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球状蛋白质中与构象相关序列的编码分析。期望信息的理论与应用。

Analysis of code relating sequences to conformation in globular prtoeins. Theory and application of expected information.

作者信息

Robson B

出版信息

Biochem J. 1974 Sep;141(3):853-67. doi: 10.1042/bj1410853.

Abstract
  1. An information theory analysis of the folding of a globular protein is proposed. 2. The folding is seen as a transfer of information between two messages, the primary sequence and the biologically active conformation. 3. It is shown how the information transferred was estimated by inspection of proteins of known primary sequence and conformation. 4. In this estimation, concerted use of subjective (Bayesian) probabilities leads to a more robust approach which can be employed whether the number of proteins of known sequence and conformation is large or small. 5. Further, it is demonstrated that the problem then becomes a very simple algebraic formulation for information estimates. 6. Finally, it is shown how this process of information theory analysis can be reversed to predict the conformation of a protein by using its primary sequence and the above information estimates obtained from other proteins. 7. The present paper provides the theoretical basis for the derivation and application of a stereochemical alphabet (Robson & Pain, 1974a,c), and for an investigation of the effects of residues on the conformations of their neighbours (Robson & Pain, 1974b).
摘要
  1. 提出了一种对球状蛋白质折叠的信息论分析方法。2. 蛋白质折叠被视为两种信息之间的传递,即一级序列和生物活性构象。3. 展示了如何通过检查已知一级序列和构象的蛋白质来估计传递的信息。4. 在这种估计中,协同使用主观(贝叶斯)概率会产生一种更稳健的方法,无论已知序列和构象的蛋白质数量是多还是少,都可以采用。5. 此外,证明了该问题随后对于信息估计而言会变成一个非常简单的代数公式。6. 最后,展示了如何通过使用蛋白质的一级序列以及从其他蛋白质获得的上述信息估计来反转这个信息论分析过程,从而预测蛋白质的构象。7. 本文为立体化学字母表(罗布森和佩恩,1974a,c)的推导和应用,以及对残基对其相邻残基构象影响的研究(罗布森和佩恩,1974b)提供了理论基础。

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引用本文的文献

本文引用的文献

1
The tertiary structure of ribonuclease.
Brookhaven Symp Biol. 1962 Dec;15:184-98.
7
Protein denaturation.蛋白质变性
Adv Protein Chem. 1968;23:121-282. doi: 10.1016/s0065-3233(08)60401-5.
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Directional information transfer in protein helices.
Nat New Biol. 1972 Jul 26;238(82):107-8. doi: 10.1038/newbio238107a0.

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