Molecular architecture of KedS8, a sugar N ‐methyltransferase from S treptoalloteichus sp. ATCC 53650

Kedarcidin, produced by Streptoalloteichus sp. ATCC 53650, is a fascinating chromoprotein of 114 amino acid residues that displays both antibiotic and anticancer activity. The chromophore responsible for its chemotherapeutic activity is an ansa‐bridged enediyne with two attached sugars, l ‐mycarose,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Protein science 2015-10, Vol.24 (10), p.1593-1599
Hauptverfasser: Delvaux, Nathan A., Thoden, James B., Holden, Hazel M.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1599
container_issue 10
container_start_page 1593
container_title Protein science
container_volume 24
creator Delvaux, Nathan A.
Thoden, James B.
Holden, Hazel M.
description Kedarcidin, produced by Streptoalloteichus sp. ATCC 53650, is a fascinating chromoprotein of 114 amino acid residues that displays both antibiotic and anticancer activity. The chromophore responsible for its chemotherapeutic activity is an ansa‐bridged enediyne with two attached sugars, l ‐mycarose, and l ‐kedarosamine. The biosynthesis of l ‐kedarosamine, a highly unusual trideoxysugar, is beginning to be revealed through bioinformatics approaches. One of the enzymes putatively involved in the production of this carbohydrate is referred to as KedS8. It has been proposed that KedS8 is an N ‐methyltransferase that utilizes S ‐adenosylmethionine as the methyl donor and a dTDP‐linked C‐4′ amino sugar as the substrate. Here we describe the three‐dimensional architecture of KedS8 in complex with S ‐adenosylhomocysteine. The structure was solved to 2.0 Å resolution and refined to an overall R ‐factor of 17.1%. Unlike that observed for other sugar N ‐methyltransferases, KedS8 adopts a novel tetrameric quaternary structure due to the swapping of β‐strands at the N‐termini of its subunits. The structure presented here represents the first example of an N ‐methyltransferase that functions on C‐4′ rather than C‐3′ amino sugars.
doi_str_mv 10.1002/pro.2742
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1002_pro_2742</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1002_pro_2742</sourcerecordid><originalsourceid>FETCH-LOGICAL-c722-383c963791c9b12fa94bcbfb7602a63620eac5396c4ecc2e240f38cbab5d7d453</originalsourceid><addsrcrecordid>eNotkL1OwzAURi0EEqUg8QgeGUjwX5x4rCIoiAJDO7BFzu11U5TiyHaGbjwCz8iT0Aqmo09H-oZDyDVnOWdM3A3B56JU4oRMuNImq4x-PyUTZjTPKqmrc3IR4wdjTHEhJ2Tz4nuEsbeB2gDdNiGkMSD1jj7jelndUkvjuDnoV_rz9b3D1O37FOxndBhsROqC39ElTQGH5G3f-4Rb6MZI45DT2aquaSF1wS7JmbN9xKt_Tsnq4X5VP2aLt_lTPVtkUAqRyUqC0bI0HEzLhbNGtdC6ttRMWC21YGihkEaDQgCBQjEnK2htW6zLtSrklNz83ULwMQZ0zRC2Oxv2DWfNsc9h--bYR_4CQMZZYA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Molecular architecture of KedS8, a sugar N ‐methyltransferase from S treptoalloteichus sp. ATCC 53650</title><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Wiley Free Content</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Delvaux, Nathan A. ; Thoden, James B. ; Holden, Hazel M.</creator><creatorcontrib>Delvaux, Nathan A. ; Thoden, James B. ; Holden, Hazel M.</creatorcontrib><description>Kedarcidin, produced by Streptoalloteichus sp. ATCC 53650, is a fascinating chromoprotein of 114 amino acid residues that displays both antibiotic and anticancer activity. The chromophore responsible for its chemotherapeutic activity is an ansa‐bridged enediyne with two attached sugars, l ‐mycarose, and l ‐kedarosamine. The biosynthesis of l ‐kedarosamine, a highly unusual trideoxysugar, is beginning to be revealed through bioinformatics approaches. One of the enzymes putatively involved in the production of this carbohydrate is referred to as KedS8. It has been proposed that KedS8 is an N ‐methyltransferase that utilizes S ‐adenosylmethionine as the methyl donor and a dTDP‐linked C‐4′ amino sugar as the substrate. Here we describe the three‐dimensional architecture of KedS8 in complex with S ‐adenosylhomocysteine. The structure was solved to 2.0 Å resolution and refined to an overall R ‐factor of 17.1%. Unlike that observed for other sugar N ‐methyltransferases, KedS8 adopts a novel tetrameric quaternary structure due to the swapping of β‐strands at the N‐termini of its subunits. The structure presented here represents the first example of an N ‐methyltransferase that functions on C‐4′ rather than C‐3′ amino sugars.</description><identifier>ISSN: 0961-8368</identifier><identifier>EISSN: 1469-896X</identifier><identifier>DOI: 10.1002/pro.2742</identifier><language>eng</language><ispartof>Protein science, 2015-10, Vol.24 (10), p.1593-1599</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c722-383c963791c9b12fa94bcbfb7602a63620eac5396c4ecc2e240f38cbab5d7d453</citedby><cites>FETCH-LOGICAL-c722-383c963791c9b12fa94bcbfb7602a63620eac5396c4ecc2e240f38cbab5d7d453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Delvaux, Nathan A.</creatorcontrib><creatorcontrib>Thoden, James B.</creatorcontrib><creatorcontrib>Holden, Hazel M.