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Artigo de periodico
In silico screening strategies for novel inhibitors of parasitic diseases (2011)
Ferreira, Rafaela S.; Guido, Rafael Victorio Carvalho ; Andricopulo, Adriano Defini ; Oliva, Glaucius
Source: Expert Opinion on Drug Discovery. Unidade: IFSC
Subjects: DOENÇAS PARASITÁRIAS (ESTUDO;TRATAMENTO), PLANEJAMENTO DE FÁRMACOS, INIBIDORES DE ENZIMAS, TRYPANOSOMA CRUZI
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ABNT
FERREIRA, Rafaela S. et al. In silico screening strategies for novel inhibitors of parasitic diseases. Expert Opinion on Drug Discovery, v. 6, n. 5, p. 481-489, 2011Tradução . . Disponível em: https://doi.org/10.1517/17460441.2011.563297. Acesso em: 15 nov. 2024.
APA
Ferreira, R. S., Guido, R. V. C., Andricopulo, A. D., & Oliva, G. (2011). In silico screening strategies for novel inhibitors of parasitic diseases. Expert Opinion on Drug Discovery, 6( 5), 481-489. doi:10.1517/17460441.2011.563297
NLM
Ferreira RS, Guido RVC, Andricopulo AD, Oliva G. In silico screening strategies for novel inhibitors of parasitic diseases [Internet]. Expert Opinion on Drug Discovery. 2011 ; 6( 5): 481-489.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1517/17460441.2011.563297
Vancouver
Ferreira RS, Guido RVC, Andricopulo AD, Oliva G. In silico screening strategies for novel inhibitors of parasitic diseases [Internet]. Expert Opinion on Drug Discovery. 2011 ; 6( 5): 481-489.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1517/17460441.2011.563297
Artigo de periodico
Adenosine binding to low-molecular-weight purine nucleoside phosphorylase: the structural basis for recognition based on its complex with the enzyme from Schistosoma mansoni (2010)
Pereira, Humberto d'Muniz; Rezende, Martha M.; Castilho, Marcelo Santos; Oliva, Glaucius ; Garratt, Richard Charles
Source: Acta Crystallographica D. Unidade: IFSC
Subjects: SCHISTOSOMA MANSONI, ENZIMAS, NUCLEOSÍDEOS
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ABNT
PEREIRA, Humberto d'Muniz et al. Adenosine binding to low-molecular-weight purine nucleoside phosphorylase: the structural basis for recognition based on its complex with the enzyme from Schistosoma mansoni. Acta Crystallographica D, v. 66, n. Ja 2010, p. 73-79, 2010Tradução . . Disponível em: https://doi.org/10.1107/S0907444909045715. Acesso em: 15 nov. 2024.
APA
Pereira, H. d'M., Rezende, M. M., Castilho, M. S., Oliva, G., & Garratt, R. C. (2010). Adenosine binding to low-molecular-weight purine nucleoside phosphorylase: the structural basis for recognition based on its complex with the enzyme from Schistosoma mansoni. Acta Crystallographica D, 66( Ja 2010), 73-79. doi:10.1107/S0907444909045715
NLM
Pereira H d'M, Rezende MM, Castilho MS, Oliva G, Garratt RC. Adenosine binding to low-molecular-weight purine nucleoside phosphorylase: the structural basis for recognition based on its complex with the enzyme from Schistosoma mansoni [Internet]. Acta Crystallographica D. 2010 ; 66( Ja 2010): 73-79.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1107/S0907444909045715
Vancouver
Pereira H d'M, Rezende MM, Castilho MS, Oliva G, Garratt RC. Adenosine binding to low-molecular-weight purine nucleoside phosphorylase: the structural basis for recognition based on its complex with the enzyme from Schistosoma mansoni [Internet]. Acta Crystallographica D. 2010 ; 66( Ja 2010): 73-79.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1107/S0907444909045715
Artigo de periodico
Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies (2010)
Castilho, Marcelo S.; Postigo, Matheus P.; Pereira, Humberto d'Muniz; Oliva, Glaucius ; Andricopulo, Adriano Defini
Source: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, INIBIDORES DE ENZIMAS, SCHISTOSOMA MANSONI
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ABNT
CASTILHO, Marcelo S. et al. Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies. Bioorganic and Medicinal Chemistry, v. 18, n. 4, p. 1421-1427, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2010.01.022. Acesso em: 15 nov. 2024.
