MOESM2 of Replacement of feline foamy virus bet by feline immunodeficiency virus vif yields replicative virus with novel vaccine candidate potential
Additional file 2. Partial genome sequences from pCF7-Vif-4 and the stop mutations of the in vitro-selected FFV-Vif variants. The Trp codon and the downstream G residue (TGGG) ~ 130 bp upstream of the vif coding sequence are in bold face letters and underlined. In pCF7-Vif W/*1 (in blue), the mutati...
Gespeichert in:
Hauptverfasser: | , , , , , , , , , , , , |
---|---|
Format: | Bild |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | Ledesma-Feliciano, Carmen Hagen, Sarah Troyer, Ryan Zheng, Xin Musselman, Esther Slavkovic Lukic, Dragana Franke, Ann-Mareen Maeda, Daniel Zielonka, Jörg Münk, Carsten Wei, Guochao VandeWoude, Sue Löchelt, Martin |
description | Additional file 2. Partial genome sequences from pCF7-Vif-4 and the stop mutations of the in vitro-selected FFV-Vif variants. The Trp codon and the downstream G residue (TGGG) ~ 130 bp upstream of the vif coding sequence are in bold face letters and underlined. In pCF7-Vif W/*1 (in blue), the mutation is from TGG to TGA and for mutant W/*2 (in green) the mutation is from TGGG to TAGA, with both mutations resulting in a Trp (W) to Stop (*) mutation (W/*) as indicated. The bet nucleotide sequence is in black, the linker sequence in pink with recognition sites for NheI (in brown) and SacII (in light violet). The vif gene is marked in blue with the authentic Met start codon in bold. The BettrVif fusion protein is highlighted in yellow with the amino acids color-coded as described above for the genes. The Met residue 14 amino acids upstream of the authentic vif start codon is highlighted in bold and underlining. The C-terminal amino acid sequence of tas is highlighted in red. |
doi_str_mv | 10.6084/m9.figshare.6279725 |
format | Image |
fullrecord | <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_6084_m9_figshare_6279725</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_6084_m9_figshare_6279725</sourcerecordid><originalsourceid>FETCH-datacite_primary_10_6084_m9_figshare_62797253</originalsourceid><addsrcrecordid>eNqdj0tuwkAQRGfDIgJOkE1fAGPM12sEygYhJdmPmnEPtDQfazxM5HtwYGzJvkBWpVZVV-kJ8bnKs11-2CxtmWm-Nw8MlO2Kfbkvth_idbmefi4FeA3fVBtUZMnF_tRk2BFoj7aFxOHZwI0i3NrRYWufzlekWTE5NYYSa2iZTNVA6BpZYeREg_nH8QHOJzKQUKm-RqGruMJIUPvYbTOamZhoNA3NB52K9fn0e_xadDFUHEnWgS2GVq5y2bNJW8qRTQ5s6_99vQG0mmXC</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>image</recordtype></control><display><type>image</type><title>MOESM2 of Replacement of feline foamy virus bet by feline immunodeficiency virus vif yields replicative virus with novel vaccine candidate potential</title><source>DataCite</source><creator>Ledesma-Feliciano, Carmen ; Hagen, Sarah ; Troyer, Ryan ; Zheng, Xin ; Musselman, Esther ; Slavkovic Lukic, Dragana ; Franke, Ann-Mareen ; Maeda, Daniel ; Zielonka, Jörg ; Münk, Carsten ; Wei, Guochao ; VandeWoude, Sue ; Löchelt, Martin</creator><creatorcontrib>Ledesma-Feliciano, Carmen ; Hagen, Sarah ; Troyer, Ryan ; Zheng, Xin ; Musselman, Esther ; Slavkovic Lukic, Dragana ; Franke, Ann-Mareen ; Maeda, Daniel ; Zielonka, Jörg ; Münk, Carsten ; Wei, Guochao ; VandeWoude, Sue ; Löchelt, Martin</creatorcontrib><description>Additional file 2. Partial genome sequences from pCF7-Vif-4 and the stop mutations of the in vitro-selected FFV-Vif variants. The Trp codon and the downstream G residue (TGGG) ~ 130 bp upstream of the vif coding sequence are in bold face letters and underlined. In pCF7-Vif W/*1 (in blue), the mutation is from TGG to TGA and for mutant W/*2 (in green) the mutation is from TGGG to TAGA, with both mutations resulting in a Trp (W) to Stop (*) mutation (W/*) as indicated. The bet nucleotide sequence is in black, the linker sequence in pink with recognition sites for NheI (in brown) and SacII (in light violet). The vif gene is marked in blue with the authentic Met start codon in bold. The BettrVif fusion protein is highlighted in yellow with the amino acids color-coded as described above for the genes. The Met residue 14 amino acids upstream of the authentic vif start codon is highlighted in bold and underlining. The C-terminal amino acid sequence of tas is highlighted in red.