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Volumn 346, Issue 3, 2005, Pages 875-894

Evolutionary profiles derived from the QR factorization of multiple structural alignments gives an economy of information

Author keywords

Aminoacyl tRNA synthetase; Evolution; Non redundant set; OB fold; Protein structure profiles

Indexed keywords

PROTEIN;

EID: 13844266306     PISSN: 00222836     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmb.2004.11.053     Document Type: Article
Times cited : (48)

References (67)
  • 2
    • 0013776758 scopus 로고
    • Molecules as documents of evolutionary history
    • E. Zuckerkandl, and L. Pauling Molecules as documents of evolutionary history J. Theor. Biol. 8 1965 357 366
    • (1965) J. Theor. Biol. , vol.8 , pp. 357-366
    • Zuckerkandl, E.1    Pauling, L.2
  • 3
    • 0035527414 scopus 로고    scopus 로고
    • Environmental diversity of bacteria and archaea
    • E.F. DeLong, and N.R. Pace Environmental diversity of bacteria and archaea Syst. Biol. 50 2001 470 478
    • (2001) Syst. Biol. , vol.50 , pp. 470-478
    • Delong, E.F.1    Pace, N.R.2
  • 4
    • 0001271789 scopus 로고
    • Phylogenetic structure of the prokaryotic domain: The primary kingdoms
    • C.R. Woese, and G.E. Fox Phylogenetic structure of the prokaryotic domain: the primary kingdoms Proc. Natl Acad. Sci. USA 74 1977 5088 5090
    • (1977) Proc. Natl Acad. Sci. USA , vol.74 , pp. 5088-5090
    • Woese, C.R.1    Fox, G.E.2
  • 6
    • 0023084055 scopus 로고
    • Progressive sequence alignment as a prerequisite to correct phylogenetic trees
    • D.F. Feng, and R.F. Doolittle Progressive sequence alignment as a prerequisite to correct phylogenetic trees J. Mol. Evol. 25 1987 351 360
    • (1987) J. Mol. Evol. , vol.25 , pp. 351-360
    • Feng, D.F.1    Doolittle, R.F.2
  • 9
    • 0346494946 scopus 로고    scopus 로고
    • HOMSTRAD: Recent developments in the homologous protein structure alignment database
    • L.A. Stebbings, and K. Mizuguchi HOMSTRAD: recent developments in the homologous protein structure alignment database Nucl. Acids Res. 32 2004 D203 D207
    • (2004) Nucl. Acids Res. , vol.32
    • Stebbings, L.A.1    Mizuguchi, K.2
  • 11
    • 0030925920 scopus 로고    scopus 로고
    • Pfam: A comprehensive database of protein domain families based on seed alignments
    • E.L.L. Sonnhammer, S.R. Eddy, and R. Durbin Pfam: a comprehensive database of protein domain families based on seed alignments Proteins: Struct. Funct. Genet. 28 1997 405 420
    • (1997) Proteins: Struct. Funct. Genet. , vol.28 , pp. 405-420
    • Sonnhammer, E.L.L.1    Eddy, S.R.2    Durbin, R.3
  • 12
    • 0035783055 scopus 로고    scopus 로고
    • On the evolution of protein folds: Are similar motifs in different protein folds the result of convergence, insertion, or relics of an ancient peptide world?