APA
Castilho, M. S., Postigo, M. P., Pereira, H. d'M., Oliva, G., & Andricopulo, A. D. (2010). Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies. Bioorganic and Medicinal Chemistry, 18( 4), 1421-1427. doi:10.1016/j.bmc.2010.01.022
NLM
Castilho MS, Postigo MP, Pereira H d'M, Oliva G, Andricopulo AD. Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 4): 1421-1427.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2010.01.022
Vancouver
Castilho MS, Postigo MP, Pereira H d'M, Oliva G, Andricopulo AD. Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 4): 1421-1427.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2010.01.022
Artigo de periodico
Discovery of novel Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase inhibitors (2009)
Freitas, Renato F.; Prokopczyk, Igor M.; Zottis, Aderson; Oliva, Glaucius ; Andricopulo, Adriano Defini ; Trevisan, Maria Teresa S.; Vilegas, Wagner; Silva, Maria Goretti V.; Montanari, Carlos Alberto
Source: Bioorganic and Medicinal Chemistry. Unidades: IFSC, IQSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, FÁRMACOS (DESENVOLVIMENTO), INIBIDORES DE ENZIMAS, FARMACODINÂMICA
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ABNT
FREITAS, Renato F. et al. Discovery of novel Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase inhibitors. Bioorganic and Medicinal Chemistry, v. 17, n. 6, p. 2476-2482, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2009.01.079. Acesso em: 15 nov. 2024.
APA
Freitas, R. F., Prokopczyk, I. M., Zottis, A., Oliva, G., Andricopulo, A. D., Trevisan, M. T. S., et al. (2009). Discovery of novel Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase inhibitors. Bioorganic and Medicinal Chemistry, 17( 6), 2476-2482. doi:10.1016/j.bmc.2009.01.079
NLM
Freitas RF, Prokopczyk IM, Zottis A, Oliva G, Andricopulo AD, Trevisan MTS, Vilegas W, Silva MGV, Montanari CA. Discovery of novel Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 6): 2476-2482.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2009.01.079
Vancouver
Freitas RF, Prokopczyk IM, Zottis A, Oliva G, Andricopulo AD, Trevisan MTS, Vilegas W, Silva MGV, Montanari CA. Discovery of novel Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 6): 2476-2482.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2009.01.079
Editor de periodico
Acta Crystallographica D (2008)
Kostorz, G. (Editor); Oliva, Glaucius (Editor)
Unidade: IFSC
Subjects: CRISTALOGRAFIA, BIOLOGIA (ESTRUTURA), PROTEÍNAS
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ABNT
Acta Crystallographica D. . Chester: International Union of Crystallography - IUCr. . Acesso em: 15 nov. 2024. , 2008
APA
Acta Crystallographica D. (2008). Acta Crystallographica D. Chester: International Union of Crystallography - IUCr.
NLM
Acta Crystallographica D. 2008 ;[citado 2024 nov. 15 ]
Vancouver
Acta Crystallographica D. 2008 ;[citado 2024 nov. 15 ]
Artigo de periodico
The development of an immobilized enzyme reactor containing glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzy: the effect of species' specific differences on the immobilization (2008)
Cardoso, Carmen Lúcia; Moraes, Marcela Cristina de; Guido, Rafael Victorio Carvalho ; Oliva, Glaucius ; Andricopulo, Adriano Defini ; Wainer, Irving William; Cass, Quezia Bezerra
Source: Analyst. Unidades: FFCLRP, IFSC
Subjects: TRYPANOSOMA CRUZI, FÁRMACOS (DESENVOLVIMENTO), DOENÇA DE CHAGAS, ENZIMAS
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ABNT
CARDOSO, Carmen Lúcia et al. The development of an immobilized enzyme reactor containing glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzy: the effect of species' specific differences on the immobilization. Analyst, v. 133, n. Ja 2008, p. 93-99, 2008Tradução . . Disponível em: https://doi.org/10.1039/b711145b. Acesso em: 15 nov. 2024.