</creatorcontrib><title>Molecular architecture of KedS8, a sugar N ‐methyltransferase from S treptoalloteichus sp. ATCC 53650</title><title>Protein science</title><description>Kedarcidin, produced by Streptoalloteichus sp. ATCC 53650, is a fascinating chromoprotein of 114 amino acid residues that displays both antibiotic and anticancer activity. The chromophore responsible for its chemotherapeutic activity is an ansa‐bridged enediyne with two attached sugars, l ‐mycarose, and l ‐kedarosamine. The biosynthesis of l ‐kedarosamine, a highly unusual trideoxysugar, is beginning to be revealed through bioinformatics approaches. One of the enzymes putatively involved in the production of this carbohydrate is referred to as KedS8. It has been proposed that KedS8 is an N ‐methyltransferase that utilizes S ‐adenosylmethionine as the methyl donor and a dTDP‐linked C‐4′ amino sugar as the substrate. Here we describe the three‐dimensional architecture of KedS8 in complex with S ‐adenosylhomocysteine. The structure was solved to 2.0 Å resolution and refined to an overall R ‐factor of 17.1%. Unlike that observed for other sugar N ‐methyltransferases, KedS8 adopts a novel tetrameric quaternary structure due to the swapping of β‐strands at the N‐termini of its subunits. The structure presented here represents the first example of an N ‐methyltransferase that functions on C‐4′ rather than C‐3′ amino sugars.</description><issn>0961-8368</issn><issn>1469-896X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNotkL1OwzAURi0EEqUg8QgeGUjwX5x4rCIoiAJDO7BFzu11U5TiyHaGbjwCz8iT0Aqmo09H-oZDyDVnOWdM3A3B56JU4oRMuNImq4x-PyUTZjTPKqmrc3IR4wdjTHEhJ2Tz4nuEsbeB2gDdNiGkMSD1jj7jelndUkvjuDnoV_rz9b3D1O37FOxndBhsROqC39ElTQGH5G3f-4Rb6MZI45DT2aquaSF1wS7JmbN9xKt_Tsnq4X5VP2aLt_lTPVtkUAqRyUqC0bI0HEzLhbNGtdC6ttRMWC21YGihkEaDQgCBQjEnK2htW6zLtSrklNz83ULwMQZ0zRC2Oxv2DWfNsc9h--bYR_4CQMZZYA</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Delvaux, Nathan A.</creator><creator>Thoden, James B.</creator><creator>Holden, Hazel M.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201510</creationdate><title>Molecular architecture of KedS8, a sugar N ‐methyltransferase from S treptoalloteichus sp. ATCC 53650</title><author>Delvaux, Nathan A. ; Thoden, James B. ; Holden, Hazel M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c722-383c963791c9b12fa94bcbfb7602a63620eac5396c4ecc2e240f38cbab5d7d453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Delvaux, Nathan A.</creatorcontrib><creatorcontrib>Thoden, James B.</creatorcontrib><creatorcontrib>Holden, Hazel M.</creatorcontrib><collection>CrossRef</collection><jtitle>Protein science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Delvaux, Nathan A.</au><au>Thoden, James B.</au><au>Holden, Hazel M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular architecture of KedS8, a sugar N ‐methyltransferase from S treptoalloteichus sp. ATCC 53650</atitle><jtitle>Protein science</jtitle><date>2015-10</date><risdate>2015</risdate><volume>24</volume><issue>10</issue><spage>1593</spage><epage>1599</epage><pages>1593-1599</pages><issn>0961-8368</issn><eissn>1469-896X</eissn><abstract>Kedarcidin, produced by Streptoalloteichus sp. ATCC 53650, is a fascinating chromoprotein of 114 amino acid residues that displays both antibiotic and anticancer activity. The chromophore responsible for its chemotherapeutic activity is an ansa‐bridged enediyne with two attached sugars, l ‐mycarose, and l ‐kedarosamine. The biosynthesis of l ‐kedarosamine, a highly unusual trideoxysugar, is beginning to be revealed through bioinformatics approaches. One of the enzymes putatively involved in the production of this carbohydrate is referred to as KedS8. It has been proposed that KedS8 is an N ‐methyltransferase that utilizes S ‐adenosylmethionine as the methyl donor and a dTDP‐linked C‐4′ amino sugar as the substrate. Here we describe the three‐dimensional architecture of KedS8 in complex with S ‐adenosylhomocysteine. The structure was solved to 2.0 Å resolution and refined to an overall R ‐factor of 17.1%. Unlike that observed for other sugar N ‐methyltransferases, KedS8 adopts a novel tetrameric quaternary structure due to the swapping of β‐strands at the N‐termini of its subunits. The structure presented here represents the first example of an N ‐methyltransferase that functions on C‐4′ rather than C‐3′ amino sugars.</abstract><doi>10.1002/pro.2742</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0961-8368
ispartof Protein science, 2015-10, Vol.24 (10), p.1593-1599
issn 0961-8368
1469-896X
language eng
recordid cdi_crossref_primary_10_1002_pro_2742
source Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; PubMed Central; Free Full-Text Journals in Chemistry
title Molecular architecture of KedS8, a sugar N ‐methyltransferase from S treptoalloteichus sp. ATCC 53650
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T00%3A44%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20architecture%20of%20KedS8,%20a%20sugar%20N%20%E2%80%90methyltransferase%20from%20S%20treptoalloteichus%20sp.%20ATCC%2053650&rft.jtitle=Protein%20science&rft.au=Delvaux,%20Nathan%20A.&rft.date=2015-10&rft.volume=24&rft.issue=10&rft.spage=1593&rft.epage=1599&rft.pages=1593-1599&rft.issn=0961-8368&rft.eissn=1469-896X&rft_id=info:doi/10.1002/pro.2742&rft_dat=%3Ccrossref%3E10_1002_pro_2742%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true