperature, relationships between thermodynamic stability, the nonadditivity of entropy, and cooperativity in molecular systems. Phys. Rev. E. Stat. Nonlin. Soft Matter Phys., 2003, 68(6 Pt 1), 061109.
    • (2003) Phys. Rev. E. Stat. Nonlin. Soft Matter Phys , vol.68 , Issue.6 PART 1 , pp. 061109
    • Jacobs, D.J.1    Dallakyan, S.2    Wood, G.G.3    Heckathorne, A.4
  • 25
    • 0035427398 scopus 로고    scopus 로고
    • Protein flexibility predictions using graph theory
    • Jacobs, D.J.; Rader, A.J.; Kuhn, L.A.; Thorpe, M.F. Protein flexibility predictions using graph theory. Proteins, 2001, 44(2), 150-165.
    • (2001) Proteins , vol.44 , Issue.2 , pp. 150-165
    • Jacobs, D.J.1    Rader, A.J.2    Kuhn, L.A.3    Thorpe, M.F.4
  • 26
    • 0000785338 scopus 로고
    • Generic rigidity percolation, The pebble game
    • Jacobs, D.J.; Thorpe, M.F. Generic rigidity percolation, The pebble game. Phys. Rev. Lett., 1995, 75(22), 4051-4054.
    • (1995) Phys. Rev. Lett , vol.75 , Issue.22 , pp. 4051-4054
    • Jacobs, D.J.1    Thorpe, M.F.2
  • 27
    • 72549119922 scopus 로고    scopus 로고
    • Helix/coil nucleation, a local response to global demands
    • Vorov, O.K.; Livesay, D.R.; Jacobs, D.J. Helix/coil nucleation, a local response to global demands. Biophys. J., 2009, 97(11), 3000-3009.
    • (2009) Biophys. J , vol.97 , Issue.11 , pp. 3000-3009
    • Vorov, O.K.1    Livesay, D.R.2    Jacobs, D.J.3
  • 28
    • 0343742614 scopus 로고    scopus 로고
    • Automated design of the surface positions of protein helices
    • Dahiyat, B.I.; Gordon, D.B.; Mayo, S.L. Automated design of the surface positions of protein helices. Protein Sci., 1997, 6(6), 1333-1337.
    • (1997) Protein Sci , vol.6 , Issue.6 , pp. 1333-1337
    • Dahiyat, B.I.1    Gordon, D.B.2    Mayo, S.L.3
  • 29
    • 0037432188 scopus 로고    scopus 로고
    • Protein folding, could hydrophobic collapse be coupled with hydrogen-bond formation?
    • Fernandez, A.; Kardos, J.; Goto, Y. Protein folding, could hydrophobic collapse be coupled with hydrogen-bond formation? FEBS Lett., 2003, 536(1-3), 187-192.
    • (2003) FEBS Lett , vol.536 , Issue.1-3 , pp. 187-192
    • Fernandez, A.1    Kardos, J.2    Goto, Y.3
  • 30
    • 30344476409 scopus 로고    scopus 로고
    • Conserved quantitative stability/flexibility relationships (QSFR) in an orthologous RNase H pair
    • Livesay, D.R.; Jacobs, D.J. Conserved quantitative stability/flexibility relationships (QSFR) in an orthologous RNase H pair. Proteins, 2006, 62(1), 130-143.
    • (2006) Proteins , vol.62 , Issue.1 , pp. 130-143
    • Livesay, D.R.1    Jacobs, D.J.2
  • 31
    • 33646033429 scopus 로고    scopus 로고
    • Elucidating quantitative stability/flexibility relationships within thioredoxin and its fragments using a distance constraint model
    • Jacobs, D.J.; Livesay, D.R.; Hules, J.; Tasayco, M.L. Elucidating quantitative stability/flexibility relationships within thioredoxin and its fragments using a distance constraint model. J. Mol. Biol., 2006, 358(3), 882-904.