    • A.N. Lupas, C.P. Ponting, and R.B. Russell On the evolution of protein folds: are similar motifs in different protein folds the result of convergence, insertion, or relics of an ancient peptide world? J. Struct. Biol. 134 2001 191 203
    • (2001) J. Struct. Biol. , vol.134 , pp. 191-203
    • Lupas, A.N.1    Ponting, C.P.2    Russell, R.B.3
  • 13
    • 0037423702 scopus 로고    scopus 로고
    • COMPASS: A tool for comparison of multiple protein alignments with assessment of statistical significance
    • R. Sadreyev, and N. Grishin COMPASS: a tool for comparison of multiple protein alignments with assessment of statistical significance J. Mol. Biol. 326 2003 317 336
    • (2003) J. Mol. Biol. , vol.326 , pp. 317-336
    • Sadreyev, R.1    Grishin, N.2
  • 14
    • 0344873345 scopus 로고    scopus 로고
    • On the role of structural information in remote homology detection and sequence alignment: New methods using hybrid sequence profiles
    • C.L. Tang, L. Xie, I.Y.Y. Koh, S. Posy, E. Alexov, and B. Honig On the role of structural information in remote homology detection and sequence alignment: new methods using hybrid sequence profiles J. Mol. Biol. 334 2003 1043 1062
    • (2003) J. Mol. Biol. , vol.334 , pp. 1043-1062
    • Tang, C.L.1    Xie, L.2    Koh, I.Y.Y.3    Posy, S.4    Alexov, E.5    Honig, B.6
  • 15
    • 2942619012 scopus 로고    scopus 로고
    • 3DCoffee: Combining protein sequences and structures within multiple sequence alignments
    • O. O'Sullivan, K. Suhre, C. Abergel, D.G. Higgins, and C. Notredame 3DCoffee: combining protein sequences and structures within multiple sequence alignments J. Mol. Biol. 340 2004 385 395
    • (2004) J. Mol. Biol. , vol.340 , pp. 385-395
    • O'Sullivan, O.1    Suhre, K.2    Abergel, C.3    Higgins, D.G.4    Notredame, C.5
  • 16
  • 17
    • 10744220076 scopus 로고    scopus 로고
    • Using multiple structure alignments, fast model building, and energetic analysis in fold recognition and homology modeling
    • D. Petrey, Z. Xiang, C.L. Tang, L. Xie, M. Gimpelev, T. Mitros, and C.S. Soto Using multiple structure alignments, fast model building, and energetic analysis in fold recognition and homology modeling Proteins: Struct. Funct. Genet. 53 2003 430 435
    • (2003) Proteins: Struct. Funct. Genet. , vol.53 , pp. 430-435
    • Petrey, D.1    Xiang, Z.2    Tang, C.L.3    Xie, L.4    Gimpelev, M.5    Mitros, T.6    Soto, C.S.7
  • 19
    • 0037423764 scopus 로고    scopus 로고
    • Functional fingerprints of folds: Evidence for correlated structure-function evolution
    • B.E. Shakhnovich, N.V. Dokholyan, C. DeLisi, and E.I. Shakhnovich Functional fingerprints of folds: evidence for correlated structure-function evolution J. Mol. Biol. 326 2003 1 9
    • (2003) J. Mol. Biol. , vol.326 , pp. 1-9
    • Shakhnovich, B.E.1    Dokholyan, N.V.2    Delisi, C.3    Shakhnovich, E.I.4
  • 21
    • 0036667733 scopus 로고    scopus 로고
    • Knowledge-based potential functions in protein design
    • W.P. Russ, and R. Ranganathan Knowledge-based potential functions in protein design Curr. Opin. Struct. Biol. 12 2002 447 452
    • (2002) Curr. Opin. Struct. Biol. , vol.12 , pp. 447-452
    • Russ, W.P.1    Ranganathan, R.2
  • 22
    • 0028946084 scopus 로고
    • Phylogenetic identification and in situ detection of individual microbial cells without cultivation
    • R.I. Amann, W. Ludwig, and K.H. Schleifer Phylogenetic identification and in situ detection of individual microbial cells without cultivation Microbiol. Rev. 59 1995 143 169
    • (1995) Microbiol. Rev. , vol.59 , pp. 143-169
    • Amann, R.I.1    Ludwig, W.2    Schleifer, K.H.3
  • 23
    • 0030982247 scopus 로고    scopus 로고
    • A molecular view of microbial diversity and the biosphere
    • N.R. Pace A molecular view of microbial diversity and the biosphere Science 276 1997 734 740
    • (1997) Science , vol.276 , pp. 734-740
