Molecular characterization of the E2 conjugating enzyme LinfUbc13 in Leishmania infantum

UBC13 is an orthologue of Homo sapiens ubiquitin-conjugation E2 enzymes described in Leishmania mexicana, a null mutant lacking this gene cannot be produced, suggesting essential functions in this parasite. Leishmania infantum is an etiological agent of visceral leishmaniasis, the most severe type o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Archives of biochemistry and biophysics 2025-02, Vol.764, p.110272, Article 110272
Hauptverfasser: Rodrigues da Silva, Eduardo Vagner, Torres, Caroline, Nemamiah Escolarique Ribeiro, Hariel, Santana Travaglini Berti de Correia, Camila Rolemberg, de Oliveira de Castro, Taissa, da Costa Mancin, Giovanna, Zanchetta Venancio, Mayla Gabriela, Abdel Baqui, Munira Muhammad, Teixeira, Felipe Roberti, Gomes, Marcelo Damário
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page 110272
container_title Archives of biochemistry and biophysics
container_volume 764
creator Rodrigues da Silva, Eduardo Vagner
Torres, Caroline
Nemamiah Escolarique Ribeiro, Hariel
Santana Travaglini Berti de Correia, Camila Rolemberg
de Oliveira de Castro, Taissa
da Costa Mancin, Giovanna
Zanchetta Venancio, Mayla Gabriela
Abdel Baqui, Munira Muhammad
Teixeira, Felipe Roberti
Gomes, Marcelo Damário
description UBC13 is an orthologue of Homo sapiens ubiquitin-conjugation E2 enzymes described in Leishmania mexicana, a null mutant lacking this gene cannot be produced, suggesting essential functions in this parasite. Leishmania infantum is an etiological agent of visceral leishmaniasis, the most severe type of disease that is potentially fatal if untreated. The ubiquitination process has been targeted for leishmanicidal compounds, indicating its essential function in parasite homeostasis. Therefore, the molecular characterization of the ubiquitination process may provide a better understanding of the molecular and cellular basis of leishmaniasis. Here, we characterized the gene LINF_350017900 in Leishmania infantum, which was named LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3. LinfUbc13 contains conserved catalytic residues, including Cys86 and the HPN motif, which are essential for ubiquitin-conjugating activity. Structural analysis revealed a high similarity between LinfUbc13 and human UBE2D proteins, with a root-mean-square deviation (RMSD) of 0.4 Å, suggesting conserved functions. Recombinant LinfUbc13 was expressed and shown to accept ubiquitin from E1, forming a thioester intermediate. Functional assays demonstrated that LinfUbc13 transfers ubiquitin to p53 through human HDM2 E3 ligase, confirming its role in ubiquitination. Subcellular localization showed that LinfUbc13 was distributed throughout the parasite cytoplasm. These findings highlight the conserved nature of the ubiquitin-proteasome system between Leishmania infantum and Homo sapiens, showing that LinfUbc13 is an E2 enzyme that plays a crucial role in parasitic development. [Display omitted] •LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3.•Recombinant LinfUbc13 is able to accept ubiquitin from E1, forming a thioester intermediate.•LinfUbc13 is present in the cytosol of parasites.•LinfUbc13 is an essential gene.