    • (2006) J. Mol. Biol , vol.358 , Issue.3 , pp. 882-904
    • Jacobs, D.J.1    Livesay, D.R.2    Hules, J.3    Tasayco, M.L.4
  • 32
    • 51749092455 scopus 로고    scopus 로고
    • Hydrogen bond networks determine emergent mechanical and thermodynamic properties across a protein family
    • Livesay, D.R.; Huynh, D.H.; Dallakyan, S.; Jacobs, D.J. Hydrogen bond networks determine emergent mechanical and thermodynamic properties across a protein family. Chem. Cent. J., 2008, 2, 17.
    • (2008) Chem. Cent. J , vol.2 , pp. 17
    • Livesay, D.R.1    Huynh, D.H.2    Dallakyan, S.3    Jacobs, D.J.4
  • 33
    • 66149154705 scopus 로고    scopus 로고
    • Unifying mechanical and thermodynamic descriptions across the thioredoxin protein family
    • Mottonen, J.M.; Xu, M.; Jacobs, D.J.; Livesay, D.R. Unifying mechanical and thermodynamic descriptions across the thioredoxin protein family. Proteins, 2009, 75(3), 610-627.
    • (2009) Proteins , vol.75 , Issue.3 , pp. 610-627
    • Mottonen, J.M.1    Xu, M.2    Jacobs, D.J.3    Livesay, D.R.4
  • 34
    • 0032581023 scopus 로고    scopus 로고
    • Contribution of hydrogen bonds to the conformational stability of human lysozyme, calorimetry and X-ray analysis of six tyrosine → phenylalanine mutants
    • Yamagata, Y.; Kubota, M.; Sumikawa, Y.; Funahashi, J.; Takano, K.; Fujii, S.; Yutani, K. Contribution of hydrogen bonds to the conformational stability of human lysozyme, calorimetry and X-ray analysis of six tyrosine → phenylalanine mutants. Biochemistry, 1998, 37(26), 9355-9362.
    • (1998) Biochemistry , vol.37 , Issue.26 , pp. 9355-9362
    • Yamagata, Y.1    Kubota, M.2    Sumikawa, Y.3    Funahashi, J.4    Takano, K.5    Fujii, S.6    Yutani, K.7
  • 35
    • 0031050618 scopus 로고    scopus 로고
    • Contribution of the hydrophobic effect to the stability of human lysozyme, calorimetric studies and X-ray structural analyses of the nine valine to alanine mutants
    • Takano, K.; Yamagata, Y.; Fujii, S.; Yutani, K. Contribution of the hydrophobic effect to the stability of human lysozyme, calorimetric studies and X-ray structural analyses of the nine valine to alanine mutants. Biochemistry, 1997, 36(4), 688-698.
    • (1997) Biochemistry , vol.36 , Issue.4 , pp. 688-698
    • Takano, K.1    Yamagata, Y.2    Fujii, S.3    Yutani, K.4
  • 36
    • 0032834649 scopus 로고    scopus 로고
    • Experimental verification of the 'stability profile of mutant protein' (SPMP) data using mutant human lysozymes
    • Takano, K.; Ota, M.; Ogasahara, K.; Yamagata, Y.; Nishikawa, K.; Yutani, K. Experimental verification of the 'stability profile of mutant protein' (SPMP) data using mutant human lysozymes. Protein Eng., 1999, 12(8), 663-672.
    • (1999) Protein Eng , vol.12 , Issue.8 , pp. 663-672
    • Takano, K.1    Ota, M.2    Ogasahara, K.3    Yamagata, Y.4    Nishikawa, K.5    Yutani, K.6
  • 37
    • 0033485411 scopus 로고    scopus 로고
    • Effect of foreign N-terminal residues on the conformational stability of human lysozyme
    • Takano, K.; Tsuchimori, K.; Yamagata, Y.; Yutani, K. Effect of foreign N-terminal residues on the conformational stability of human lysozyme. Eur. J. Biochem., 1999, 266(2), 675-682.
    • (1999) Eur. J. Biochem , vol.266 , Issue.2 , pp. 675-682
    • Takano, K.1    Tsuchimori, K.2    Yamagata, Y.3    Yutani, K.4
  • 38
    • 0032744714 scopus 로고    scopus 로고
    • Contribution of amino acid substitutions at two different interior positions to the conformational stability of human lysozyme
    • Funahashi, J.; Takano, K.; Yamagata, Y.; Yutani, K. Contribution of amino acid substitutions at two different interior positions to the conformational stability of human lysozyme. Protein Eng., 1999, 12(10), 841-850.
