Sequencing, biochemical characterization, crystal structure and molecular dynamics of cellobiohydrolase Cel7A from Geotrichum candidum 3C
The ascomycete Geotrichum candidum is a versatile and efficient decay fungus that is involved, for example, in biodeterioration of compact discs; notably, the 3C strain was previously shown to degrade filter paper and cotton more efficiently than several industrial enzyme preparations. Glycoside hyd...
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creator | Borisova, Anna S Eneyskaya, Elena V Bobrov, Kirill S Jana, Suvamay Logachev, Anton Polev, Dmitrii E Lapidus, Alla L Ibatullin, Farid M Saleem, Umair Sandgren, Mats Payne, Christina M Kulminskaya, Anna A Ståhlberg, Jerry |
description | The ascomycete Geotrichum candidum is a versatile and efficient decay fungus that is involved, for example, in biodeterioration of compact discs; notably, the 3C strain was previously shown to degrade filter paper and cotton more efficiently than several industrial enzyme preparations. Glycoside hydrolase (GH) family 7 cellobiohydrolases (CBHs) are the primary constituents of industrial cellulase cocktails employed in biomass conversion, and feature tunnel‐enclosed active sites that enable processive hydrolytic cleavage of cellulose chains. Understanding the structure–function relationships defining the activity and stability of GH7 CBHs is thus of keen interest. Accordingly, we report the comprehensive characterization of the GH7 CBH secreted by G. candidum (GcaCel7A). The bimodular cellulase consists of a family 1 cellulose‐binding module (CBM) and linker connected to a GH7 catalytic domain that shares 64% sequence identity with the archetypal industrial GH7 CBH of Hypocrea jecorina (HjeCel7A). GcaCel7A shows activity on Avicel cellulose similar to HjeCel7A, with less product inhibition, but has a lower temperature optimum (50 °C versus 60–65 °C, respectively). Five crystal structures, with and without bound thio‐oligosaccharides, show conformational diversity of tunnel‐enclosing loops, including a form with partial tunnel collapse at subsite –4 not reported previously in GH7. Also, the first O‐glycosylation site in a GH7 crystal structure is reported – on a loop where the glycan probably influences loop contacts across the active site and interactions with the cellulose surface. The GcaCel7A structures indicate higher loop flexibility than HjeCel7A, in accordance with sequence modifications. However, GcaCel7A retains small fluctuations in molecular simulations, suggesting high processivity and low endo‐initiation probability, similar to HjeCel7A. DATABASE: Structural data are available in the Protein Data Bank under the accession numbers 5AMP, 4ZZV, 4ZZW, 4ZZT, and 4ZZU. The Geotrichum candidum GH family 7 cellobiohydrolase nucleotide sequence is available in GenBank under accession number KJ958925. ENZYMES: Glycoside hydrolase family 7 reducing end acting cellobiohydrolase. |
doi_str_mv | 10.1111/febs.13509 |
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Glycoside hydrolase (GH) family 7 cellobiohydrolases (CBHs) are the primary constituents of industrial cellulase cocktails employed in biomass conversion, and feature tunnel‐enclosed active sites that enable processive hydrolytic cleavage of cellulose chains. Understanding the structure–function relationships defining the activity and stability of GH7 CBHs is thus of keen interest. Accordingly, we report the comprehensive characterization of the GH7 CBH secreted by G. candidum (GcaCel7A). The bimodular cellulase consists of a family 1 cellulose‐binding module (CBM) and linker connected to a GH7 catalytic domain that shares 64% sequence identity with the archetypal industrial GH7 CBH of Hypocrea jecorina (HjeCel7A). GcaCel7A shows activity on Avicel cellulose similar to HjeCel7A, with less product inhibition, but has a lower temperature optimum (50 °C versus 60–65 °C, respectively). Five crystal structures, with and without bound thio‐oligosaccharides, show conformational diversity of tunnel‐enclosing loops, including a form with partial tunnel collapse at subsite –4 not reported previously in GH7. Also, the first O‐glycosylation site in a GH7 crystal structure is reported – on a loop where the