</description><identifier>DOI: 10.6084/m9.figshare.6279725</identifier><language>eng</language><publisher>figshare</publisher><subject>Biological Sciences not elsewhere classified ; Biotechnology ; Evolutionary Biology ; FOS: Biological sciences ; FOS: Clinical medicine ; FOS: Health sciences ; Genetics ; Immunology ; Infectious Diseases ; Information Systems not elsewhere classified ; Medicine ; Microbiology ; Molecular Biology ; Plant Biology ; Virology</subject><creationdate>2018</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1888</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.6279725$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Ledesma-Feliciano, Carmen</creatorcontrib><creatorcontrib>Hagen, Sarah</creatorcontrib><creatorcontrib>Troyer, Ryan</creatorcontrib><creatorcontrib>Zheng, Xin</creatorcontrib><creatorcontrib>Musselman, Esther</creatorcontrib><creatorcontrib>Slavkovic Lukic, Dragana</creatorcontrib><creatorcontrib>Franke, Ann-Mareen</creatorcontrib><creatorcontrib>Maeda, Daniel</creatorcontrib><creatorcontrib>Zielonka, Jörg</creatorcontrib><creatorcontrib>Münk, Carsten</creatorcontrib><creatorcontrib>Wei, Guochao</creatorcontrib><creatorcontrib>VandeWoude, Sue</creatorcontrib><creatorcontrib>Löchelt, Martin</creatorcontrib><title>MOESM2 of Replacement of feline foamy virus bet by feline immunodeficiency virus vif yields replicative virus with novel vaccine candidate potential</title><description>Additional file 2. Partial genome sequences from pCF7-Vif-4 and the stop mutations of the in vitro-selected FFV-Vif variants. The Trp codon and the downstream G residue (TGGG) ~ 130 bp upstream of the vif coding sequence are in bold face letters and underlined. In pCF7-Vif W/*1 (in blue), the mutation is from TGG to TGA and for mutant W/*2 (in green) the mutation is from TGGG to TAGA, with both mutations resulting in a Trp (W) to Stop (*) mutation (W/*) as indicated. The bet nucleotide sequence is in black, the linker sequence in pink with recognition sites for NheI (in brown) and SacII (in light violet). The vif gene is marked in blue with the authentic Met start codon in bold. The BettrVif fusion protein is highlighted in yellow with the amino acids color-coded as described above for the genes. The Met residue 14 amino acids upstream of the authentic vif start codon is highlighted in bold and underlining. The C-terminal amino acid sequence of tas is highlighted in red.</description><subject>Biological Sciences not elsewhere classified</subject><subject>Biotechnology</subject><subject>Evolutionary Biology</subject><subject>FOS: Biological sciences</subject><subject>FOS: Clinical medicine</subject><subject>FOS: Health sciences</subject><subject>Genetics</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Information Systems not elsewhere classified</subject><subject>Medicine</subject><subject>Microbiology</subject><subject>Molecular Biology</subject><subject>Plant Biology</subject><subject>Virology</subject><fulltext>true</fulltext><rsrctype>image</rsrctype><creationdate>2018</creationdate><recordtype>image</recordtype><sourceid>PQ8</sourceid><recordid>eNqdj0tuwkAQRGfDIgJOkE1fAGPM12sEygYhJdmPmnEPtDQfazxM5HtwYGzJvkBWpVZVV-kJ8bnKs11-2CxtmWm-Nw8MlO2Kfbkvth_idbmefi4FeA3fVBtUZMnF_tRk2BFoj7aFxOHZwI0i3NrRYWufzlekWTE5NYYSa2iZTNVA6BpZYeREg_nH8QHOJzKQUKm-RqGruMJIUPvYbTOamZhoNA3NB52K9fn0e_xadDFUHEnWgS2GVq5y2bNJW8qRTQ5s6_99vQG0mmXC</recordid><startdate>20180517</startdate><enddate>20180517</enddate><creator>Ledesma-Feliciano, Carmen</creator><creator>Hagen, Sarah</creator><creator>Troyer, Ryan</creator><creator>Zheng, Xin</creator><creator>Musselman, Esther</creator><creator>Slavkovic Lukic, Dragana</creator><creator>Franke, Ann-Mareen</creator><creator>Maeda, Daniel</creator><creator>Zielonka, Jörg</creator><creator>Münk, Carsten</creator><creator>Wei, Guochao</creator><creator>VandeWoude, Sue</creator><creator>Löchelt, Martin</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20180517</creationdate><title>MOESM2 of Replacement of feline foamy virus bet by feline immunodeficiency virus vif yields replicative virus with novel vaccine candidate