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Protein Disorder and Short Conserved Motifs in Disordered Regions Are Enriched near the Cytoplasmic Side of Single-Pass Transmembrane Proteins

机译:蛋白障碍和短保守基序无序地区富集接近单次跨膜蛋白的细胞质一侧

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摘要

Intracellular juxtamembrane regions of transmembrane proteins play pivotal roles in cell signalling, mediated by protein-protein interactions. Disordered protein regions, and short conserved motifs within them, are emerging as key determinants of many such interactions. Here, we investigated whether disorder and conserved motifs are enriched in the juxtamembrane area of human single-pass transmembrane proteins. Conserved motifs were defined as short disordered regions that were much more conserved than the adjacent disordered residues. Human single-pass proteins had higher mean disorder in their cytoplasmic segments than their extracellular parts. Some, but not all, of this effect reflected the shorter length of the cytoplasmic tail. A peak of cytoplasmic disorder was seen at around 30 residues from the membrane. We noted a significant increase in the incidence of conserved motifs within the disordered regions at the same location, even after correcting for the extent of disorder. We conclude that elevated disorder within the cytoplasmic tail of many transmembrane proteins is likely to be associated with enrichment for signalling interactions mediated by conserved short motifs.
机译:跨膜蛋白的胞内近膜区在细胞信号转导中起着关键作用,由蛋白间相互作用介导。紊乱的蛋白质区域和其中的短保守基元正在成为许多此类相互作用的关键决定因素。在这里,我们调查了人类单次通过跨膜蛋白近膜区域是否富集了无序和保守的基序。保守的基序被定义为比相邻的无序残基保守得多的短无序区域。人单次通过蛋白在其细胞质部分的平均无序性高于其细胞外部分。这种作用中的一些但不是全部反映了胞质尾巴的长度较短。在膜的大约30个残基处发现了细胞质紊乱的峰值。我们注意到即使校正了疾病的程度,在相同位置的无序区域内保守基序的发生率也显着增加。我们得出的结论是,许多跨膜蛋白胞质尾部内的异常紊乱可能与保守的短基序介导的信号相互作用的富集有关。

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