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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''' [https://www.rcsb.org/structure/7KMM ''Xac''XaeA] <cite>Vieira2021</cite> |
*[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYC PDB ID 6BYC] <cite>Domingues2018</cite> | *[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYC PDB ID 6BYC] <cite>Domingues2018</cite> | ||
*[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYE PDB ID 6BYE] <cite>Domingues2018</cite> | *[[GH2]] ''Xac''Man2A [https://www.rcsb.org/structure/6BYE PDB ID 6BYE] <cite>Domingues2018</cite> | ||
Revision as of 07:34, 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 [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]
Error fetching PMID 32451508:
Error fetching PMID 29997257:
- Error fetching PMID 34193873:
- Error fetching PMID 29997257:
- Error fetching PMID 32451508: