Engineering allostery into proteins
Advances in Experimental Medicine and Biology, ISSN: 2214-8019, Vol: 1163, Page: 359-384
2019
- 14Citations
- 21Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations14
- Citation Indexes13
- 13
- CrossRef3
- Patent Family Citations1
- Patent Families1
- Captures21
- Readers21
- 21
Book Chapter Description
Our ability to engineer protein structure and function has grown dramatically over recent years. Perhaps the next level in protein design is to develop proteins whose function can be regulated in response to various stimuli, including ligand binding, pH changes, and light. Endeavors toward these goals have tested and expanded on our understanding of protein function and allosteric regulation. In this chapter, we provide examples from different methods for developing new allosterically regulated proteins. These methods range from whole insertion of regulatory domains into new host proteins, to covalent attachment of photoswitches to generate light-responsive proteins, and to targeted changes to specific amino acid residues, especially to residues identified to be important for relaying allosteric information across the protein framework. Many of the examples we discuss have already found practical use in medical and biotechnology applications.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85074742537&origin=inward; http://dx.doi.org/10.1007/978-981-13-8719-7_15; http://www.ncbi.nlm.nih.gov/pubmed/31707711; http://link.springer.com/10.1007/978-981-13-8719-7_15; https://dx.doi.org/10.1007/978-981-13-8719-7_15; https://link.springer.com/chapter/10.1007/978-981-13-8719-7_15
Springer Science and Business Media LLC
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