Consensus Finder web tool to predict stabilizing substitutions in proteins

The consensus sequence approach to predicting stabilizing substitutions in proteins rests on the notion that conserved amino acids are more likely to contribute to the stability of a protein fold than non-conserved amino acids. To implement a prediction for a target protein sequence, one finds homol...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Jones, Bryan J, Kan, Chi Nok Enoch, Luo, Christine, Kazlauskas, Romas J
Format: Buchkapitel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 148
container_issue
container_start_page 129
container_title
container_volume 643
creator Jones, Bryan J
Kan, Chi Nok Enoch
Luo, Christine
Kazlauskas, Romas J
description The consensus sequence approach to predicting stabilizing substitutions in proteins rests on the notion that conserved amino acids are more likely to contribute to the stability of a protein fold than non-conserved amino acids. To implement a prediction for a target protein sequence, one finds homologous sequences and aligns them in a multiple sequence alignment. The sequence of the most frequently occurring amino acid at each position is the consensus sequence. Replacement of a rarely occurring amino acid in the target with a frequently occurring amino acid from the consensus sequence is predicted to be stabilizing. Consensus Finder is an open-source web tool that automates this prediction. This chapter reviews the rationale for the consensus sequence approach and explains the options for fine-tuning this approach using Staphylococcus nuclease A as an example.
doi_str_mv 10.1016/bs.mie.2020.07.010
format Book Chapter
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_2440899673</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2440899673</sourcerecordid><originalsourceid>FETCH-LOGICAL-p255t-6e2d245c343a1960e69c168fdf752ed171a2a6af4557750df4d2da8bc800162f3</originalsourceid><addsrcrecordid>eNo1j81LxDAQxYMg7rr6D3iQHL20JmnzdZTF9YMFL3ouaTOVSJuunRTRv96A62UeA7838x4hV5yVnHF122I5BigFE6xkumScnZA1l1IX2hqzIueIH4wJbSw_I6tKGKvysibP2ykiRFyQ7kL0MNMvaGmapiEPepjBhy5RTK4NQ_gJ8Z3i0mIKaUkhO2mIGZoShIgX5LR3A8LlUTfkbXf_un0s9i8PT9u7fXEQUqZCgfCill1VV45bxUDZjivT-15LAZ5r7oRTrq9zeC2Z72svvDNtZ1guKvpqQ27-7ubHnwtgasaAHQyDizAt2Ii6ZsZapauMXh_RpR3BN4c5jG7-bv77V78wi1y1</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>book_chapter</recordtype><pqid>2440899673</pqid></control><display><type>book_chapter</type><title>Consensus Finder web tool to predict stabilizing substitutions in proteins</title><source>Elsevier ScienceDirect Journals</source><creator>Jones, Bryan J ; Kan, Chi Nok Enoch ; Luo, Christine ; Kazlauskas, Romas J</creator><creatorcontrib>Jones, Bryan J ; Kan, Chi Nok Enoch ; Luo, Christine ; Kazlauskas, Romas J</creatorcontrib><description>The consensus sequence approach to predicting stabilizing substitutions in proteins rests on the notion that conserved amino acids are more likely to contribute to the stability of a protein fold than non-conserved amino acids. To implement a prediction for a target protein sequence, one finds homologous sequences and aligns them in a multiple sequence alignment. The sequence of the most frequently occurring amino acid at each position is the consensus sequence. Replacement of a rarely occurring amino acid in the target with a frequently occurring amino acid from the consensus sequence is predicted to be stabilizing. Consensus Finder is an open-source web tool that automates this prediction. This chapter reviews the rationale for the consensus sequence approach and explains the options for fine-tuning this approach using Staphylococcus nuclease A as an example.</description><identifier>EISSN: 1557-7988</identifier><identifier>DOI: 10.1016/bs.mie.2020.07.010</identifier><identifier>PMID: 32896278</identifier><language>eng</language><publisher>United States</publisher><ispartof>Methods in enzymology, 2020, Vol.643, p.129-148</ispartof><rights>2020 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32896278$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jones, Bryan J</creatorcontrib><creatorcontrib>Kan, Chi Nok Enoch</creatorcontrib><creatorcontrib>Luo, Christine</creatorcontrib><creatorcontrib>Kazlauskas, Romas J</creatorcontrib><title>Consensus Finder web tool to predict stabilizing substitutions in proteins</title><title>Methods in enzymology</title><addtitle>Methods Enzymol</addtitle><description>The consensus sequence approach to predicting stabilizing substitutions in proteins rests on the