potential</title><author>Ledesma-Feliciano, Carmen ; Hagen, Sarah ; Troyer, Ryan ; Zheng, Xin ; Musselman, Esther ; Slavkovic Lukic, Dragana ; Franke, Ann-Mareen ; Maeda, Daniel ; Zielonka, Jörg ; Münk, Carsten ; Wei, Guochao ; VandeWoude, Sue ; Löchelt, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_62797253</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Biological Sciences not elsewhere classified</topic><topic>Biotechnology</topic><topic>Evolutionary Biology</topic><topic>FOS: Biological sciences</topic><topic>FOS: Clinical medicine</topic><topic>FOS: Health sciences</topic><topic>Genetics</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><topic>Information Systems not elsewhere classified</topic><topic>Medicine</topic><topic>Microbiology</topic><topic>Molecular Biology</topic><topic>Plant Biology</topic><topic>Virology</topic><toplevel>online_resources</toplevel><creatorcontrib>Ledesma-Feliciano, Carmen</creatorcontrib><creatorcontrib>Hagen, Sarah</creatorcontrib><creatorcontrib>Troyer, Ryan</creatorcontrib><creatorcontrib>Zheng, Xin</creatorcontrib><creatorcontrib>Musselman, Esther</creatorcontrib><creatorcontrib>Slavkovic Lukic, Dragana</creatorcontrib><creatorcontrib>Franke, Ann-Mareen</creatorcontrib><creatorcontrib>Maeda, Daniel</creatorcontrib><creatorcontrib>Zielonka, Jörg</creatorcontrib><creatorcontrib>Münk, Carsten</creatorcontrib><creatorcontrib>Wei, Guochao</creatorcontrib><creatorcontrib>VandeWoude, Sue</creatorcontrib><creatorcontrib>Löchelt, Martin</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Ledesma-Feliciano, Carmen</au><au>Hagen, Sarah</au><au>Troyer, Ryan</au><au>Zheng, Xin</au><au>Musselman, Esther</au><au>Slavkovic Lukic, Dragana</au><au>Franke, Ann-Mareen</au><au>Maeda, Daniel</au><au>Zielonka, Jörg</au><au>Münk, Carsten</au><au>Wei, Guochao</au><au>VandeWoude, Sue</au><au>Löchelt, Martin</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>MOESM2 of Replacement of feline foamy virus bet by feline immunodeficiency virus vif yields replicative virus with novel vaccine candidate potential</title><date>2018-05-17</date><risdate>2018</risdate><abstract>Additional file 2. Partial genome sequences from pCF7-Vif-4 and the stop mutations of the in vitro-selected FFV-Vif variants. The Trp codon and the downstream G residue (TGGG) ~ 130 bp upstream of the vif coding sequence are in bold face letters and underlined. In pCF7-Vif W/*1 (in blue), the mutation is from TGG to TGA and for mutant W/*2 (in green) the mutation is from TGGG to TAGA, with both mutations resulting in a Trp (W) to Stop (*) mutation (W/*) as indicated. The bet nucleotide sequence is in black, the linker sequence in pink with recognition sites for NheI (in brown) and SacII (in light violet). The vif gene is marked in blue with the authentic Met start codon in bold. The BettrVif fusion protein is highlighted in yellow with the amino acids color-coded as described above for the genes. The Met residue 14 amino acids upstream of the authentic vif start codon is highlighted in bold and underlining. The C-terminal amino acid sequence of tas is highlighted in red.</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.6279725</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | DOI: 10.6084/m9.figshare.6279725 |
ispartof | |
issn | |
language | eng |
recordid | cdi_datacite_primary_10_6084_m9_figshare_6279725 |
source | DataCite |
subjects | Biological Sciences not elsewhere classified Biotechnology Evolutionary Biology FOS: Biological sciences FOS: Clinical medicine FOS: Health sciences Genetics Immunology Infectious Diseases Information Systems not elsewhere classified Medicine Microbiology Molecular Biology Plant Biology Virology |
title | MOESM2 of Replacement of feline foamy virus bet by feline immunodeficiency virus vif yields replicative virus with novel vaccine candidate potential |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T03%3A09%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Ledesma-Feliciano,%20Carmen&rft.date=2018-05-17&rft_id=info:doi/10.6084/m9.figshare.6279725&rft_dat=%3Cdatacite_PQ8%3E10_6084_m9_figshare_6279725%3C/datacite_PQ8%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 |