doi_str_mv 10.1016/j.abb.2024.110272
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3146948394</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0003986124003941</els_id><sourcerecordid>3146948394</sourcerecordid><originalsourceid>FETCH-LOGICAL-c235t-ff4c8405c73d95c2bf0d97f1af5fb44785ebcdc1933bbc19539ba9e6fbd0a5053</originalsourceid><addsrcrecordid>eNp9kE9LxDAQxYMouq5-AC-So5euSZO0DZ5E_AcrXlzwFpJ04mZpU01aQT-9kVWPnoYZ3nvD-yF0QsmCElqdbxbamEVJSr6glJR1uYNmlMiqIKzhu2hGCGGFbCp6gA5T2hBCKa_KfXTAZNXIWtAZen4YOrBTpyO2ax21HSH6Tz36IeDB4XEN-LrEdgib6SVfwwuG8PnRA1764FbGUoZ9wEvwad3r4HXenA7j1B-hPae7BMc_c45WN9dPV3fF8vH2_upyWdiSibFwjtuGE2Fr1kphS-NIK2tHtRPOcF43AoxtLZWMmfxNCiaNllA50xItiGBzdLbNfY3D2wRpVL1PFrpOBximpFiuLHnDJM9SupXaOKQUwanX6HsdPxQl6huo2qgMVH0DVVug2XP6Ez-ZHto_xy_BLLjYCiCXfPcQVbIegoXWR7Cjagf_T_wXsweGag</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3146948394</pqid></control><display><type>article</type><title>Molecular characterization of the E2 conjugating enzyme LinfUbc13 in Leishmania infantum</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Rodrigues da Silva, Eduardo Vagner ; Torres, Caroline ; Nemamiah Escolarique Ribeiro, Hariel ; Santana Travaglini Berti de Correia, Camila Rolemberg ; de Oliveira de Castro, Taissa ; da Costa Mancin, Giovanna ; Zanchetta Venancio, Mayla Gabriela ; Abdel Baqui, Munira Muhammad ; Teixeira, Felipe Roberti ; Gomes, Marcelo Damário</creator><creatorcontrib>Rodrigues da Silva, Eduardo Vagner ; Torres, Caroline ; Nemamiah Escolarique Ribeiro, Hariel ; Santana Travaglini Berti de Correia, Camila Rolemberg ; de Oliveira de Castro, Taissa ; da Costa Mancin, Giovanna ; Zanchetta Venancio, Mayla Gabriela ; Abdel Baqui, Munira Muhammad ; Teixeira, Felipe Roberti ; Gomes, Marcelo Damário</creatorcontrib><description>UBC13 is an orthologue of Homo sapiens ubiquitin-conjugation E2 enzymes described in Leishmania mexicana, a null mutant lacking this gene cannot be produced, suggesting essential functions in this parasite. Leishmania infantum is an etiological agent of visceral leishmaniasis, the most severe type of disease that is potentially fatal if untreated. The ubiquitination process has been targeted for leishmanicidal compounds, indicating its essential function in parasite homeostasis. Therefore, the molecular characterization of the ubiquitination process may provide a better understanding of the molecular and cellular basis of leishmaniasis. Here, we characterized the gene LINF_350017900 in Leishmania infantum, which was named LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3. LinfUbc13 contains conserved catalytic residues, including Cys86 and the HPN motif, which are essential for ubiquitin-conjugating activity. Structural analysis revealed a high similarity between LinfUbc13 and human UBE2D proteins, with a root-mean-square deviation (RMSD) of 0.4 Å, suggesting conserved functions. Recombinant LinfUbc13 was expressed and shown to accept ubiquitin from E1, forming a thioester intermediate. Functional assays demonstrated that LinfUbc13 transfers ubiquitin to p53 through human HDM2 E3 ligase, confirming its role in ubiquitination. Subcellular localization showed that LinfUbc13 was distributed throughout the parasite cytoplasm. These findings highlight the conserved nature of the ubiquitin-proteasome system between Leishmania infantum and Homo sapiens, showing that LinfUbc13 is an E2 enzyme that plays a crucial role in parasitic development. [Display omitted] •LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3.•Recombinant LinfUbc13 is able to accept ubiquitin from E1, forming a thioester intermediate.•LinfUbc13 is present in the cytosol of parasites.•LinfUbc13 is an essential gene.