notion that conserved amino acids are more likely to contribute to the stability of a protein fold than non-conserved amino acids. To implement a prediction for a target protein sequence, one finds homologous sequences and aligns them in a multiple sequence alignment. The sequence of the most frequently occurring amino acid at each position is the consensus sequence. Replacement of a rarely occurring amino acid in the target with a frequently occurring amino acid from the consensus sequence is predicted to be stabilizing. Consensus Finder is an open-source web tool that automates this prediction. This chapter reviews the rationale for the consensus sequence approach and explains the options for fine-tuning this approach using Staphylococcus nuclease A as an example.</description><issn>1557-7988</issn><fulltext>true</fulltext><rsrctype>book_chapter</rsrctype><creationdate>2020</creationdate><recordtype>book_chapter</recordtype><recordid>eNo1j81LxDAQxYMg7rr6D3iQHL20JmnzdZTF9YMFL3ouaTOVSJuunRTRv96A62UeA7838x4hV5yVnHF122I5BigFE6xkumScnZA1l1IX2hqzIueIH4wJbSw_I6tKGKvysibP2ykiRFyQ7kL0MNMvaGmapiEPepjBhy5RTK4NQ_gJ8Z3i0mIKaUkhO2mIGZoShIgX5LR3A8LlUTfkbXf_un0s9i8PT9u7fXEQUqZCgfCill1VV45bxUDZjivT-15LAZ5r7oRTrq9zeC2Z72svvDNtZ1guKvpqQ27-7ubHnwtgasaAHQyDizAt2Ii6ZsZapauMXh_RpR3BN4c5jG7-bv77V78wi1y1</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Jones, Bryan J</creator><creator>Kan, Chi Nok Enoch</creator><creator>Luo, Christine</creator><creator>Kazlauskas, Romas J</creator><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>2020</creationdate><title>Consensus Finder web tool to predict stabilizing substitutions in proteins</title><author>Jones, Bryan J ; Kan, Chi Nok Enoch ; Luo, Christine ; Kazlauskas, Romas J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p255t-6e2d245c343a1960e69c168fdf752ed171a2a6af4557750df4d2da8bc800162f3</frbrgroupid><rsrctype>book_chapters</rsrctype><prefilter>book_chapters</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jones, Bryan J</creatorcontrib><creatorcontrib>Kan, Chi Nok Enoch</creatorcontrib><creatorcontrib>Luo, Christine</creatorcontrib><creatorcontrib>Kazlauskas, Romas J</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jones, Bryan J</au><au>Kan, Chi Nok Enoch</au><au>Luo, Christine</au><au>Kazlauskas, Romas J</au><format>book</format><genre>bookitem</genre><ristype>CHAP</ristype><atitle>Consensus Finder web tool to predict stabilizing substitutions in proteins</atitle><btitle>Methods in enzymology</btitle><addtitle>Methods Enzymol</addtitle><date>2020</date><risdate>2020</risdate><volume>643</volume><spage>129</spage><epage>148</epage><pages>129-148</pages><eissn>1557-7988</eissn><abstract>The consensus sequence approach to predicting stabilizing substitutions in proteins rests on the notion that conserved amino acids are more likely to contribute to the stability of a protein fold than non-conserved amino acids. To implement a prediction for a target protein sequence, one finds homologous sequences and aligns them in a multiple sequence alignment. The sequence of the most frequently occurring amino acid at each position is the consensus sequence. Replacement of a rarely occurring amino acid in the target with a frequently occurring amino acid from the consensus sequence is predicted to be stabilizing. Consensus Finder is an open-source web tool that automates this prediction. This chapter reviews the rationale for the consensus sequence approach and explains the options for fine-tuning this approach using Staphylococcus nuclease A as an example.</abstract><cop>United States</cop><pmid>32896278</pmid><doi>10.1016/bs.mie.2020.07.010</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier EISSN: 1557-7988
ispartof Methods in enzymology, 2020, Vol.643, p.129-148
issn 1557-7988
language eng
recordid cdi_proquest_miscellaneous_2440899673
source Elsevier ScienceDirect Journals
title Consensus Finder web tool to predict stabilizing substitutions in proteins
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T18%3A33%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=bookitem&rft.atitle=Consensus%20Finder%20web%20tool%20to%20predict%20stabilizing%20substitutions%20in%20proteins&rft.btitle=Methods%20in%20enzymology&rft.au=Jones,%20Bryan%20J&rft.date=2020&rft.volume=643&rft.spage=129&rft.epage=148&rft.pages=129-148&rft.eissn=1557-7988&rft_id=info:doi/10.1016/bs.mie.2020.07.010&rft_dat=%3Cproquest_pubme%3E2440899673%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2440899673&rft_id=info:pmid/32896278&rfr_iscdi=true