Fungal Ice2p is in the same superfamily as SERINCs, restriction factors for HIV and other viruses
Ice2p is an integral endoplasmic reticulum (ER) membrane protein in budding yeast S. cerevisiae named ICE because it is required for Inheritance of Cortical ER. Ice2p has also been reported to be involved in an ER metabolic branch‐point that regulates the flux of lipid either to be stored in lipid d...
Gespeichert in:
Veröffentlicht in: | Proteins, structure, function, and bioinformatics structure, function, and bioinformatics, 2021-10, Vol.89 (10), p.1240-1250 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1250 |
---|---|
container_issue | 10 |
container_start_page | 1240 |
container_title | Proteins, structure, function, and bioinformatics |
container_volume | 89 |
creator | Alli‐Balogun, Ganiyu O. Levine, Tim P. |
description | Ice2p is an integral endoplasmic reticulum (ER) membrane protein in budding yeast S. cerevisiae named ICE because it is required for Inheritance of Cortical ER. Ice2p has also been reported to be involved in an ER metabolic branch‐point that regulates the flux of lipid either to be stored in lipid droplets or to be used as membrane components. Alternately, Ice2p has been proposed to act as a tether that physically bridges the ER at contact sites with both lipid droplets and the plasma membrane via a long loop on the protein's cytoplasmic face that contains multiple predicted amphipathic helices. Here we carried out a bioinformatic analysis to increase understanding of Ice2p. First, regarding topology, we found that diverse members of the fungal Ice2 family have 10 transmembrane helices (TMHs), which places the long loop on the exofacial face of Ice2p, where it cannot form inter‐organelle bridges. Second, we identified Ice2p as a full‐length homolog of SERINC (serine incorporator), a family of proteins with 10 TMHs found universally in eukaryotes. Since SERINCs are potent restriction factors for HIV and other viruses, study of Ice2p may reveal functions or mechanisms that shed light on viral restriction by SERINCs. |
doi_str_mv | 10.1002/prot.26145 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2526306807</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2526306807</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3935-5b962407d9a93042457a9e62d889543c3e26ce8c8aeeb7a5a49cc8cc92dad9853</originalsourceid><addsrcrecordid>eNp9kE9LwzAYh4Mobk4vfgAJeBGxM02aNDnK2FxhOJnTa8nSVDP6Zyatsm9vZqcHD17e9_Lw8OMB4DxEwxAhfLuxdTPELIzoAeiHSMQBCkl0CPqI8zgglNMeOHFujRBigrBj0CNEcEww6wM5aatXWcBEabyBxkFTweZNQydLf9qNtrksTbGF0sGn8SJ5GLkbaLVrrFGNqSuYS9XU1sG8tnCavEBZZbD2Bgs_jG2ddqfgKJeF02f7PwDPk_FyNA1m8_tkdDcLFBGEBnQlGI5QnAkpCIpwRGMpNMMZ54JGRBGNmdJccan1KpZURkIprpTAmcwEp2QArjqvz_He-oVpaZzSRSErXbcuxRQzghhHsUcv_6DrurWVX-cpJlDIoph76rqjlK2dszpPN9aU0m7TEKW78OkufPod3sMXe2W7KnX2i_6U9kDYAZ-m0Nt_VOnjYr7spF_GAoyB</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2569016478</pqid></control><display><type>article</type><title>Fungal Ice2p is in the same superfamily as SERINCs, restriction factors for HIV and other viruses</title><source>MEDLINE</source><source>Wiley Journals</source><creator>Alli‐Balogun, Ganiyu O. ; Levine, Tim P.</creator><creatorcontrib>Alli‐Balogun, Ganiyu O. ; Levine, Tim P.</creatorcontrib><description>Ice2p is an integral endoplasmic reticulum (ER) membrane protein in budding yeast S. cerevisiae named ICE because it is required for Inheritance of Cortical ER. Ice2p has also been reported to be involved in an ER metabolic branch‐point that regulates the flux of lipid either to be stored in lipid droplets or to be used as membrane components. Alternately, Ice2p has been proposed to act as a tether that physically bridges the ER at contact sites with both lipid droplets and the plasma membrane via a long loop on the protein's cytoplasmic face that contains multiple predicted amphipathic helices. Here we carried out a bioinformatic analysis to increase understanding of Ice2p. First, regarding topology, we found that diverse members of the fungal Ice2 family have 10 transmembrane helices (TMHs), which places the long loop on the exofacial face of Ice2p, where it cannot form inter‐organelle bridges. Second, we identified Ice2p as a full‐length homolog of SERINC (serine incorporator), a family of proteins with 10 TMHs found universally in eukaryotes. Since SERINCs are potent restriction factors for HIV and other viruses, study of Ice2p may reveal functions or mechanisms that shed light on viral restriction by SERINCs.