glycan probably influences loop contacts across the active site and interactions with the cellulose surface. The GcaCel7A structures indicate higher loop flexibility than HjeCel7A, in accordance with sequence modifications. However, GcaCel7A retains small fluctuations in molecular simulations, suggesting high processivity and low endo‐initiation probability, similar to HjeCel7A. DATABASE: Structural data are available in the Protein Data Bank under the accession numbers 5AMP, 4ZZV, 4ZZW, 4ZZT, and 4ZZU. The Geotrichum candidum GH family 7 cellobiohydrolase nucleotide sequence is available in GenBank under accession number KJ958925. ENZYMES: Glycoside hydrolase family 7 reducing end acting cellobiohydrolase.</description><identifier>ISSN: 1742-464X</identifier><identifier>EISSN: 1742-4658</identifier><identifier>DOI: 10.1111/febs.13509</identifier><identifier>PMID: 26367132</identifier><language>eng</language><publisher>England: Published by Blackwell Pub. on behalf of the Federation of European Biochemical Societies</publisher><subject>active sites ; Amino Acid Sequence ; Ascomycetes ; Biocatalysis and Enzyme Technology ; Biochemistry and Molecular Biology ; biodegradation ; Biokatalys och enzymteknik ; Biokemi och molekylärbiologi ; biomass ; biomass degradation ; cellulase ; cellulose ; cellulose 1,4-beta-cellobiosidase ; Cellulose 1,4-beta-Cellobiosidase - chemistry ; Cellulose 1,4-beta-Cellobiosidase - genetics ; Cellulose 1,4-beta-Cellobiosidase - metabolism ; cotton ; crystal structure ; decay fungi ; endo-1,4-beta-glucanase ; Förnyelsebar bioenergi ; genetic databases ; Geotrichum - enzymology ; Geotrichum candidum ; glycosides ; Hydrogen-Ion Concentration ; Hypocrea jecorina ; Kinetics ; molecular dynamics ; Molecular Dynamics Simulation ; Molecular Sequence Data ; nucleotide sequences ; probability ; Protein Conformation ; Renewable Bioenergy Research ; Sequence Alignment ; sequence analysis ; Structural Biology ; structure-activity relationships ; Strukturbiologi ; Temperature ; Trichoderma reesei ; X‐ray structure</subject><ispartof>The FEBS journal, 2015-12, Vol.282 (23), p.4515-4537</ispartof><rights>2015 FEBS</rights><rights>2015 FEBS.</rights><rights>Copyright © 2015 Federation of European Biochemical Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5589-9f88dd79ba6da9b1cfc8bf5e7f5718a5bb6f3218cde245e0f1c3c8158444965a3</citedby><cites>FETCH-LOGICAL-c5589-9f88dd79ba6da9b1cfc8bf5e7f5718a5bb6f3218cde245e0f1c3c8158444965a3</cites><orcidid>0000-0003-4059-8580</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ffebs.13509$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ffebs.13509$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26367132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://res.slu.se/id/publ/73386$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Borisova, Anna S</creatorcontrib><creatorcontrib>Eneyskaya, Elena V</creatorcontrib><creatorcontrib>Bobrov, Kirill S</creatorcontrib><creatorcontrib>Jana, Suvamay</creatorcontrib><creatorcontrib>Logachev, Anton</creatorcontrib><creatorcontrib>Polev, Dmitrii E</creatorcontrib><creatorcontrib>Lapidus, Alla L</creatorcontrib><creatorcontrib>Ibatullin, Farid M</creatorcontrib><creatorcontrib>Saleem, Umair</creatorcontrib><creatorcontrib>Sandgren, Mats</creatorcontrib><creatorcontrib>Payne, Christina M</creatorcontrib><creatorcontrib>Kulminskaya, Anna A</creatorcontrib><creatorcontrib>Ståhlberg, Jerry</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</creatorcontrib><title>Sequencing, biochemical characterization, crystal structure and molecular dynamics of cellobiohydrolase Cel7A from Geotrichum candidum 3C</title><title>The FEBS journal</title><addtitle>FEBS J</addtitle><description>The ascomycete Geotrichum candidum is a versatile and efficient decay fungus that is involved, for example, in biodeterioration of compact discs; notably, the 3C strain was previously shown to degrade filter paper and cotton more efficiently than several industrial enzyme preparations. Glycoside hydrolase (GH) family 7 cellobiohydrolases (CBHs) are the primary constituents of industrial cellulase cocktails employed in biomass conversion, and feature tunnel‐enclosed active sites that enable processive hydrolytic cleavage