    • Pace, N.R.1
  • 24
    • 1542377296 scopus 로고    scopus 로고
    • Community structure and metabolism through reconstruction of microbial genomes from the environment
    • G.W. Tyson, J. Chapman, P. Hugenholtz, E. Allen, R.J. Ram, and P.M. Richardson Community structure and metabolism through reconstruction of microbial genomes from the environment Nature 428 2004 37 43
    • (2004) Nature , vol.428 , pp. 37-43
    • Tyson, G.W.1    Chapman, J.2    Hugenholtz, P.3    Allen, E.4    Ram, R.J.5    Richardson, P.M.6
  • 26
    • 0031829372 scopus 로고    scopus 로고
    • Removing near-neighbour redundancy from large protein sequence collections
    • L. Holm, and C. Sander Removing near-neighbour redundancy from large protein sequence collections Bioinformatics 14 1998 423 429
    • (1998) Bioinformatics , vol.14 , pp. 423-429
    • Holm, L.1    Sander, C.2
  • 28
    • 0043180474 scopus 로고    scopus 로고
    • PISCES: A protein sequence culling server
    • G. Wang, and R.L. Dunbrack Jr PISCES: a protein sequence culling server Bioinformatics 19 2003 1589 1591
    • (2003) Bioinformatics , vol.19 , pp. 1589-1591
    • Wang, G.1    Dunbrack Jr., R.L.2
  • 29
    • 0033940118 scopus 로고    scopus 로고
    • RSDB: Representative protein sequence databases have high information content
    • J. Park, L. Holm, A. Heger, and C. Chothia RSDB: representative protein sequence databases have high information content Bioinformatics 16 2000 458 464
    • (2000) Bioinformatics , vol.16 , pp. 458-464
    • Park, J.1    Holm, L.2    Heger, A.3    Chothia, C.4
  • 30
    • 0024544755 scopus 로고
    • A fast and sensitive multiple sequence alignment algorithm
    • M. Vingron, and P. Argos A fast and sensitive multiple sequence alignment algorithm Comput. Appl. Biosci. 5 1989 115 121
    • (1989) Comput. Appl. Biosci. , vol.5 , pp. 115-121
    • Vingron, M.1    Argos, P.2
  • 31
    • 0028043552 scopus 로고
    • Position-based sequence weights
    • S. Heniko, and J.G. Heniko Position-based sequence weights J. Mol. Biol. 243 1994 574 578
    • (1994) J. Mol. Biol. , vol.243 , pp. 574-578
    • Heniko, S.1    Heniko, J.G.2
  • 32
    • 0034951509 scopus 로고    scopus 로고
    • Optimal classification of protein sequences and selection of representative sets from multiple alignments: Application to homologous families and lessons for structural genomics
    • A.C.W. May Optimal classification of protein sequences and selection of representative sets from multiple alignments: application to homologous families and lessons for structural genomics Protein Eng. 14 2001 209 217
    • (2001) Protein Eng. , vol.14 , pp. 209-217
    • May, A.C.W.1
  • 34
    • 0026743174 scopus 로고
    • Multiple protein sequence alignment from tertiary structure comparison: Assignment of global and residue confidence levels
    • R.B. Russell, and G.J. Barton Multiple protein sequence alignment from tertiary structure comparison: assignment of global and residue confidence levels Proteins: Struct. Funct. Genet. 14 1992 309 323
    • (1992) Proteins: Struct. Funct. Genet. , vol.14 , pp. 309-323
    • Russell, R.B.1    Barton, G.J.2
  • 36
    • 0035327183 scopus 로고    scopus 로고
    • Evaluating protein structure-prediction schemes using energy landscape theory, IBM
    • M.P. Eastwood, C. Hardin, Z. Luthey-Schulten, and P.G. Wolynes Evaluating protein structure-prediction schemes using energy landscape theory, IBM J. Res. Dev. 45 2001 475 497
    • (2001) J. Res. Dev. , vol.45 , pp. 475-497
    • Eastwood, M.P.1    Hardin, C.2    Luthey-Schulten, Z.3    Wolynes, P.G.4
  • 37
    • 0029895539 scopus 로고    scopus 로고
    • Self-consistently optimized statistical mechanical energy functions for sequence structure alignment
    • K. Koretke, Z. Luthey-Schulten, and P. Wolynes Self-consistently optimized statistical mechanical energy functions for sequence structure alignment Protein Sci. 5 1996 1043 1059
