A copy of this work was available on the public web and has been preserved in the Wayback Machine. The capture dates from 2019; you can also visit the original URL.
The file type is application/pdf
.
Structural fragment clustering reveals novel structural and functional motifs in α-helical transmembrane proteins
2010
BMC Bioinformatics
A large proportion of an organism's genome encodes for membrane proteins. Membrane proteins are important for many cellular processes, and several diseases can be linked to mutations in them. With the tremendous growth of sequence data, there is an increasing need to reliably identify membrane proteins from sequence, to functionally annotate them, and to correctly predict their topology. Results: We introduce a technique called structural fragment clustering, which learns sequential motifs from
doi:10.1186/1471-2105-11-204
pmid:20420672
pmcid:PMC2876129
fatcat:r7xhbks42naqpbv76boa55w2pq