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10.1073/pnas.1801182115

http://scihub22266oqcxt.onion/10.1073/pnas.1801182115
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C6042118!6042118 !29895692
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suck abstract from ncbi


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pmid29895692
      Proc+Natl+Acad+Sci+U+S+A 2018 ; 115 (26 ): 6703-6708
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  • Unique function words characterize genomic proteins #MMPMID29895692
  • Scaiewicz A ; Levitt M
  • Proc Natl Acad Sci U S A 2018[Jun]; 115 (26 ): 6703-6708 PMID29895692 show ga
  • Between 2009 and 2016 the number of protein sequences from known species increased 10-fold from 8 million to 85 million. About 80% of these sequences contain at least one region recognized by the conserved domain architecture retrieval tool (CDART) as a sequence motif. Motifs provide clues to biological function but CDART often matches the same region of a protein by two or more profiles. Such synonyms complicate estimates of functional complexity. We do full-linkage clustering of redundant profiles by finding maximum disjoint cliques: Each cluster is replaced by a single representative profile to give what we term a unique function word (UFW). From 2009 to 2016, the number of sequence profiles used by CDART increased by 80%; the number of UFWs increased more slowly by 30%, indicating that the number of UFWs may be saturating. The number of sequences matched by a single UFW (sequences with single domain architectures) increased as slowly as the number of different words, whereas the number of sequences matched by a combination of two or more UFWs in sequences with multiple domain architectures (MDAs) increased at the same rate as the total number of sequences. This combinatorial arrangement of a limited number of UFWs in MDAs accounts for the genomic diversity of protein sequences. Although eukaryotes and prokaryotes use very similar sets of "words" or UFWs (57% shared), the "sentences" (MDAs) are different (1.3% shared).
  • |*Conserved Sequence [MESH]
  • |*Genomics [MESH]
  • |*Protein Domains [MESH]
  • |*Software [MESH]
  • |Algorithms [MESH]
  • |Amino Acid Sequence [MESH]
  • |Cluster Analysis [MESH]
  • |Databases, Factual [MESH]
  • |Humans [MESH]
  • |Sequence Alignment [MESH]
  • |Sequence Homology, Amino Acid [MESH]


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