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Bioinformatic Prediction of Gene Ontology Terms of Uncharacterized Proteins from Chromosome 11.
Hwang, Heeyoun; Im, Ji Eun; Yang, Yeji; Kim, Hyejin; Kwon, Kyung-Hoon; Kim, Yun-Hee; Kim, Jin Young; Yoo, Jong Shin.
Afiliação
  • Hwang H; Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.
  • Im JE; Division of Convergence Technology, Research Institute of National Cancer Center, Goyang 10408, Republic of Korea.
  • Yang Y; Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.
  • Kim H; Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.
  • Kwon KH; Graduate School of Analytical Science and Technology, Chungnam National University, Daejeon 34134, Republic of Korea.
  • Kim YH; Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.
  • Kim JY; Division of Convergence Technology, Research Institute of National Cancer Center, Goyang 10408, Republic of Korea.
  • Yoo JS; Department of Cancer Biomedical Science, The National Cancer Center Graduate School of Cancer Science and Policy, Goyang 10408, Republic of Korea.
J Proteome Res ; 19(12): 4907-4912, 2020 12 04.
Article em En | MEDLINE | ID: mdl-33089979
In chromosome 11, 71 out of its 1254 proteins remain functionally uncharacterized on the basis of their existence evidence (uPE1s) following the latest version of neXtProt (release 2020-01-17). Because in vivo and in vitro experimental strategies are often time-consuming and labor-intensive, there is a need for a bioinformatics tool to predict the function annotation. Here, we used I-TASSER/COFACTOR provided on the neXtProt web site, which predicts gene ontology (GO) terms based on the 3D structure of the protein. I-TASSER/COFACTOR predicted 2413 GO terms with a benchmark dataset of the 22 proteins belonging to PE1 of chromosome 11. In this study, we developed a filtering algorithm in order to select specific GO terms using the GO map generated by I-TASSER/COFACTOR. As a result, 187 specific GO terms showed a higher average precision-recall score at the least cellular component term compared to 2413 predicted GO terms. Next, we applied 65 proteins belonging to uPE1s of chromosome 11, and then 409 out of 6684 GO terms survived, where 103 and 142 GO terms of molecular function and biological process, respectively, were included. Representatively, the cellular component GO terms of CCDC90B, C11orf52, and the SMAP were predicted and validated using the overexpression system into 293T cells and immunofluorescence staining. We will further study their biological and molecular functions toward the goal of the neXt-CP50 project as a part of C-HPP. We shared all results and programs in Github (https://github.com/heeyounh/I-TASSER-COFACTOR-filtering.git).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 11 / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 11 / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article