Flavors of protein disorder.

@article{citeulike:768199, abstract = {Intrinsically disordered proteins are characterized by long regions lacking 3-D structure in their native states, yet they have been so far associated with 28 distinguishable functions. Previous studies showed that protein predictors trained on disorder from one type of protein often achieve poor accuracy on disorder of proteins of a different type, thus indicating significant differences in sequence properties among disordered proteins. Important biological problems are identifying different types, or flavors, of disorder and examining their relationships with protein function. Innovative use of computational methods is needed in addressing these problems due to relative scarcity of experimental data and background knowledge related to protein disorder. We developed an algorithm that partitions protein disorder into flavors based on competition among increasing numbers of predictors, with prediction accuracy determining both the number of distinct predictors and the partitioning of the individual proteins. Using 145 variously characterized proteins with long (>30 amino acids) disordered regions, 3 flavors, called V, C, and S, were identified by this approach, with the V subset containing 52 segments and 7743 residues, C containing 39 segments and 3402 residues, and S containing 54 segments and 5752 residues. The V, C, and S flavors were distinguishable by amino acid compositions, sequence locations, and biological function. For the sequences in SwissProt and 28 genomes, their protein functions exhibit correlations with the commonness and usage of different disorder flavors, suggesting different flavor-function sets across these protein groups. Overall, the results herein support the flavor-function approach as a useful complement to structural genomics as a means for automatically assigning possible functions to sequences.}, address = {Center for Information Science and Technology, Temple University, Philadelphia, Pennsylvania 19122, USA.}, author = {Vucetic, S. and Brown, C. J. and Dunker, A. K. and Obradovic, Z. }, citeulike-article-id = {768199}, doi = {http://dx.doi.org/10.1002/prot.10437}, issn = {1097-0134}, journal = {Proteins}, keywords = {usa}, month = {September}, number = {4}, pages = {573--584}, posted-at = {2008-05-11 17:51:29}, priority = {2}, title = {Flavors of protein disorder.}, url = {http://dx.doi.org/10.1002/prot.10437}, volume = {52}, year = {2003} }

TY - JOUR ID - citeulike:768199 L3 - citeulike-article-id:768199 TI - Flavors of protein disorder. JF - Proteins VL - 52 IS - 4 SP - 573 EP - 584 AD - Center for Information Science and Technology, Temple University, Philadelphia, Pennsylvania 19122, USA. SN - 1097-0134 N2 - Intrinsically disordered proteins are characterized by long regions lacking 3-D structure in their native states, yet they have been so far associated with 28 distinguishable functions. Previous studies showed that protein predictors trained on disorder from one type of protein often achieve poor accuracy on disorder of proteins of a different type, thus indicating significant differences in sequence properties among disordered proteins. Important biological problems are identifying different types, or flavors, of disorder and examining their relationships with protein function. Innovative use of computational methods is needed in addressing these problems due to relative scarcity of experimental data and background knowledge related to protein disorder. We developed an algorithm that partitions protein disorder into flavors based on competition among increasing numbers of predictors, with prediction accuracy determining both the number of distinct predictors and the partitioning of the individual proteins. Using 145 variously characterized proteins with long (>30 amino acids) disordered regions, 3 flavors, called V, C, and S, were identified by this approach, with the V subset containing 52 segments and 7743 residues, C containing 39 segments and 3402 residues, and S containing 54 segments and 5752 residues. The V, C, and S flavors were distinguishable by amino acid compositions, sequence locations, and biological function. For the sequences in SwissProt and 28 genomes, their protein functions exhibit correlations with the commonness and usage of different disorder flavors, suggesting different flavor-function sets across these protein groups. Overall, the results herein support the flavor-function approach as a useful complement to structural genomics as a means for automatically assigning possible functions to sequences. KW - usa AU - Vucetic, S AU - Brown, CJ AU - Dunker, AK AU - Obradovic, Z PY - 2003/09/01/ UR - http://dx.doi.org/10.1002/prot.10437 ER -