of cellulose chains. Understanding the structure–function relationships defining the activity and stability of GH7 CBHs is thus of keen interest. Accordingly, we report the comprehensive characterization of the GH7 CBH secreted by G. candidum (GcaCel7A). The bimodular cellulase consists of a family 1 cellulose‐binding module (CBM) and linker connected to a GH7 catalytic domain that shares 64% sequence identity with the archetypal industrial GH7 CBH of Hypocrea jecorina (HjeCel7A). GcaCel7A shows activity on Avicel cellulose similar to HjeCel7A, with less product inhibition, but has a lower temperature optimum (50 °C versus 60–65 °C, respectively). Five crystal structures, with and without bound thio‐oligosaccharides, show conformational diversity of tunnel‐enclosing loops, including a form with partial tunnel collapse at subsite –4 not reported previously in GH7. Also, the first O‐glycosylation site in a GH7 crystal structure is reported – on a loop where the glycan probably influences loop contacts across the active site and interactions with the cellulose surface. The GcaCel7A structures indicate higher loop flexibility than HjeCel7A, in accordance with sequence modifications. However, GcaCel7A retains small fluctuations in molecular simulations, suggesting high processivity and low endo‐initiation probability, similar to HjeCel7A. DATABASE: Structural data are available in the Protein Data Bank under the accession numbers 5AMP, 4ZZV, 4ZZW, 4ZZT, and 4ZZU. The Geotrichum candidum GH family 7 cellobiohydrolase nucleotide sequence is available in GenBank under accession number KJ958925. ENZYMES: Glycoside hydrolase family 7 reducing end acting cellobiohydrolase.</description><subject>active sites</subject><subject>Amino Acid Sequence</subject><subject>Ascomycetes</subject><subject>Biocatalysis and Enzyme Technology</subject><subject>Biochemistry and Molecular Biology</subject><subject>biodegradation</subject><subject>Biokatalys och enzymteknik</subject><subject>Biokemi och molekylärbiologi</subject><subject>biomass</subject><subject>biomass degradation</subject><subject>cellulase</subject><subject>cellulose</subject><subject>cellulose 1,4-beta-cellobiosidase</subject><subject>Cellulose 1,4-beta-Cellobiosidase - chemistry</subject><subject>Cellulose 1,4-beta-Cellobiosidase - genetics</subject><subject>Cellulose 1,4-beta-Cellobiosidase - metabolism</subject><subject>cotton</subject><subject>crystal structure</subject><subject>decay fungi</subject><subject>endo-1,4-beta-glucanase</subject><subject>Förnyelsebar bioenergi</subject><subject>genetic databases</subject><subject>Geotrichum - enzymology</subject><subject>Geotrichum candidum</subject><subject>glycosides</subject><subject>Hydrogen-Ion Concentration</subject><subject>Hypocrea jecorina</subject><subject>Kinetics</subject><subject>molecular dynamics</subject><subject>Molecular Dynamics Simulation</subject><subject>Molecular Sequence Data</subject><subject>nucleotide sequences</subject><subject>probability</subject><subject>Protein Conformation</subject><subject>Renewable Bioenergy Research</subject><subject>Sequence Alignment</subject><subject>sequence analysis</subject><subject>Structural Biology</subject><subject>structure-activity relationships</subject><subject>Strukturbiologi</subject><subject>Temperature</subject><subject>Trichoderma reesei</subject><subject>X‐ray structure</subject><issn>1742-464X</issn><issn>1742-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAURiMEou3AhgcAS2wq1BQ7_s2yjNqCVInFUImd5TjXHVdJPNiJqvAGvDUe0s6CBcKba8nnHvv6K4o3BJ-TvD46aNI5oRzXz4pjIllVMsHV88OefT8qTlK6x5hyVtcvi6NKUCEJrY6LXxv4McFg_XB3hhof7BZ6b02H7NZEY0eI_qcZfRjOkI1zGvNJGuNkxykCMkOL-tCBnToTUTsPJvcmFByy0HUh67ZzG0NnEqA1dPICuRh6dA1hjN5upx7ZrPBt3tD1q-KFM12C1491VdxeXX5bfy5vvl5_WV_clJZzVZe1U6ptZd0Y0Zq6IdZZ1TgO0nFJlOFNIxytiLItVIwDdsRSqwhXjLFacENXRbl40wPspkbvou9NnHUwXqduakzcF51AS0qVyPzpwu9iyF-VRt37tJ_PDBCmpImUQjChpPoPVGAlcio8o-__Qu_DFIc8eKa4rBhl-fpV8WGhbAwpRXCH1xKs99nrffb6T_YZfvuonJoe2gP6FHYGyAI8-A7mf6j01eWnzZP03dLjTNDmLvqkbzcVJgJjrDDmNf0Nk2bFPQ</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Borisova, Anna S</creator><creator>Eneyskaya, Elena V</creator><creator>Bobrov, Kirill S</creator><creator>Jana, Suvamay</creator><creator>Logachev, Anton</creator><creator>Polev, Dmitrii