    • (1996) Protein Sci. , vol.5 , pp. 1043-1059
    • Koretke, K.1    Luthey-Schulten, Z.2    Wolynes, P.3
  • 39
    • 0000652188 scopus 로고
    • Unitary triangularization of a nonsymmetric matrix
    • A.S. Householder Unitary triangularization of a nonsymmetric matrix JACM 5 1958 339 342
    • (1958) JACM , vol.5 , pp. 339-342
    • Householder, A.S.1
  • 41
    • 0000924593 scopus 로고
    • Numerical methods for solving linear least squares problems
    • G. Golub Numerical methods for solving linear least squares problems Numer. Math. 7 1965 206 216
    • (1965) Numer. Math. , vol.7 , pp. 206-216
    • Golub, G.1
  • 43
    • 0242585484 scopus 로고    scopus 로고
    • A new family of global protein shape descriptors
    • P. Rogen, and H. Bohr A new family of global protein shape descriptors Math. Biosci. 182 2003 167 181
    • (2003) Math. Biosci. , vol.182 , pp. 167-181
    • Rogen, P.1    Bohr, H.2
  • 45
    • 0032120691 scopus 로고    scopus 로고
    • Transducer placement for broadband active vibration control using a novel multidimensional qr factorization
    • L.P. Heck, J.A. Olkin, and K. Naghshineh Transducer placement for broadband active vibration control using a novel multidimensional qr factorization J. Vib. Acoust. 120 1998 663 670
    • (1998) J. Vib. Acoust. , vol.120 , pp. 663-670
    • Heck, L.P.1    Olkin, J.A.2    Naghshineh, K.3
  • 46
    • 13844284979 scopus 로고    scopus 로고
    • Evolutionary profiles from the QR factorization of multiple sequence alignments
    • A. Sethi, P. O'Donoghue, and Z. Luthey-Schulten Evolutionary profiles from the QR factorization of multiple sequence alignments Proc. Natl Acad. Sci. USA 2005 in the press
    • (2005) Proc. Natl Acad. Sci. USA
    • Sethi, A.1    O'Donoghue, P.2    Luthey-Schulten, Z.3
  • 47
    • 0000122573 scopus 로고
    • PHYLIP-phylogeny inference package (version 3.2)
    • J. Felsenstein PHYLIP-phylogeny inference package (version 3.2) Cladistics 5 1989 164 166
    • (1989) Cladistics , vol.5 , pp. 164-166
    • Felsenstein, J.1
  • 48
    • 0000825481 scopus 로고
    • A statistical method for evaluating systematic relationships
    • R.R. Sokal, and C.D. Michener A statistical method for evaluating systematic relationships Univ. Kansas Sci. Bull. 28 1958 1409 1438
    • (1958) Univ. Kansas Sci. Bull. , vol.28 , pp. 1409-1438
    • Sokal, R.R.1    Michener, C.D.2
  • 49
    • 2342578493 scopus 로고
    • Molecular disease and evolution
    • L. Pauling Molecular disease and evolution Bull. NY Acad. Med. 40 1964 334 342
    • (1964) Bull. NY Acad. Med. , vol.40 , pp. 334-342
    • Pauling, L.1
  • 50
    • 0037173066 scopus 로고    scopus 로고
    • On the evolution of cells
    • C.R. Woese On the evolution of cells Proc. Natl Acad. Sci. USA 99 2002 8742 8747
    • (2002) Proc. Natl Acad. Sci. USA , vol.99 , pp. 8742-8747
    • Woese, C.R.1
  • 51
    • 0034053846 scopus 로고    scopus 로고
    • Aminoacyl-tRNA synthetases, the genetic code, and the evolutionary process
    • C.R. Woese, G. Olsen, M. Ibba, and D. Söll Aminoacyl-tRNA synthetases, the genetic code, and the evolutionary process Microbiol. Mol. Bio. Rev. 64 2000 202 236
    • (2000) Microbiol. Mol. Bio. Rev. , vol.64 , pp. 202-236
    • Woese, C.R.1    Olsen, G.2    Ibba, M.3    Söll, D.4
  • 53
    • 0022706389 scopus 로고
    • The relation between the divergence of sequence and structure in proteins
    • C. Chothia, and A.M. Lesk The relation between the divergence of sequence and structure in proteins EMBO J. 5 1986 823 826
    • (1986) EMBO J. , vol.5 , pp. 823-826
    • Chothia, C.1    Lesk, A.M.2
  • 54
    • 0036840353 scopus 로고    scopus 로고
    • Analysis of protein sequence/structure similarity relationships
    • H.H. Gan, R.A. Perlow, S. Roy, J. Ko, M. Wu, and J. Huang Analysis of protein sequence/structure similarity relationships Biophys. J. 83 2002 2781 2791