    • (1999) Protein Eng , vol.12 , Issue.10 , pp. 841-850
    • Funahashi, J.1    Takano, K.2    Yamagata, Y.3    Yutani, K.4
  • 39
    • 0030474922 scopus 로고    scopus 로고
    • The structure, stability, and folding process of amyloidogenic mutant human lysozyme
    • Funahashi, J.; Takano, K.; Ogasahara, K.; Yamagata, Y.; Yutani, K. The structure, stability, and folding process of amyloidogenic mutant human lysozyme. J. Biochem., 1996, 120(6), 1216-1223.
    • (1996) J. Biochem , vol.120 , Issue.6 , pp. 1216-1223
    • Funahashi, J.1    Takano, K.2    Ogasahara, K.3    Yamagata, Y.4    Yutani, K.5
  • 40
    • 0026714968 scopus 로고
    • Role of proline residues in human lysozyme stability, a scanning calorimetric study combined with X-ray structure analysis of proline mutants
    • Herning, T.; Yutani, K.; Inaka, K.; Kuroki, R.; Matsushima, M.; Kikuchi, M. Role of proline residues in human lysozyme stability, a scanning calorimetric study combined with X-ray structure analysis of proline mutants. Biochemistry, 1992, 31(31), 7077-7085.
    • (1992) Biochemistry , vol.31 , Issue.31 , pp. 7077-7085
    • Herning, T.1    Yutani, K.2    Inaka, K.3    Kuroki, R.4    Matsushima, M.5    Kikuchi, M.6
  • 41
    • 0000159569 scopus 로고    scopus 로고
    • Protein structure and the energetics of protein stability
    • Robertson, A.D.; Murphy, K.P. Protein structure and the energetics of protein stability. Chem. Rev., 1997, 97(5), 1251-1268.
    • (1997) Chem. Rev , vol.97 , Issue.5 , pp. 1251-1268
    • Robertson, A.D.1    Murphy, K.P.2
  • 42
    • 23144457576 scopus 로고    scopus 로고
    • H++, a server for estimating pKas and adding missing hydrogens to macromolecules
    • Gordon, J.C.; Myers, J.B.; Folta, T.; Shoja, V.; Heath, L.S.; Onufriev, A. H++, a server for estimating pKas and adding missing hydrogens to macromolecules. Nucleic Acids Res., 2005, 33(Web Server issue), W368-371.
    • (2005) Nucleic Acids Res , vol.33 , Issue.Web Server issue
    • Gordon, J.C.1    Myers, J.B.2    Folta, T.3    Shoja, V.4    Heath, L.S.5    Onufriev, A.6
  • 43
    • 0029114703 scopus 로고
    • The heat capacity of proteins
    • Gomez, J.; Hilser, V.J.; Xie, D.; Freire, E. The heat capacity of proteins. Proteins, 1995, 22(4), 404-412.
    • (1995) Proteins , vol.22 , Issue.4 , pp. 404-412
    • Gomez, J.1    Hilser, V.J.2    Xie, D.3    Freire, E.4
  • 44
    • 0030059689 scopus 로고    scopus 로고
    • Forces contributing to the conformational stability of proteins
    • Pace, C.N.; Shirley, B.A.; McNutt, M.; Gajiwala, K. Forces contributing to the conformational stability of proteins. FASEB J., 1996, 10(1), 75-83.
    • (1996) FASEB J , vol.10 , Issue.1 , pp. 75-83
    • Pace, C.N.1    Shirley, B.A.2    McNutt, M.3    Gajiwala, K.4
  • 45
    • 0036291145 scopus 로고    scopus 로고
    • Predicting changes in the stability of proteins and protein complexes, a study of more than 1000 mutations
    • Guerois, R.; Nielsen, J.E.; Serrano, L. Predicting changes in the stability of proteins and protein complexes, a study of more than 1000 mutations. J. Mol. Biol., 2002, 320(2), 369-387.
    • (2002) J. Mol. Biol , vol.320 , Issue.2 , pp. 369-387
    • Guerois, R.1    Nielsen, J.E.2    Serrano, L.3


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