TY - JOUR
T1 - TMSNP
T2 - A web server to predict pathogenesis of missense mutations in the transmembrane region of membrane proteins
AU - Garcia-Recio, Adrián
AU - Gómez-Tamayo, José Carlos
AU - Reina, Iker
AU - Campillo, Mercedes
AU - Cordomí, Arnau
AU - Olivella, Mireia
N1 - Publisher Copyright:
© 2021 The Author(s).
PY - 2021/3/1
Y1 - 2021/3/1
N2 - The massive amount of data generated from genome sequencing brings tons of newly identified mutations, whose pathogenic/non-pathogenic effects need to be evaluated. This has given rise to several mutation predictor tools that, in general, do not consider the specificities of the various protein groups. We aimed to develop a predictor tool dedicated to membrane proteins, under the premise that their specific structural features and environment would give different responses to mutations compared to globular proteins. For this purpose, we created TMSNP, a database that currently contains information from 2624 pathogenic and 196 705 non-pathogenic reported mutations located in the transmembrane region of membrane proteins. By computing various conservation parameters on these mutations in combination with annotations, we trained a machine-learning model able to classify mutations as pathogenic or not. TMSNP (freely available at http://lmc.uab.es/tmsnp/) improves considerably the prediction power of commonly used mutation predictors trained with globular proteins.
AB - The massive amount of data generated from genome sequencing brings tons of newly identified mutations, whose pathogenic/non-pathogenic effects need to be evaluated. This has given rise to several mutation predictor tools that, in general, do not consider the specificities of the various protein groups. We aimed to develop a predictor tool dedicated to membrane proteins, under the premise that their specific structural features and environment would give different responses to mutations compared to globular proteins. For this purpose, we created TMSNP, a database that currently contains information from 2624 pathogenic and 196 705 non-pathogenic reported mutations located in the transmembrane region of membrane proteins. By computing various conservation parameters on these mutations in combination with annotations, we trained a machine-learning model able to classify mutations as pathogenic or not. TMSNP (freely available at http://lmc.uab.es/tmsnp/) improves considerably the prediction power of commonly used mutation predictors trained with globular proteins.
UR - http://www.scopus.com/inward/record.url?scp=85122965306&partnerID=8YFLogxK
U2 - 10.1093/nargab/lqab008
DO - 10.1093/nargab/lqab008
M3 - Article
C2 - 33655207
AN - SCOPUS:85122965306
SN - 2631-9268
VL - 3
JO - NAR Genomics and Bioinformatics
JF - NAR Genomics and Bioinformatics
IS - 1
M1 - lqab008
ER -