</description><identifier>ISSN: 0887-3585</identifier><identifier>EISSN: 1097-0134</identifier><identifier>DOI: 10.1002/prot.26145</identifier><identifier>PMID: 33982326</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Bridges ; Cell Membrane - metabolism ; Droplets ; Endoplasmic reticulum ; Endoplasmic Reticulum - metabolism ; Eukaryotes ; Fungi ; Helices ; HIV ; Homology ; Human immunodeficiency virus ; Ice2p ; Lipids ; membrane contact site ; Membrane proteins ; Membrane Proteins - chemistry ; Membranes ; Protein Structure, Secondary ; Proteins ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae Proteins - chemistry ; SERINC ; Serine ; tether ; Topology ; virus restriction factor ; Viruses ; Yeasts</subject><ispartof>Proteins, structure, function, and bioinformatics, 2021-10, Vol.89 (10), p.1240-1250</ispartof><rights>2021 The Authors. published by Wiley Periodicals LLC.</rights><rights>2021 The Authors. Proteins: Structure, Function, and Bioinformatics published by Wiley Periodicals LLC.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3935-5b962407d9a93042457a9e62d889543c3e26ce8c8aeeb7a5a49cc8cc92dad9853</citedby><cites>FETCH-LOGICAL-c3935-5b962407d9a93042457a9e62d889543c3e26ce8c8aeeb7a5a49cc8cc92dad9853</cites><orcidid>0000-0002-7231-0775 ; 0000-0002-1027-6356</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fprot.26145$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fprot.26145$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33982326$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alli‐Balogun, Ganiyu O.</creatorcontrib><creatorcontrib>Levine, Tim P.</creatorcontrib><title>Fungal Ice2p is in the same superfamily as SERINCs, restriction factors for HIV and other viruses</title><title>Proteins, structure, function, and bioinformatics</title><addtitle>Proteins</addtitle><description>Ice2p is an integral endoplasmic reticulum (ER) membrane protein in budding yeast S. cerevisiae named ICE because it is required for Inheritance of Cortical ER. Ice2p has also been reported to be involved in an ER metabolic branch‐point that regulates the flux of lipid either to be stored in lipid droplets or to be used as membrane components. Alternately, Ice2p has been proposed to act as a tether that physically bridges the ER at contact sites with both lipid droplets and the plasma membrane via a long loop on the protein's cytoplasmic face that contains multiple predicted amphipathic helices. Here we carried out a bioinformatic analysis to increase understanding of Ice2p. First, regarding topology, we found that diverse members of the fungal Ice2 family have 10 transmembrane helices (TMHs), which places the long loop on the exofacial face of Ice2p, where it cannot form inter‐organelle bridges. Second, we identified Ice2p as a full‐length homolog of SERINC (serine incorporator), a family of proteins with 10 TMHs found universally in eukaryotes. Since SERINCs are potent restriction factors for HIV and other viruses, study of Ice2p may reveal functions or mechanisms that shed light on viral restriction by SERINCs.</description><subject>Bridges</subject><subject>Cell Membrane - metabolism</subject><subject>Droplets</subject><subject>Endoplasmic reticulum</subject><subject>Endoplasmic Reticulum - metabolism</subject><subject>Eukaryotes</subject><subject>Fungi</subject><subject>Helices</subject><subject>HIV</subject><subject>Homology</subject><subject>Human immunodeficiency virus</subject><subject>Ice2p</subject><subject>Lipids</subject><subject>membrane contact site</subject><subject>Membrane proteins</subject><subject>Membrane Proteins - chemistry</subject><subject>Membranes</subject><subject>Protein Structure, Secondary</subject><subject>Proteins</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae Proteins - chemistry</subject><subject>SERINC</subject><subject>Serine</subject><subject>tether</subject><subject>Topology</subject><subject>virus restriction factor</subject><subject>Viruses</subject><subject>Yeasts</subject><issn>0887-3585</issn><issn>1097-0134</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp9kE9LwzAYh4Mobk4vfgAJeBGxM02aNDnK2FxhOJnTa8nSVDP6Zyatsm9vZqcHD17e9_Lw8OMB4DxEwxAhfLuxdTPELIzoAeiHSMQBCkl0CPqI8zgglNMeOHFujRBigrBj0CNEcEww6wM5aatXWcBEabyBxkFTweZNQydLf9qNtrksTbGF0sGn8SJ5GLkbaLVrrFGNqSuYS9XU1sG8tnCavEBZZbD2Bgs_jG2ddqfgKJeF02f7PwDPk_FyNA1m8_tkdDcLFBGEBnQlGI5QnAkpCIpwRGMpNMMZ54JGRBGNmdJccan1KpZURkIprpTAmcwEp2QArjqvz_He-oVpaZzSRSErXbcuxRQzghhHsUcv_6DrurWVX-cpJlDIoph76rqjlK2dszpPN9aU0m7TEKW78OkufPod3sMXe2W7KnX2i_6U9kDYAZ-m0Nt_VOnjYr7spF_GAoyB</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Alli‐Balogun, Ganiyu O.</creator><creator>Levine, Tim P.