4.6 Review

The interface of protein structure, protein biophysics, and molecular evolution

期刊

PROTEIN SCIENCE
卷 21, 期 6, 页码 769-785

出版社

WILEY
DOI: 10.1002/pro.2071

关键词

evolutionary modeling; domain evolution; sequence-structure-function relationships; protein dynamics; protein thermodynamics; gene duplication; protein expression; ancestral sequence reconstruction

资金

  1. NSF EF [0905606]
  2. University of Southern California, the National Institute of Health [R21EB012281, RO1EY017293, RO1EY017293S1, P30 CA014089]
  3. Norris Comprehensive Cancer Center
  4. Translational Research Laboratory at the School of Pharmacy
  5. American Cancer Society [IRG-58-007-48]
  6. Ming Hsieh Institute for Engineering Medicine for Cancer
  7. Wright Foundation
  8. Stop Cancer Foundation
  9. Engineering and Physical Sciences Research Council [EP/H028064/1, EP/H028064/2] Funding Source: researchfish
  10. Medical Research Council [MC_U117573805, MC_U105161047] Funding Source: researchfish
  11. EPSRC [EP/H028064/2, EP/H028064/1] Funding Source: UKRI
  12. MRC [MC_U105161047, MC_U117573805] Funding Source: UKRI
  13. Direct For Biological Sciences
  14. Div Of Biological Infrastructure [0905606] Funding Source: National Science Foundation
  15. Direct For Biological Sciences
  16. Div Of Molecular and Cellular Bioscience [1021883] Funding Source: National Science Foundation
  17. Division Of Environmental Biology
  18. Direct For Biological Sciences [1132229] Funding Source: National Science Foundation

向作者/读者索取更多资源

The interface of protein structural biology, protein biophysics, molecular evolution, and molecular population genetics forms the foundations for a mechanistic understanding of many aspects of protein biochemistry. Current efforts in interdisciplinary protein modeling are in their infancy and the state-of-the art of such models is described. Beyond the relationship between amino acid substitution and static protein structure, protein function, and corresponding organismal fitness, other considerations are also discussed. More complex mutational processes such as insertion and deletion and domain rearrangements and even circular permutations should be evaluated. The role of intrinsically disordered proteins is still controversial, but may be increasingly important to consider. Protein geometry and protein dynamics as a deviation from static considerations of protein structure are also important. Protein expression level is known to be a major determinant of evolutionary rate and several considerations including selection at the mRNA level and the role of interaction specificity are discussed. Lastly, the relationship between modeling and needed high-throughput experimental data as well as experimental examination of protein evolution using ancestral sequence resurrection and in vitro biochemistry are presented, towards an aim of ultimately generating better models for biological inference and prediction.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据