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Difference between revisions of "User:Plinio Vieira"

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Plinio Vieira obtained his B.Sc. Lic. in Chemistry from the University of São Paulo (2010) and his Ph.D. (2016) at the University of Campinas under the supervision of [[User:Mario Murakami|Mario Murakami]]. The work focused on the crystallographic studies of NEK kinases from Trypanosomatids, aiming for structural-based drug design. During his post-doc at [https://cnpem.br/ Brazilian National Center for Research in Energy and Materials] under the supervision of Dr. Murakami, he studied Glycoside Hydrolases from ''Xanthomonas'' that act on Xyloglucan depolymerization. He also developed a post-doc project under the supervision of [https://miguelalcaldelab.eu/contact/ Miguel Alcalde] at [https://icp.csic.es/ Institute of Catalysis and Petrochemistry], focusing on the random and semi-rational evolution of a GH35 β-galactosidase. He currently works as Researcher Specialist at [https://lnbr.cnpem.br Brazilian Biorenewables Laboratory], focusing on the discovery and the structure-function-mechanism relationship from CAZymes. He has contributed for the tridimensional structure determination of:
 
Plinio Vieira obtained his B.Sc. Lic. in Chemistry from the University of São Paulo (2010) and his Ph.D. (2016) at the University of Campinas under the supervision of [[User:Mario Murakami|Mario Murakami]]. The work focused on the crystallographic studies of NEK kinases from Trypanosomatids, aiming for structural-based drug design. During his post-doc at [https://cnpem.br/ Brazilian National Center for Research in Energy and Materials] under the supervision of Dr. Murakami, he studied Glycoside Hydrolases from ''Xanthomonas'' that act on Xyloglucan depolymerization. He also developed a post-doc project under the supervision of [https://miguelalcaldelab.eu/contact/ Miguel Alcalde] at [https://icp.csic.es/ Institute of Catalysis and Petrochemistry], focusing on the random and semi-rational evolution of a GH35 β-galactosidase. He currently works as Researcher Specialist at [https://lnbr.cnpem.br Brazilian Biorenewables Laboratory], focusing on the discovery and the structure-function-mechanism relationship from CAZymes. He has contributed for the tridimensional structure determination of:
*[[CE20]] '''Family first''' ''Xanthomonas citri'' pv. ''citri'' xyloglucan acetylesterase [https://www.rcsb.org/structure/7KMM PDB ID 7KMM]
 
  
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-β-mannanase [https://www.rcsb.org/structure/6BYC PDB ID 6BYC]
+
*[[CE20]] '''Family first''' ''Xanthomonas citri'' pv. ''citri'' xyloglucan acetylesterase [https://www.rcsb.org/structure/7KMM PDB ID 7KMM] <ref>Vieira2021</ref>
 
+
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-mannanase [https://www.rcsb.org/structure/6BYC PDB ID 6BYC] <ref>Domingues2018</ref>
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-mannanase, in complex with mannose [https://www.rcsb.org/structure/6BYE PDB ID 6BYE]
+
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-mannanase, in complex with mannose [https://www.rcsb.org/structure/6BYE PDB ID 6BYE] <ref>Domingues2018</ref>
 
+
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-mannanase mutant E477A [https://www.rcsb.org/structure/6BYI PDB ID 6BYI] <ref>Domingues2018</ref>
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-mannanase mutant E477A [https://www.rcsb.org/structure/6BYI PDB ID 6BYI]
+
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-mannanase mutant E575A [https://www.rcsb.org/structure/6BYG PDB ID 6BYG] <ref>Domingues2018</ref>
 
+
*[[GH31]] ''Xanthomonas citri'' pv. ''citri'' exo-&alpha;-xylosidase [https://www.rcsb.org/structure/7KMP PDB ID 7KMP] <ref>Vieira2021</ref>
*[[GH2]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-mannanase mutant E575A [https://www.rcsb.org/structure/6BYG PDB ID 6BYG]
+
*[[GH31]] ''Xanthomonas citri'' pv. ''citri'' exo-&alpha;-xylosidase, in complex with xylose [https://www.rcsb.org/structure/7KNC PDB ID 7KNC] <ref>Vieira2021</ref>
 
+
*[[GH35]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-galactosidase [https://www.rcsb.org/structure/7KMN PDB ID 7KMN] <ref>Vieira2021</ref>
*[[GH31]] ''Xanthomonas citri'' pv. ''citri'' exo-&alpha;-xylosidase [https://www.rcsb.org/structure/7KMP PDB ID 7KMP]
+
*[[GH35]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-galactosidase, in complex with galactose [https://www.rcsb.org/structure/7KMO PDB ID 7KMO] <ref>Vieira2021</ref>
 
