Protein disorder - a breakthrough invention of evolution?

被引:113
作者
Schlessinger, Avner [4 ,5 ]
Schaefer, Christian
Vicedo, Esmeralda
Schmidberger, Markus
Punta, Marco [1 ,2 ]
Rost, Burkhard [1 ,2 ,3 ]
机构
[1] TUM, Inst Adv Study, D-85748 Garching, Germany
[2] TUM Bioinformat, New York Consortium Membrane Prot Struct NYCOMPS, D-85748 Garching, Germany
[3] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[4] Univ Calif San Francisco, Dept Pharmaceut Chem, Dept Bioengn & Therapeut Sci, San Francisco, CA USA
[5] Univ Calif San Francisco, Calif Inst Quantitat Biosci, San Francisco, CA 94143 USA
关键词
INTRINSICALLY UNSTRUCTURED PROTEINS; STRUCTURAL GENOMICS; SECONDARY STRUCTURE; FLEXIBLE NETS; AMINO-ACID; PREDICTION; SEQUENCE; DATABASE; ANNOTATION; INSIGHTS;
D O I
10.1016/j.sbi.2011.03.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As an operational definition, we refer to regions in proteins that do not adopt regular three-dimensional structures in isolation, as disordered regions. An antipode to disorder would be 'well-structured' rather than 'ordered'. Here, we argue for the following three hypotheses. Firstly, it is more useful to picture disorder as a distinct phenomenon in structural biology than as an extreme example of protein flexibility. Secondly, there are many very different flavors of protein disorder, nevertheless, it seems advantageous to portray the universe of all possible proteins in terms of two main types: well-structured, disordered. There might be a third type 'other' but we have so far no positive evidence for this. Thirdly, nature uses protein disorder as a tool to adapt to different environments. Protein disorder is evolutionarily conserved and this maintenance of disorder is highly nontrivial. Increasingly integrating protein disorder into the toolbox of a living cell was a crucial step in the evolution from simple bacteria to complex eukaryotes. We need new advanced computational methods to study this new milestone in the advance of protein biology.
引用
收藏
页码:412 / 418
页数:7
相关论文
共 81 条
[21]   Benchmarking homology detection procedures with low complexity filters [J].
Forslund, Kristoffer ;
Sonnhammer, Erik L. L. .
BIOINFORMATICS, 2009, 25 (19) :2500-2505
[22]   Unique amino acid composition of proteins in halophilic bacteria [J].
Fukuchi, S ;
Yoshimune, K ;
Wakayama, M ;
Moriguchi, M ;
Nishikawa, K .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 327 (02) :347-357
[23]   Local structural disorder imparts plasticity on linear motifs [J].
Fuxreiter, Monika ;
Tompa, Peter ;
Simon, Istvan .
BIOINFORMATICS, 2007, 23 (08) :950-956
[24]   Regulation of cell division by intrinsically unstructured proteins: Intrinsic flexibility, modularity, and signaling conduits [J].
Galea, Charles A. ;
Wang, Yuefeng ;
Sivakolundu, Sivashankar G. ;
Kriwacki, Richard W. .
BIOCHEMISTRY, 2008, 47 (29) :7598-7609
[25]   Large-Scale Analysis of Thermostable, Mammalian Proteins Provides Insights into the Intrinsically Disordered Proteome [J].
Galea, Charles A. ;
High, Anthony A. ;
Obenauer, John C. ;
Mishra, Ashutosh ;
Park, Cheon-Gil ;
Punta, Marco ;
Schllessinger, Avner ;
Ma, Jing ;
Rost, Burkhard ;
Slaughter, Clive A. ;
Kriwacki, Richard W. .
JOURNAL OF PROTEOME RESEARCH, 2009, 8 (01) :211-226
[26]   A structural census of the current population of protein sequences [J].
Gerstein, M ;
Levitt, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (22) :11911-11916
[27]   The rules of disorder or why disorder rules [J].
Gsponer, Joerg ;
Babu, M. Madan .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2009, 99 (2-3) :94-103
[28]   Verification of alternative splicing variants based on domain integrity, truncation length and intrinsic protein disorder [J].
Hegyi, Hedi ;
Kalmar, Lajos ;
Horvath, Tamas ;
Tompa, Peter .
NUCLEIC ACIDS RESEARCH, 2011, 39 (04) :1208-1219
[29]   Globally, unrelated protein sequences appear random [J].
Lavelle, Daniel T. ;
Pearson, William R. .
BIOINFORMATICS, 2010, 26 (03) :310-318
[30]  
LESK AM, 1991, PROTEIN ARCHITECTURE, V1