    • (2002) Biophys. J. , vol.83 , pp. 2781-2791
    • Gan, H.H.1    Perlow, R.A.2    Roy, S.3    Ko, J.4    Wu, M.5    Huang, J.6
  • 55
    • 0031915895 scopus 로고    scopus 로고
    • Universally conserved translation initiation factors
    • N.C. Kyrpides, and C.R. Woese Universally conserved translation initiation factors Proc. Natl Acad. Sci. USA 95 1998 224 228
    • (1998) Proc. Natl Acad. Sci. USA , vol.95 , pp. 224-228
    • Kyrpides, N.C.1    Woese, C.R.2
  • 56
    • 0032584201 scopus 로고    scopus 로고
    • Archaeal translation initiation revisited: The initiation factor 2 and eukaryotic initiation factor 2b alpha-beta-delta subunit families
    • N.C. Kyrpides, and C.R. Woese Archaeal translation initiation revisited: the initiation factor 2 and eukaryotic initiation factor 2b alpha-beta-delta subunit families Proc. Natl Acad. Sci. USA 95 1998 3726 3730
    • (1998) Proc. Natl Acad. Sci. USA , vol.95 , pp. 3726-3730
    • Kyrpides, N.C.1    Woese, C.R.2
  • 58
    • 0035910063 scopus 로고    scopus 로고
    • Combining multiple structure and sequence alignments to improve sequence detection and alignment: Application to the SH2 domains of Janus kinases
    • B. Al-Lazikani, F.B. Sheinerman, and B. Honig Combining multiple structure and sequence alignments to improve sequence detection and alignment: application to the SH2 domains of Janus kinases Proc. Natl Acad. Sci. USA 98 2001 14796 14801
    • (2001) Proc. Natl Acad. Sci. USA , vol.98 , pp. 14796-14801
    • Al-Lazikani, B.1    Sheinerman, F.B.2    Honig, B.3
  • 59
    • 0031743421 scopus 로고    scopus 로고
    • Profile hidden Markov models
    • S.R. Eddy Profile hidden Markov models Bioinformatics 14 1998 755 763
    • (1998) Bioinformatics , vol.14 , pp. 755-763
    • Eddy, S.R.1
  • 61
    • 0027178211 scopus 로고
    • Representing an ensemble of NMR-derived protein structures by a single structure
    • M.J. Sutcliffe Representing an ensemble of NMR-derived protein structures by a single structure Protein Sci. 2 1993 936 944
    • (1993) Protein Sci. , vol.2 , pp. 936-944
    • Sutcliffe, M.J.1
  • 63
    • 0029913807 scopus 로고    scopus 로고
    • An evolutionary trace method defines binding surfaces common to protein families
    • O. Lichtarge, H.R. Bourne, and F.E. Cohen An evolutionary trace method defines binding surfaces common to protein families J. Mol. Biol. 257 1996 342 358
    • (1996) J. Mol. Biol. , vol.257 , pp. 342-358
    • Lichtarge, O.1    Bourne, H.R.2    Cohen, F.E.3
  • 64
    • 2942547529 scopus 로고    scopus 로고
    • Using 3D hidden Markov models that explicitly represent spatial coordinates to model and compare protein structures
    • V. Alexandrov, and M. Gerstein Using 3D hidden Markov models that explicitly represent spatial coordinates to model and compare protein structures BMC Bioinformat. 5 2004 2
    • (2004) BMC Bioinformat. , vol.5 , pp. 2
    • Alexandrov, V.1    Gerstein, M.2
  • 65
    • 0028961335 scopus 로고
    • SCOP: A structural classification of proteins database for the investigation of sequences and structures
    • A.G. Murzin, S.E. Brenner, T. Hubbard, and C. Chothia SCOP: a structural classification of proteins database for the investigation of sequences and structures J. Mol. Biol. 247 1995 536 540
    • (1995) J. Mol. Biol. , vol.247 , pp. 536-540
    • Murzin, A.G.1    Brenner, S.E.2    Hubbard, T.3    Chothia, C.4
  • 67
    • 0037472710 scopus 로고    scopus 로고
    • Solution structure of a tmRNA-binding protein, SmpB, from Thermus thermophilus
    • T. Someya, N. Nameki, H. Hosoi, S. Suzuki, H. Hatanaka, and M. Fujii Solution structure of a tmRNA-binding protein, SmpB, from Thermus thermophilus FEBS Letters 535 2003 94 100
    • (2003) FEBS Letters , vol.535 , pp. 94-100
    • Someya, T.1    Nameki, N.2    Hosoi, H.3    Suzuki, S.4    Hatanaka, H.5    Fujii, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.