+
*[[GH74]] ''Xanthomonas campestris'' pv. ''campestris'' endo-xyloglucanase, in complex with XG oligosaccharide [https://www.rcsb.org/structure/7KN8 PDB ID 7KN8] <ref>Vieira2021</ref>
*[[GH31]] ''Xanthomonas citri'' pv. ''citri'' exo-&alpha;-xylosidase, in complex with xylose [https://www.rcsb.org/structure/7KNC PDB ID 7KNC]
+
*[[GH95]] ''Xanthomonas citri'' pv. ''citri'' &alpha;-L-1,2-fucosidase [https://www.rcsb.org/structure/7KMQ PDB ID 7KMQ] <ref>Vieira2021</ref>
 
+
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E102A mutant, in complex with laminaritriose and laminaribiose [https://www.rcsb.org/structure/6UAU PDB ID 6UAU] <ref>Santos2020</ref>
*[[GH35]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-galactosidase [https://www.rcsb.org/structure/7KMN PDB ID 7KMN]
+
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E102A mutant, in complex with laminaripentaose [https://www.rcsb.org/structure/6UAT PDB ID 6UAT] <ref>Santos2020</ref>
 
+
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E199Q mutant [https://www.rcsb.org/structure/6UFZ PDB ID 6UBFZ] <ref>Santos2020</ref>
*[[GH35]] ''Xanthomonas citri'' pv. ''citri'' exo-&beta;-galactosidase, in complex with galactose [https://www.rcsb.org/structure/7KMO PDB ID 7KMO]
+
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E199A mutant, in complex with laminaripentaose [https://www.rcsb.org/structure/6UAS/ PDB ID 6UAS] <ref>Santos2020</ref>
 
+
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E199A mutant, in complex with laminarihexaose [https://www.rcsb.org/structure/6UFL PDB ID 6UFL] <ref>Santos2020</ref>
*[[GH74]] ''Xanthomonas campestris'' pv. ''campestris'' endo-xyloglucanase, in complex with XG oligosaccharide [https://www.rcsb.org/structure/7KN8 PDB ID 7KN8]
+
*[[GH128]] ''Sorangium cellulosum'' endo-&beta;-1,3-glucanase [https://www.rcsb.org/structure/6UAX/ PDB ID 6UAX] <ref>Santos2020</ref>
 
+
*[[GH128]] ''Lentinula edodes'' endo-&beta;-1,3-glucanase [https://www.rcsb.org/structure/6UB2 PDB ID 6UB2] <ref>Santos2020</ref>
*[[GH35]] ''Xanthomonas citri'' pv. ''citri'' &alpha;-L-1,2-fucosidase [https://www.rcsb.org/structure/7KMQ PDB ID 7KMQ]
+
*[[GH128]] ''Aureobasidium namibiae'' exo-&beta;-1,3-glucanase [https://www.rcsb.org/structure/6UB8 PDB ID 6UB8] <ref>Santos2020</ref>
 
+
*[[GH128]] ''Aureobasidium namibiae'' exo-&beta;-1,3-glucanase, in complex with laminaritriose [https://www.rcsb.org/structure/6UBA PDB ID 6UAB] <ref>Santos2020</ref>
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E102A mutant, in complex with laminaritriose and laminaribiose [https://www.rcsb.org/structure/6UAU PDB ID 6UAU]
+
*[[GH128]] ''Aureobasidium namibiae'' exo-&beta;-1,3-glucanase, with laminaribiose at the surface-binding site [https://www.rcsb.org/structure/6UBB PDB ID 6UBB] <ref>Santos2020</ref>
 
+
*[[GH128]] ''Cryptococcus neoformans'' oligosaccharide-binding protein [https://www.rcsb.org/structure/6UBC PDB ID 6UBC] <ref>Santos2020</ref>
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E102A mutant, in complex with laminaripentaose [https://www.rcsb.org/structure/6UAT PDB ID 6UAT]
 
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E199Q mutant [https://www.rcsb.org/structure/6UFZ PDB ID 6UBFZ]
 
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E199A mutant, in complex with laminaripentaose [https://www.rcsb.org/structure/6UAS/ PDB ID 6UAS]
 
*[[GH128]] ''Amycolatopsis mediterranei'' endo-&beta;-1,3-glucanase E199A mutant, in complex with laminarihexaose [https://www.rcsb.org/structure/6UFL PDB ID 6UFL]
 
*[[GH128]] ''Sorangium cellulosum'' endo-&beta;-1,3-glucanase [https://www.rcsb.org/structure/6UAX/ PDB ID 6UAX]
 