E</creator><creator>Lapidus, Alla L</creator><creator>Ibatullin, Farid M</creator><creator>Saleem, Umair</creator><creator>Sandgren, Mats</creator><creator>Payne, Christina M</creator><creator>Kulminskaya, Anna A</creator><creator>Ståhlberg, Jerry</creator><general>Published by Blackwell Pub. on behalf of the Federation of European Biochemical Societies</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope><orcidid>https://orcid.org/0000-0003-4059-8580</orcidid></search><sort><creationdate>201512</creationdate><title>Sequencing, biochemical characterization, crystal structure and molecular dynamics of cellobiohydrolase Cel7A from Geotrichum candidum 3C</title><author>Borisova, Anna S ; Eneyskaya, Elena V ; Bobrov, Kirill S ; Jana, Suvamay ; Logachev, Anton ; Polev, Dmitrii E ; Lapidus, Alla L ; Ibatullin, Farid M ; Saleem, Umair ; Sandgren, Mats ; Payne, Christina M ; Kulminskaya, Anna A ; Ståhlberg, Jerry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5589-9f88dd79ba6da9b1cfc8bf5e7f5718a5bb6f3218cde245e0f1c3c8158444965a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>active sites</topic><topic>Amino Acid Sequence</topic><topic>Ascomycetes</topic><topic>Biocatalysis and Enzyme Technology</topic><topic>Biochemistry and Molecular Biology</topic><topic>biodegradation</topic><topic>Biokatalys och enzymteknik</topic><topic>Biokemi och molekylärbiologi</topic><topic>biomass</topic><topic>biomass degradation</topic><topic>cellulase</topic><topic>cellulose</topic><topic>cellulose 1,4-beta-cellobiosidase</topic><topic>Cellulose 1,4-beta-Cellobiosidase - chemistry</topic><topic>Cellulose 1,4-beta-Cellobiosidase - genetics</topic><topic>Cellulose 1,4-beta-Cellobiosidase - metabolism</topic><topic>cotton</topic><topic>crystal structure</topic><topic>decay fungi</topic><topic>endo-1,4-beta-glucanase</topic><topic>Förnyelsebar bioenergi</topic><topic>genetic databases</topic><topic>Geotrichum - enzymology</topic><topic>Geotrichum candidum</topic><topic>glycosides</topic><topic>Hydrogen-Ion Concentration</topic><topic>Hypocrea jecorina</topic><topic>Kinetics</topic><topic>molecular dynamics</topic><topic>Molecular Dynamics Simulation</topic><topic>Molecular Sequence Data</topic><topic>nucleotide sequences</topic><topic>probability</topic><topic>Protein Conformation</topic><topic>Renewable Bioenergy Research</topic><topic>Sequence Alignment</topic><topic>sequence analysis</topic><topic>Structural Biology</topic><topic>structure-activity relationships</topic><topic>Strukturbiologi</topic><topic>Temperature</topic><topic>Trichoderma reesei</topic><topic>X‐ray structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borisova, Anna S</creatorcontrib><creatorcontrib>Eneyskaya, Elena V</creatorcontrib><creatorcontrib>Bobrov, Kirill S</creatorcontrib><creatorcontrib>Jana, Suvamay</creatorcontrib><creatorcontrib>Logachev, Anton</creatorcontrib><creatorcontrib>Polev, Dmitrii E</creatorcontrib><creatorcontrib>Lapidus, Alla L</creatorcontrib><creatorcontrib>Ibatullin, Farid M</creatorcontrib><creatorcontrib>Saleem, Umair</creatorcontrib><creatorcontrib>Sandgren, Mats</creatorcontrib><creatorcontrib>Payne, Christina M</creatorcontrib><creatorcontrib>Kulminskaya, Anna A</creatorcontrib><creatorcontrib>Ståhlberg, Jerry</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>The FEBS journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borisova, Anna S</au><au>Eneyskaya, Elena V</au><au>Bobrov, Kirill S</au><au>Jana, Suvamay</au><au>Logachev, Anton</au><au>Polev, Dmitrii E</au><au>Lapidus, Alla L</au><au>Ibatullin, Farid M</au><au>Saleem, Umair</au><au>Sandgren, Mats</au><au>Payne, Christina M</au><au>Kulminskaya, Anna A</au><au>Ståhlberg, Jerry</au><aucorp>Sveriges lantbruksuniversitet</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequencing, biochemical characterization, crystal structure and molecular dynamics of cellobiohydrolase Cel7A from Geotrichum candidum 3C</atitle><jtitle>The FEBS journal</jtitle><addtitle>FEBS J</addtitle><date>2015-12</date><risdate>2015</risdate><volume>282</volume><issue>23</issue><spage>4515</spage><epage>4537</epage><pages>4515-4537</pages><issn>1742-464X</issn><eissn>1742-4658</eissn><abstract>The ascomycete Geotrichum