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</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>7QO</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>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7231-0775</orcidid><orcidid>https://orcid.org/0000-0002-1027-6356</orcidid></search><sort><creationdate>202110</creationdate><title>Fungal Ice2p is in the same superfamily as SERINCs, restriction factors for HIV and other viruses</title><author>Alli‐Balogun, Ganiyu O. ; Levine, Tim P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3935-5b962407d9a93042457a9e62d889543c3e26ce8c8aeeb7a5a49cc8cc92dad9853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Bridges</topic><topic>Cell Membrane - metabolism</topic><topic>Droplets</topic><topic>Endoplasmic reticulum</topic><topic>Endoplasmic Reticulum - metabolism</topic><topic>Eukaryotes</topic><topic>Fungi</topic><topic>Helices</topic><topic>HIV</topic><topic>Homology</topic><topic>Human immunodeficiency virus</topic><topic>Ice2p</topic><topic>Lipids</topic><topic>membrane contact site</topic><topic>Membrane proteins</topic><topic>Membrane Proteins - chemistry</topic><topic>Membranes</topic><topic>Protein Structure, Secondary</topic><topic>Proteins</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae Proteins - chemistry</topic><topic>SERINC</topic><topic>Serine</topic><topic>tether</topic><topic>Topology</topic><topic>virus restriction factor</topic><topic>Viruses</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alli‐Balogun, Ganiyu O.</creatorcontrib><creatorcontrib>Levine, Tim P.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</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>Biotechnology Research Abstracts</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Proteins, structure, function, and bioinformatics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alli‐Balogun, Ganiyu O.</au><au>Levine, Tim P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fungal Ice2p is in the same superfamily as SERINCs, restriction factors for HIV and other viruses</atitle><jtitle>Proteins, structure, function, and bioinformatics</jtitle><addtitle>Proteins</addtitle><date>2021-10</date><risdate>2021</risdate><volume>89</volume><issue>10</issue><spage>1240</spage><epage>1250</epage><pages>1240-1250</pages><issn>0887-3585</issn><eissn>1097-0134</eissn><abstract>Ice2p is an integral endoplasmic reticulum (ER) membrane protein in budding yeast S. cerevisiae named ICE because it is required for Inheritance of Cortical ER. Ice2p has also been reported to be involved in an ER metabolic branch‐point that regulates the flux of lipid either to be stored in lipid droplets or to be used as membrane components. Alternately, Ice2p has been proposed to act as a tether that physically bridges the ER at contact sites with both lipid droplets and the plasma membrane via a long loop on the protein's cytoplasmic face that contains multiple predicted amphipathic helices. Here we carried out a bioinformatic analysis to increase understanding of Ice2p. First, regarding topology, we found that diverse members of the fungal Ice2 family have 10 transmembrane helices (TMHs), which places the long loop on the exofacial face of Ice2p, where it cannot form inter‐organelle bridges. Second, we identified Ice2p as a full‐length homolog of SERINC (serine incorporator), a family of proteins with 10 TMHs found universally in eukaryotes. Since SERINCs are potent restriction factors for HIV and other viruses, study of Ice2p may reveal functions or mechanisms that shed light on viral restriction by SERINCs.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>33982326</pmid><doi>10.1002/prot.26145</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7231-0775</orcidid><orcidid>https://orcid.org/0000-0002-1027-6356</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0887-3585 |
ispartof | Proteins, structure, function, and bioinformatics, 2021-10, Vol.89 (10), p.1240-1250 |
issn | 0887-3585 1097-0134 |
language | eng |
recordid | cdi_proquest_miscellaneous_2526306807 |
source | MEDLINE; Wiley Journals |
subjects | Bridges Cell Membrane - metabolism Droplets Endoplasmic reticulum Endoplasmic Reticulum - metabolism Eukaryotes Fungi Helices HIV Homology Human immunodeficiency virus Ice2p Lipids membrane contact site Membrane proteins Membrane Proteins - chemistry Membranes Protein Structure, Secondary Proteins Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae Proteins - chemistry SERINC Serine tether Topology virus restriction factor Viruses Yeasts |
title | Fungal Ice2p is in the same superfamily as SERINCs, restriction factors for HIV and other viruses |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T15%3A02%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Fungal%20Ice2p%20is%20in%20the%20same%20superfamily%20as%20SERINCs,%20restriction%20factors%20for%20HIV%20and%20other%20viruses&rft.jtitle=Proteins,%20structure,%20function,%20and%20bioinformatics&rft.au=Alli%E2%80%90Balogun,%20Ganiyu%20O.&rft.date=2021-10&rft.volume=89&rft.issue=10&rft.spage=1240&rft.epage=1250&rft.pages=1240-1250&rft.issn=0887-3585&rft.eissn=1097-0134&rft_id=info:doi/10.1002/prot.26145&rft_dat=%3Cproquest_cross%3E2526306807%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2569016478&rft_id=info:pmid/33982326&rfr_iscdi=true |