Discovering co-occurring patterns and their biological significance in protein families
暂无分享,去创建一个
Andrew K. C. Wong | En-Shiun Annie Lee | Ho-Yin Sze-To | Sanderz Fung | A. Wong | E. Lee | Ho-Yin Sze-To | Sanderz Fung
[1] Photon Factory,et al. Ubiquitin-binding domains — from structures to functions , 2009 .
[2] S J Ferguson,et al. Still a puzzle: why is haem covalently attached in c-type cytochromes? , 1999, Structure.
[3] T. N. Bhat,et al. The Protein Data Bank , 2000, Nucleic Acids Res..
[4] L. Holm,et al. The Pfam protein families database , 2005, Nucleic Acids Res..
[5] I Clark-Lewis,et al. A rationale for the absolute conservation of Asn70 and Pro71 in mitochondrial cytochromes c suggested by protein engineering. , 1997, Biochemistry.
[6] Radford M. Neal. Pattern Recognition and Machine Learning , 2007, Technometrics.
[7] Asimul Islam,et al. The role of key residues in structure, function, and stability of cytochrome-c , 2013, Cellular and Molecular Life Sciences.
[8] F. Cohen,et al. An evolutionary trace method defines binding surfaces common to protein families. , 1996, Journal of molecular biology.
[9] R. Dickerson,et al. Redox conformation changes in refined tuna cytochrome c. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[10] C. Wallace,et al. Probing the role of the conserved beta-II turn Pro-76/Gly-77 of mitochondrial cytochrome c. , 2007, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[11] Ulrike von Luxburg,et al. A tutorial on spectral clustering , 2007, Stat. Comput..
[12] Emad Tajkhorshid,et al. The binding interface of cytochrome c and cytochrome c₁ in the bc₁ complex: rationalizing the role of key residues. , 2010, Biophysical journal.
[13] B. Chait,et al. Substitutions engineered by chemical synthesis at three conserved sites in mitochondrial cytochrome c. Thermodynamic and functional consequences. , 1989, The Journal of biological chemistry.
[14] E. Margoliash,et al. The low ionic strength crystal structure of horse cytochrome c at 2.1 A resolution and comparison with its high ionic strength counterpart. , 1995, Structure.
[15] G J Pielak,et al. Exploring the interface between the N- and C-terminal helices of cytochrome c by random mutagenesis within the C-terminal helix. , 1993, Biochemistry.
[16] O. Lichtarge,et al. Evolutionary Trace of G Protein-coupled Receptors Reveals Clusters of Residues That Determine Global and Class-specific Functions* , 2004, Journal of Biological Chemistry.
[17] E Margoliash,et al. Effects of mutating Asn-52 to isoleucine on the haem-linked properties of cytochrome c. , 1994, The Biochemical journal.
[18] Kara L Bren,et al. The chemistry and biochemistry of heme c: functional bases for covalent attachment. , 2008, Natural product reports.
[19] E. Birney,et al. Pfam: the protein families database , 2013, Nucleic Acids Res..
[20] T. Hwa,et al. Identification of direct residue contacts in protein–protein interaction by message passing , 2009, Proceedings of the National Academy of Sciences.
[21] C. Bugg,et al. Comparison of the three-dimensional structures of human, yeast, and oat ubiquitin. , 1987, The Journal of biological chemistry.
[22] T. Alleyne,et al. Probing the specifics of substrate binding for cytochrome c oxidase: a computer assisted approach. , 2009, The West Indian medical journal.
[23] Sigurd M. Wilbanks,et al. Conformational change and human cytochrome c function: mutation of residue 41 modulates caspase activation and destabilizes Met-80 coordination , 2013, JBIC Journal of Biological Inorganic Chemistry.
[24] Vipin Kumar,et al. Introduction to Data Mining , 2022, Data Mining and Machine Learning Applications.
[25] D. Higgins,et al. T-Coffee: A novel method for fast and accurate multiple sequence alignment. , 2000, Journal of molecular biology.
[26] Conrad C. Huang,et al. UCSF Chimera—A visualization system for exploratory research and analysis , 2004, J. Comput. Chem..
[27] Pauline Mayonove,et al. The alpha helix of ubiquitin interacts with yeast cyclin-dependent kinase subunit CKS1. , 2007, Biochemistry.
[28] Andrew K. C. Wong,et al. Confirming biological significance of co-occurrence clusters of aligned pattern clusters , 2013, 2013 IEEE International Conference on Bioinformatics and Biomedicine.
[29] Olivier Poch,et al. A Comprehensive Benchmark Study of Multiple Sequence Alignment Methods: Current Challenges and Future Perspectives , 2011, PloS one.
[30] Andrew K. C. Wong,et al. Discovery of Delta Closed Patterns and Noninduced Patterns from Sequences , 2012, IEEE Transactions on Knowledge and Data Engineering.
[31] Soichi Wakatsuki,et al. Ubiquitin-binding domains — from structures to functions , 2009, Nature Reviews Molecular Cell Biology.
[32] S. Hagen,et al. Rapid intrachain binding of histidine-26 and histidine-33 to heme in unfolded ferrocytochrome C. , 2002, Biochemistry.
[33] G J Pielak,et al. Role of phenylalanine-82 in yeast iso-1-cytochrome c and remote conformational changes induced by a serine residue at this position. , 1988, Biochemistry.
[34] María Martín,et al. Activities at the Universal Protein Resource (UniProt) , 2013, Nucleic Acids Res..
[35] C. Sander,et al. Direct-coupling analysis of residue coevolution captures native contacts across many protein families , 2011, Proceedings of the National Academy of Sciences.
[36] A. Haas,et al. Site-directed mutagenesis of ubiquitin. Differential roles for arginine in the interaction with ubiquitin-activating enzyme. , 1994, Biochemistry.
[37] Anil K. Jain. Data clustering: 50 years beyond K-means , 2008, Pattern Recognit. Lett..
[38] Xuhua Xia,et al. Position Weight Matrix, Gibbs Sampler, and the Associated Significance Tests in Motif Characterization and Prediction , 2012, Scientifica.
[39] Erik van Nimwegen,et al. Disentangling Direct from Indirect Co-Evolution of Residues in Protein Alignments , 2010, PLoS Comput. Biol..
[40] J. Thompson,et al. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.
[41] R. Dickerson,et al. Conformation change of cytochrome c. I. Ferrocytochrome c structure refined at 1.5 A resolution. , 1981, Journal of molecular biology.
[42] Tao Jiang,et al. On the Complexity of Multiple Sequence Alignment , 1994, J. Comput. Biol..
[43] K D Wilkinson,et al. Three-dimensional structure of ubiquitin at 2.8 A resolution. , 1985, Proceedings of the National Academy of Sciences of the United States of America.