iMethyl-PseAAC: Identification of Protein Methylation Sites via a Pseudo Amino Acid Composition Approach
Year: 2014
Type: article
Abstract: Before becoming the native proteins during the biosynthesis, their polypeptide chains created by ribosome's translating mRNA will undergo a series of "product-forming" steps, such as cutting, folding, and posttranslational modification (PTM). Knowledge of PTMs in proteins is crucial for dynamic proteome analysis of various human diseases and epigenetic inheritance. One of the most important PTMs is the Arg- or Lys-methylation that occurs on arginine or lysine, respectively. Given a protein, which site of its Arg (or Lys) can be methylated, and which site cannot? This is the first important problem for understanding the methylation mechanism and drug development in depth. With the avalanche of protein sequences generated in the postgenomic age, its urgency has become self-evident. To address this problem, we proposed a new predictor, called iMethyl-PseAAC. In the prediction system, a peptide sample was formulated by a 346-dimensional vector, formed by incorporating its physicochemical, sequence evolution, biochemical, and structural disorder information into the general form of pseudo amino acid composition. It was observed by the rigorous jackknife test and independent dataset test that iMethyl-PseAAC was superior to any of the existing predictors in this area.
Source: BioMed Research International
DOI: 10.1155/2014/947416
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $2,680
Awards: G1221076648, G1259219724, G147337110, G1569052824, G1590016485, G1864978289, G27034639, G3110773792, G3383274623, G3664493070, 集成学习框架下的蛋白质-蛋白质结合位点预测方法研究, G3961670147, G4011924711, G4188780153, G4608797612, G5208741891, G5926747656, G6422719664, G6964975264, G7211146731, 基于多源信息融合的受体和抗菌肽分层多标签分类预测模型研究, G783389107, G8150484569, G8622883462, G882106552
OpenAlex ID: W1995173448
