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Difference between revisions of "User:Plinio Vieira"
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Plinio Salmazo 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]] and [[User:Priscila Giuseppe|Priscila Oliveira de Giuseppe]]. 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 worked on 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 Salmazo 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]] and [[User:Priscila Giuseppe|Priscila Oliveira de Giuseppe]]. 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 worked on 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'' | + | *[[CE20]] '''Family first''' 'Xac''XaeA [https://www.rcsb.org/structure/7KMM PDB ID 7KMM] <cite>Vieira2021</cite> |
| − | *[[GH2]] | + | *[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYC PDB ID 6BYC] <cite>Domingues2018</cite> |
| − | *[[GH2]] | + | *[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYE PDB ID 6BYE] <cite>Domingues2018</cite> |
| − | *[[GH2]] | + | *[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYI PDB ID 6BYI] <cite>Domingues2018</cite> |
| − | *[[GH2]] | + | *[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYG PDB ID 6BYG] <cite>Domingues2018</cite> |
| − | *[[GH31]] | + | *[[GH31]] ''Xac''Xyl31 [https://www.rcsb.org/structure/7KMP PDB ID 7KMP] <cite>Vieira2021</cite> |
| − | *[[GH31]] | + | *[[GH31]] ''Xac''Xyl31 [https://www.rcsb.org/structure/7KNC PDB ID 7KNC] <cite>Vieira2021</cite> |
| − | *[[GH35]] | + | *[[GH35]] ''Xac''GalD [https://www.rcsb.org/structure/7KMN PDB ID 7KMN] <cite>Vieira2021</cite> |
| − | *[[GH35]] | + | *[[GH35]] ''Xac''GalD [https://www.rcsb.org/structure/7KMO PDB ID 7KMO] <cite>Vieira2021</cite> |
| − | *[[GH74]] | + | *[[GH74]] ''Xcc''Xeg74 [https://www.rcsb.org/structure/7KN8 PDB ID 7KN8] <cite>Vieira2021</cite> |
| − | *[[GH95]] | + | *[[GH95]] ''Xac''Afc95 [https://www.rcsb.org/structure/7KMQ PDB ID 7KMQ] <cite>Vieira2021</cite> |
| − | *[[GH128]] | + | *[[GH128]] AmGH128_I [https://www.rcsb.org/structure/6UAU PDB ID 6UAU] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] AmGH128_I [https://www.rcsb.org/structure/6UAT PDB ID 6UAT] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] AmGH128_I [https://www.rcsb.org/structure/6UFZ PDB ID 6UBFZ] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] AmGH128_I [https://www.rcsb.org/structure/6UAS/ PDB ID 6UAS] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] AmGH128_I [https://www.rcsb.org/structure/6UFL PDB ID 6UFL] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] ScGH128_II [https://www.rcsb.org/structure/6UAX/ PDB ID 6UAX] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] LeGH128_IV [https://www.rcsb.org/structure/6UB2 PDB ID 6UB2] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] AnGH128_VI [https://www.rcsb.org/structure/6UB8 PDB ID 6UB8] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] AnGH128_VI [https://www.rcsb.org/structure/6UBA PDB ID 6UAB] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] AnGH128_VI [https://www.rcsb.org/structure/6UBB PDB ID 6UBB] <cite>Santos2020</cite> |
| − | *[[GH128]] | + | *[[GH128]] CnGH128_VII [https://www.rcsb.org/structure/6UBC PDB ID 6UBC] <cite>Santos2020</cite> |
---- | ---- | ||
Revision as of 08:33, 22 March 2023
Plinio Salmazo 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 and Priscila Oliveira de Giuseppe. 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 worked on 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:
- CE20 Family first 'XacXaeA PDB ID 7KMM [1]
- GH2 XacMan2A PDB ID 6BYC [2]
- GH2 XacMan2A PDB ID 6BYE [2]
- GH2 XacMan2A PDB ID 6BYI [2]
- GH2 XacMan2A PDB ID 6BYG [2]
- GH31 XacXyl31 PDB ID 7KMP [1]
- GH31 XacXyl31 PDB ID 7KNC [1]
- GH35 XacGalD PDB ID 7KMN [1]
- GH35 XacGalD PDB ID 7KMO [1]
- GH74 XccXeg74 PDB ID 7KN8 [1]
- GH95 XacAfc95 PDB ID 7KMQ [1]
- GH128 AmGH128_I PDB ID 6UAU [3]
- GH128 AmGH128_I PDB ID 6UAT [3]
- GH128 AmGH128_I PDB ID 6UBFZ [3]
- GH128 AmGH128_I PDB ID 6UAS [3]
- GH128 AmGH128_I PDB ID 6UFL [3]
- GH128 ScGH128_II PDB ID 6UAX [3]
- GH128 LeGH128_IV PDB ID 6UB2 [3]
- GH128 AnGH128_VI PDB ID 6UB8 [3]
- GH128 AnGH128_VI PDB ID 6UAB [3]
- GH128 AnGH128_VI PDB ID 6UBB [3]
- GH128 CnGH128_VII PDB ID 6UBC [3]
- 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 |
- 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 |
- 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 |