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Proteins in the slow lane

机译:慢车道中的蛋白质

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摘要

Protein evolution occurs only slowly, since most amino-acid substitutions are likely to be deleterious and selection will favour conservation of function. Inna Povolotskaya and Fyodor Kondrashov set out to find out just how slowly by asking the question, are ancient extant proteins - those that were present in the last universal common ancestorrn(LUCA) - continuing to diverge from the ancestral sequence? Their calculations, based on the approach used by Edwin Hubble in his study of the recession of galaxies in the physical Universe, suggests that extant protein sequences are still expanding from each other, and, therefore, from their common ancestor. Divergence is very slow: the 3.5 billion years or so since LUCAs time has not been long enough for the limit of sequence divergence to be reached. This tardiness is a consequence of the sparseness of functional protein sequences in sequence space and the ruggedness of the protein fitness landscape: 98% of sites cannot accept an amino-acid substitution at a given moment, yet most sites may eventually be permitted to evolve when other, compensatory, changes occur.
机译:蛋白质进化只发生得很慢,因为大多数氨基酸取代很可能有害,选择有利于功能的保守。 Inna Povolotskaya和Fyodor Kondrashov着手问这个问题,发现古老的现存蛋白质(存在于最后一个通用共同祖先(LUCA)中的那些蛋白质)继续从祖先序列中分化出来是多么缓慢?他们的计算基于埃德温·哈勃(Edwin Hubble)在研究物理宇宙中银河系退缩时所使用的方法,表明现存的蛋白质序列仍在彼此之间扩展,因此也从它们的共同祖先开始扩展。散度非常慢:自LUCA以来大约35亿年的时间还不够长,无法达到序列散度的极限。这种迟缓是由于序列空间中功能性蛋白质序列稀疏和蛋白质适应性格局的崎a性的结果:98%的位点在给定的时刻不能接受氨基酸取代,但是大多数位点最终可能被允许进化。其他(补偿性)变化会发生。

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  • 来源
    《Nature》 |2010年第7300期|P.843|共1页
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  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 入库时间 2022-08-18 02:55:08

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