</description><identifier>ISSN: 0003-9861</identifier><identifier>ISSN: 1096-0384</identifier><identifier>EISSN: 1096-0384</identifier><identifier>DOI: 10.1016/j.abb.2024.110272</identifier><identifier>PMID: 39689751</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino Acid Sequence ; E2-UB ; Humans ; Kinetoplastid ; Leishmania ; Leishmania infantum - enzymology ; Leishmania infantum - genetics ; Proteasome ; Proto-Oncogene Proteins c-mdm2 - chemistry ; Proto-Oncogene Proteins c-mdm2 - genetics ; Proto-Oncogene Proteins c-mdm2 - metabolism ; Protozoan Proteins - chemistry ; Protozoan Proteins - genetics ; Protozoan Proteins - metabolism ; Tumor Suppressor Protein p53 - chemistry ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism ; UBC13 ; Ubiquitin ; Ubiquitin-Conjugating Enzymes - chemistry ; Ubiquitin-Conjugating Enzymes - genetics ; Ubiquitin-Conjugating Enzymes - metabolism ; Ubiquitination</subject><ispartof>Archives of biochemistry and biophysics, 2025-02, Vol.764, p.110272, Article 110272</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c235t-ff4c8405c73d95c2bf0d97f1af5fb44785ebcdc1933bbc19539ba9e6fbd0a5053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0003986124003941$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39689751$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodrigues da Silva, Eduardo Vagner</creatorcontrib><creatorcontrib>Torres, Caroline</creatorcontrib><creatorcontrib>Nemamiah Escolarique Ribeiro, Hariel</creatorcontrib><creatorcontrib>Santana Travaglini Berti de Correia, Camila Rolemberg</creatorcontrib><creatorcontrib>de Oliveira de Castro, Taissa</creatorcontrib><creatorcontrib>da Costa Mancin, Giovanna</creatorcontrib><creatorcontrib>Zanchetta Venancio, Mayla Gabriela</creatorcontrib><creatorcontrib>Abdel Baqui, Munira Muhammad</creatorcontrib><creatorcontrib>Teixeira, Felipe Roberti</creatorcontrib><creatorcontrib>Gomes, Marcelo Damário</creatorcontrib><title>Molecular characterization of the E2 conjugating enzyme LinfUbc13 in Leishmania infantum</title><title>Archives of biochemistry and biophysics</title><addtitle>Arch Biochem Biophys</addtitle><description>UBC13 is an orthologue of Homo sapiens ubiquitin-conjugation E2 enzymes described in Leishmania mexicana, a null mutant lacking this gene cannot be produced, suggesting essential functions in this parasite. Leishmania infantum is an etiological agent of visceral leishmaniasis, the most severe type of disease that is potentially fatal if untreated. The ubiquitination process has been targeted for leishmanicidal compounds, indicating its essential function in parasite homeostasis. Therefore, the molecular characterization of the ubiquitination process may provide a better understanding of the molecular and cellular basis of leishmaniasis. Here, we characterized the gene LINF_350017900 in Leishmania infantum, which was named LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3. LinfUbc13 contains conserved catalytic residues, including Cys86 and the HPN motif, which are essential for ubiquitin-conjugating activity. Structural analysis revealed a high similarity between LinfUbc13 and human UBE2D proteins, with a root-mean-square deviation (RMSD) of 0.4 Å, suggesting conserved functions. Recombinant LinfUbc13 was expressed and shown to accept ubiquitin from E1, forming a thioester intermediate. Functional assays demonstrated that LinfUbc13 transfers ubiquitin to p53 through human HDM2 E3 ligase, confirming its role in ubiquitination. Subcellular localization showed that LinfUbc13 was distributed throughout the parasite cytoplasm. These findings highlight the conserved nature of the ubiquitin-proteasome system between Leishmania infantum and Homo sapiens, showing that LinfUbc13 is an E2 enzyme that plays a crucial role in parasitic development. [Display omitted] •LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3.•Recombinant LinfUbc13 is able to accept ubiquitin from E1, forming a thioester intermediate.•LinfUbc13 is present in the cytosol of parasites.•LinfUbc13 is an essential gene.</description><subject>Amino Acid Sequence</subject><subject>E2-UB</subject><subject>Humans</subject><subject>Kinetoplastid</subject><subject>Leishmania</subject><subject>Leishmania infantum - enzymology</subject><subject>Leishmania infantum - genetics</subject><subject>Proteasome</subject><subject>Proto-Oncogene Proteins c-mdm2 - chemistry</subject><subject>Proto-Oncogene Proteins c-mdm2 - genetics</subject><subject>Proto-Oncogene Proteins c-mdm2 - metabolism</subject><subject>Protozoan Proteins - chemistry</subject><subject>Protozoan Proteins - genetics</subject><subject>Protozoan Proteins - metabolism</subject><subject>Tumor Suppressor Protein p53 - chemistry</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><subject>UBC13</subject><subject>Ubiquitin</subject><subject>Ubiquitin-Conjugating Enzymes - chemistry</subject><subject>Ubiquitin-Conjugating Enzymes - genetics</subject><subject>Ubiquitin-Conjugating Enzymes - metabolism</subject><subject>Ubiquitination</subject><issn>0003-9861</issn><issn>1096-0384</issn><issn>1096-0384</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9LxDAQxYMouq5-AC-So5euSZO0DZ5E_AcrXlzwFpJ04mZpU01aQT-9kVWPnoYZ3nvD-yF0QsmCElqdbxbamEVJSr6glJR1uYNmlMiqIKzhu2hGCGGFbCp6gA5T2hBCKa_KfXTAZNXIWtAZen4YOrBTpyO2ax21HSH6Tz36IeDB4XEN-LrEdgib6SVfwwuG8PnRA1764FbGUoZ9wEvwad3r4HXenA7j1B-hPae7BMc_c45WN9dPV3fF8vH2_upyWdiSibFwjtuGE2Fr1kphS-NIK2tHtRPOcF43AoxtLZWMmfxNCiaNllA50xItiGBzdLbNfY3D2wRpVL1PFrpOBximpFiuLHnDJM9SupXaOKQUwanX6HsdPxQl6huo2qgMVH0DVVug2XP6Ez-ZHto_xy_BLLjYCiCXfPcQVbIegoXWR7Cjagf_T_wXsweGag</recordid><startdate>202502</startdate><enddate>202502</enddate><creator>Rodrigues da Silva, Eduardo Vagner</creator><creator>Torres, Caroline</creator><creator>Nemamiah Escolarique Ribeiro, Hariel</creator><creator>Santana Travaglini Berti de Correia, Camila Rolemberg</creator><creator>de Oliveira de Castro, Taissa</creator><creator>da Costa Mancin, Giovanna</creator><creator>Zanchetta Venancio, Mayla Gabriela</creator><creator>Abdel Baqui, Munira Muhammad</creator><creator>Teixeira, Felipe Roberti</creator><creator>Gomes, Marcelo Damário</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>202502</creationdate><title>Molecular characterization of the E2 conjugating enzyme LinfUbc13 in Leishmania infantum</title><author>Rodrigues da Silva, Eduardo Vagner ; Torres, Caroline ; Nemamiah Escolarique Ribeiro, Hariel ; Santana Travaglini Berti de Correia, Camila Rolemberg ; de Oliveira de Castro, Taissa ; da Costa Mancin, Giovanna ; Zanchetta Venancio, Mayla Gabriela ; Abdel Baqui, Munira Muhammad ; Teixeira, Felipe Roberti ; Gomes, Marcelo Damário</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c235t-ff4c8405c73d95c2bf0d97f1af5fb44785ebcdc1933bbc19539ba9e6fbd0a5053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Amino Acid Sequence</topic><topic>E2-UB</topic><topic>Humans</topic><topic>Kinetoplastid</topic><topic>Leishmania</topic><topic>Leishmania infantum - enzymology</topic><topic>Leishmania infantum - genetics</topic><topic>Proteasome</topic><topic>Proto-Oncogene Proteins c-mdm2 - chemistry</topic><topic>Proto-Oncogene Proteins c-mdm2 - genetics</topic><topic>Proto-Oncogene Proteins c-mdm2 - metabolism</topic><topic>Protozoan Proteins - chemistry</topic><topic>Protozoan Proteins - genetics</topic><topic>Protozoan Proteins - metabolism</topic><topic>Tumor Suppressor Protein p53 - chemistry</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><topic>UBC13</topic><topic>Ubiquitin</topic><topic>Ubiquitin-Conjugating Enzymes - chemistry</topic><topic>Ubiquitin-Conjugating Enzymes - genetics</topic><topic>Ubiquitin-Conjugating Enzymes - metabolism</topic><topic>Ubiquitination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodrigues da Silva, Eduardo Vagner</creatorcontrib><creatorcontrib>Torres, Caroline</creatorcontrib><creatorcontrib>Nemamiah Escolarique Ribeiro, Hariel</creatorcontrib><creatorcontrib>Santana Travaglini Berti de Correia, Camila Rolemberg</creatorcontrib><creatorcontrib>de Oliveira de Castro, Taissa</creatorcontrib><creatorcontrib>da Costa Mancin, Giovanna</creatorcontrib><creatorcontrib>Zanchetta Venancio, Mayla Gabriela</creatorcontrib><creatorcontrib>Abdel Baqui, Munira Muhammad</creatorcontrib><creatorcontrib>Teixeira, Felipe Roberti</creatorcontrib><creatorcontrib>Gomes, Marcelo Damário</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of biochemistry and biophysics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodrigues da Silva, Eduardo Vagner</au><au>Torres, Caroline</au><au>Nemamiah Escolarique Ribeiro, Hariel</au><au>Santana Travaglini Berti de Correia, Camila Rolemberg</au><au>de Oliveira de Castro, Taissa</au><au>da Costa Mancin, Giovanna</au><au>Zanchetta Venancio, Mayla Gabriela</au><au>Abdel Baqui, Munira Muhammad</au><au>Teixeira, Felipe Roberti</au><au>Gomes, Marcelo Damário</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular characterization of the E2 conjugating enzyme LinfUbc13 in Leishmania infantum</atitle><jtitle>Archives of biochemistry and biophysics</jtitle><addtitle>Arch Biochem Biophys</addtitle><date>2025-02</date><risdate>2025</risdate><volume>764</volume><spage>110272</spage><pages>110272-</pages><artnum>110272</artnum><issn>0003-9861</issn><issn>1096-0384</issn><eissn>1096-0384</eissn><abstract>UBC13 is an orthologue of Homo sapiens ubiquitin-conjugation E2 enzymes described in Leishmania mexicana, a null mutant lacking this gene cannot be produced, suggesting essential functions in this parasite. Leishmania infantum is an etiological agent of visceral leishmaniasis, the most severe type of disease that is potentially fatal if untreated. The ubiquitination process has been targeted for leishmanicidal compounds, indicating its essential function in parasite homeostasis. Therefore, the molecular characterization of the ubiquitination process may provide a better understanding of the molecular and cellular basis of leishmaniasis. Here, we characterized the gene LINF_350017900 in Leishmania infantum, which was named LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3. LinfUbc13 contains conserved catalytic residues, including Cys86 and the HPN motif, which are essential for ubiquitin-conjugating activity. Structural analysis revealed a high similarity between LinfUbc13 and human UBE2D proteins, with a root-mean-square deviation (RMSD) of 0.4 Å, suggesting conserved functions. Recombinant LinfUbc13 was expressed and shown to accept ubiquitin from E1, forming a thioester intermediate. Functional assays demonstrated that LinfUbc13 transfers ubiquitin to p53 through human HDM2 E3 ligase, confirming its role in ubiquitination. Subcellular localization showed that LinfUbc13 was distributed throughout the parasite cytoplasm. These findings highlight the conserved nature of the ubiquitin-proteasome system between Leishmania infantum and Homo sapiens, showing that LinfUbc13 is an E2 enzyme that plays a crucial role in parasitic development. [Display omitted] •LinfUBC13, an E2 orthologue of UBC13 in Leishmania mexicana and the UBE2D family in Homo sapiens, sharing 72–74 % identity with UBE2D1, UBE2D2, and UBE2D3.•Recombinant LinfUbc13 is able to accept ubiquitin from E1, forming a thioester intermediate.•LinfUbc13 is present in the cytosol of parasites.•LinfUbc13 is an essential gene.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39689751</pmid><doi>10.1016/j.abb.2024.110272</doi></addata></record>
fulltext fulltext
identifier ISSN: 0003-9861
ispartof Archives of biochemistry and biophysics, 2025-02, Vol.764, p.110272, Article 110272
issn 0003-9861
1096-0384
1096-0384
language eng
recordid cdi_proquest_miscellaneous_3146948394
source MEDLINE; Elsevier ScienceDirect Journals
subjects Amino Acid Sequence
E2-UB
Humans
Kinetoplastid
Leishmania
Leishmania infantum - enzymology
Leishmania infantum - genetics
Proteasome
Proto-Oncogene Proteins c-mdm2 - chemistry
Proto-Oncogene Proteins c-mdm2 - genetics
Proto-Oncogene Proteins c-mdm2 - metabolism
Protozoan Proteins - chemistry
Protozoan Proteins - genetics
Protozoan Proteins - metabolism
Tumor Suppressor Protein p53 - chemistry
Tumor Suppressor Protein p53 - genetics
Tumor Suppressor Protein p53 - metabolism
UBC13
Ubiquitin
Ubiquitin-Conjugating Enzymes - chemistry
Ubiquitin-Conjugating Enzymes - genetics
Ubiquitin-Conjugating Enzymes - metabolism
Ubiquitination
title Molecular characterization of the E2 conjugating enzyme LinfUbc13 in Leishmania infantum
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T14%3A57%3A30IST&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=Molecular%20characterization%20of%20the%20E2%20conjugating%20enzyme%20LinfUbc13%20in%20Leishmania%20infantum&rft.jtitle=Archives%20of%20biochemistry%20and%20biophysics&rft.au=Rodrigues%20da%20Silva,%20Eduardo%20Vagner&rft.date=2025-02&rft.volume=764&rft.spage=110272&rft.pages=110272-&rft.artnum=110272&rft.issn=0003-9861&rft.eissn=1096-0384&rft_id=info:doi/10.1016/j.abb.2024.110272&rft_dat=%3Cproquest_cross%3E3146948394%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=3146948394&rft_id=info:pmid/39689751&rft_els_id=S0003986124003941&rfr_iscdi=true