candidum is a versatile and efficient decay fungus that is involved, for example, in biodeterioration of compact discs; notably, the 3C strain was previously shown to degrade filter paper and cotton more efficiently than several industrial enzyme preparations. Glycoside hydrolase (GH) family 7 cellobiohydrolases (CBHs) are the primary constituents of industrial cellulase cocktails employed in biomass conversion, and feature tunnel‐enclosed active sites that enable processive hydrolytic cleavage of cellulose chains. Understanding the structure–function relationships defining the activity and stability of GH7 CBHs is thus of keen interest. Accordingly, we report the comprehensive characterization of the GH7 CBH secreted by G. candidum (GcaCel7A). The bimodular cellulase consists of a family 1 cellulose‐binding module (CBM) and linker connected to a GH7 catalytic domain that shares 64% sequence identity with the archetypal industrial GH7 CBH of Hypocrea jecorina (HjeCel7A). GcaCel7A shows activity on Avicel cellulose similar to HjeCel7A, with less product inhibition, but has a lower temperature optimum (50 °C versus 60–65 °C, respectively). Five crystal structures, with and without bound thio‐oligosaccharides, show conformational diversity of tunnel‐enclosing loops, including a form with partial tunnel collapse at subsite –4 not reported previously in GH7. Also, the first O‐glycosylation site in a GH7 crystal structure is reported – on a loop where the glycan probably influences loop contacts across the active site and interactions with the cellulose surface. The GcaCel7A structures indicate higher loop flexibility than HjeCel7A, in accordance with sequence modifications. However, GcaCel7A retains small fluctuations in molecular simulations, suggesting high processivity and low endo‐initiation probability, similar to HjeCel7A. DATABASE: Structural data are available in the Protein Data Bank under the accession numbers 5AMP, 4ZZV, 4ZZW, 4ZZT, and 4ZZU. The Geotrichum candidum GH family 7 cellobiohydrolase nucleotide sequence is available in GenBank under accession number KJ958925. ENZYMES: Glycoside hydrolase family 7 reducing end acting cellobiohydrolase.</abstract><cop>England</cop><pub>Published by Blackwell Pub. on behalf of the Federation of European Biochemical Societies</pub><pmid>26367132</pmid><doi>10.1111/febs.13509</doi><tpages>23</tpages><orcidid>https://orcid.org/0000-0003-4059-8580</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | active sites Amino Acid Sequence Ascomycetes Biocatalysis and Enzyme Technology Biochemistry and Molecular Biology biodegradation Biokatalys och enzymteknik Biokemi och molekylärbiologi biomass biomass degradation cellulase cellulose cellulose 1,4-beta-cellobiosidase Cellulose 1,4-beta-Cellobiosidase - chemistry Cellulose 1,4-beta-Cellobiosidase - genetics Cellulose 1,4-beta-Cellobiosidase - metabolism cotton crystal structure decay fungi endo-1,4-beta-glucanase Förnyelsebar bioenergi genetic databases Geotrichum - enzymology Geotrichum candidum glycosides Hydrogen-Ion Concentration Hypocrea jecorina Kinetics molecular dynamics Molecular Dynamics Simulation Molecular Sequence Data nucleotide sequences probability Protein Conformation Renewable Bioenergy Research Sequence Alignment sequence analysis Structural Biology structure-activity relationships Strukturbiologi Temperature Trichoderma reesei X‐ray structure |
title | Sequencing, biochemical characterization, crystal structure and molecular dynamics of cellobiohydrolase Cel7A from Geotrichum candidum 3C |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T02%3A22%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sequencing,%20biochemical%20characterization,%20crystal%20structure%20and%20molecular%20dynamics%20of%20cellobiohydrolase%20Cel7A%20from%20Geotrichum%20candidum%203C&rft.jtitle=The%20FEBS%20journal&rft.au=Borisova,%20Anna%20S&rft.aucorp=Sveriges%20lantbruksuniversitet&rft.date=2015-12&rft.volume=282&rft.issue=23&rft.spage=4515&rft.epage=4537&rft.pages=4515-4537&rft.issn=1742-464X&rft.eissn=1742-4658&rft_id=info:doi/10.1111/febs.13509&rft_dat=%3Cproquest_swepu%3E1776646878%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1757243473&rft_id=info:pmid/26367132&rfr_iscdi=true |