*[[GH128]] ''Lentinula edodes'' endo-&beta;-1,3-glucanase [https://www.rcsb.org/structure/6UB2 PDB ID 6UB2]
 
*[[GH128]] ''Aureobasidium namibiae'' exo-&beta;-1,3-glucanase [https://www.rcsb.org/structure/6UB8 PDB ID 6UB8]
 
*[[GH128]] ''Aureobasidium namibiae'' exo-&beta;-1,3-glucanase, in complex with laminaritriose [https://www.rcsb.org/structure/6UBA PDB ID 6UAB]
 
*[[GH128]] ''Aureobasidium namibiae'' exo-&beta;-1,3-glucanase, with laminaribiose at the surface-binding site [https://www.rcsb.org/structure/6UBB PDB ID 6UBB]
 
*[[GH128]] ''Cryptococcus neoformans'' oligosaccharide-binding protein [https://www.rcsb.org/structure/6UBC PDB ID 6UBC]
 
  
  
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<biblio>
 
<biblio>
  
# Gilbert2008 pmid=18430603
+
#Vieira2021 pmid=34193873
 +
 
 +
#Santos2020 pmid=32451508
  
 +
#Domingues2018 pmid=29997257
 
</biblio>
 
</biblio>
  

Revision as of 12:04, 24 January 2023

Blank user-200px.png

Plinio Vieira obtained his B.Sc. Lic. in Chemistry from the University of São Paulo (2010) and his Ph.D. (2016) at the University of Campinas under the supervision of Mario Murakami. The work focused on the crystallographic studies of NEK kinases from Trypanosomatids, aiming for structural-based drug design. During his post-doc at Brazilian National Center for Research in Energy and Materials under the supervision of Dr. Murakami, he studied Glycoside Hydrolases from Xanthomonas that act on Xyloglucan depolymerization. He also developed a post-doc project under the supervision of Miguel Alcalde at Institute of Catalysis and Petrochemistry, focusing on the random and semi-rational evolution of a GH35 β-galactosidase. He currently works as Researcher Specialist at Brazilian Biorenewables Laboratory, focusing on the discovery and the structure-function-mechanism relationship from CAZymes. He has contributed for the tridimensional structure determination of:



  1. Vieira PS, Bonfim IM, Araujo EA, Melo RR, Lima AR, Fessel MR, Paixão DAA, Persinoti GF, Rocco SA, Lima TB, Pirolla RAS, Morais MAB, Correa JBL, Zanphorlin LM, Diogo JA, Lima EA, Grandis A, Buckeridge MS, Gozzo FC, Benedetti CE, Polikarpov I, Giuseppe PO, and Murakami MT. (2021). Xyloglucan processing machinery in Xanthomonas pathogens and its role in the transcriptional activation of virulence factors. Nat Commun. 2021;12(1):4049. DOI:10.1038/s41467-021-24277-4 | PubMed ID:34193873 [Vieira2021]
  2. Santos CR, Costa PACR, Vieira PS, Gonzalez SET, Correa TLR, Lima EA, Mandelli F, Pirolla RAS, Domingues MN, Cabral L, Martins MP, Cordeiro RL, Junior AT, Souza BP, Prates ÉT, Gozzo FC, Persinoti GF, Skaf MS, and Murakami MT. (2020). Structural insights into β-1,3-glucan cleavage by a glycoside hydrolase family. Nat Chem Biol. 2020;16(8):920-929. DOI:10.1038/s41589-020-0554-5 | PubMed ID:32451508 [Santos2020]
  3. Domingues MN, Souza FHM, Vieira PS, de Morais MAB, Zanphorlin LM, Dos Santos CR, Pirolla RAS, Honorato RV, de Oliveira PSL, Gozzo FC, and Murakami MT. (2018). Structural basis of exo-β-mannanase activity in the GH2 family. J Biol Chem. 2018;293(35):13636-13649. DOI:10.1074/jbc.RA118.002374 | PubMed ID:29997257 [Domingues2018]

All Medline abstracts: PubMed

  1. Vieira2021
  2. Domingues2018
  3. Domingues2018
  4. Domingues2018
  5. Domingues2018
  6. Vieira2021
  7. Vieira2021
  8. Vieira2021
  9. Vieira2021
  10. Vieira2021
  11. Vieira2021
  12. Santos2020
  13. Santos2020
  14. Santos2020
  15. Santos2020
  16. Santos2020
  17. Santos2020
  18. Santos2020
  19. Santos2020
  20. Santos2020
  21. Santos2020
  22. Santos2020