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Natural protein sequences are more intrinsically disordered than random sequences.
Yu, Jia-Feng; Cao, Zanxia; Yang, Yuedong; Wang, Chun-Ling; Su, Zhen-Dong; Zhao, Ya-Wei; Wang, Ji-Hua; Zhou, Yaoqi.
Afiliação
  • Yu JF; Shandong Provincial Key Laboratory of Biophysics, Institute of Biophysics, Dezhou University, Dezhou, 253023, China.
  • Cao Z; Shandong Provincial Key Laboratory of Biophysics, Institute of Biophysics, Dezhou University, Dezhou, 253023, China.
  • Yang Y; College of Physics and Electronic Information, Dezhou University, Dezhou, 253023, China.
  • Wang CL; Institute for Glycomics and School of Information and Communication Technology, Griffith University, Parklands Dr, Southport, QLD, 4222, Australia.
  • Su ZD; College of Physics and Electronic Information, Dezhou University, Dezhou, 253023, China.
  • Zhao YW; Shandong Provincial Key Laboratory of Biophysics, Institute of Biophysics, Dezhou University, Dezhou, 253023, China.
  • Wang JH; Shandong Provincial Key Laboratory of Biophysics, Institute of Biophysics, Dezhou University, Dezhou, 253023, China.
  • Zhou Y; Shandong Provincial Key Laboratory of Biophysics, Institute of Biophysics, Dezhou University, Dezhou, 253023, China.
Cell Mol Life Sci ; 73(15): 2949-57, 2016 08.
Article em En | MEDLINE | ID: mdl-26801222
ABSTRACT
Most natural protein sequences have resulted from millions or even billions of years of evolution. How they differ from random sequences is not fully understood. Previous computational and experimental studies of random proteins generated from noncoding regions yielded inclusive results due to species-dependent codon biases and GC contents. Here, we approach this problem by investigating 10,000 sequences randomized at the amino acid level. Using well-established predictors for protein intrinsic disorder, we found that natural sequences have more long disordered regions than random sequences, even when random and natural sequences have the same overall composition of amino acid residues. We also showed that random sequences are as structured as natural sequences according to contents and length distributions of predicted secondary structure, although the structures from random sequences may be in a molten globular-like state, according to molecular dynamics simulations. The bias of natural sequences toward more intrinsic disorder suggests that natural sequences are created and evolved to avoid protein aggregation and increase functional diversity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Proteínas Intrinsicamente Desordenadas Tipo de estudo: Clinical_trials Idioma: En Revista: Cell Mol Life Sci Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Proteínas Intrinsicamente Desordenadas Tipo de estudo: Clinical_trials Idioma: En Revista: Cell Mol Life Sci Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China