APA
Cardoso, C. L., Moraes, M. C. de, Guido, R. V. C., Oliva, G., Andricopulo, A. D., Wainer, I. W., & Cass, Q. B. (2008). The development of an immobilized enzyme reactor containing glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzy: the effect of species' specific differences on the immobilization. Analyst, 133( Ja 2008), 93-99. doi:10.1039/b711145b
NLM
Cardoso CL, Moraes MC de, Guido RVC, Oliva G, Andricopulo AD, Wainer IW, Cass QB. The development of an immobilized enzyme reactor containing glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzy: the effect of species' specific differences on the immobilization [Internet]. Analyst. 2008 ; 133( Ja 2008): 93-99.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1039/b711145b
Vancouver
Cardoso CL, Moraes MC de, Guido RVC, Oliva G, Andricopulo AD, Wainer IW, Cass QB. The development of an immobilized enzyme reactor containing glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzy: the effect of species' specific differences on the immobilization [Internet]. Analyst. 2008 ; 133( Ja 2008): 93-99.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1039/b711145b
Artigo de periodico
The three-dimensional structure of bothropasin, the main hemorrhagic factor from Bothrops jararaca venom: insights for a new classification of snake venom metalloprotease subgroups (2008)
Muniz, João Renato Carvalho ; Ambrosio, Andre Luis Berteli ; Araújo, Heloisa Sobreiro Selistre de; Cominetti, Márcia R.; Silva, Ana M. Moura; Oliva, Glaucius ; Garratt, Richard Charles ; Souza, Dulce H. F.
Source: Toxicon. Unidade: IFSC
Subjects: TOXINAS, VENENOS DE ORIGEM ANIMAL, COBRAS, PROTEÍNAS, ENZIMAS, CRISTALOGRAFIA DE RAIOS X
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ABNT
MUNIZ, João Renato Carvalho et al. The three-dimensional structure of bothropasin, the main hemorrhagic factor from Bothrops jararaca venom: insights for a new classification of snake venom metalloprotease subgroups. Toxicon, v. 52, n. 7, p. 807-816, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2008.08.021. Acesso em: 15 nov. 2024.
APA
Muniz, J. R. C., Ambrosio, A. L. B., Araújo, H. S. S. de, Cominetti, M. R., Silva, A. M. M., Oliva, G., et al. (2008). The three-dimensional structure of bothropasin, the main hemorrhagic factor from Bothrops jararaca venom: insights for a new classification of snake venom metalloprotease subgroups. Toxicon, 52( 7), 807-816. doi:10.1016/j.toxicon.2008.08.021
NLM
Muniz JRC, Ambrosio ALB, Araújo HSS de, Cominetti MR, Silva AMM, Oliva G, Garratt RC, Souza DHF. The three-dimensional structure of bothropasin, the main hemorrhagic factor from Bothrops jararaca venom: insights for a new classification of snake venom metalloprotease subgroups [Internet]. Toxicon. 2008 ; 52( 7): 807-816.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.toxicon.2008.08.021
Vancouver
Muniz JRC, Ambrosio ALB, Araújo HSS de, Cominetti MR, Silva AMM, Oliva G, Garratt RC, Souza DHF. The three-dimensional structure of bothropasin, the main hemorrhagic factor from Bothrops jararaca venom: insights for a new classification of snake venom metalloprotease subgroups [Internet]. Toxicon. 2008 ; 52( 7): 807-816.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.toxicon.2008.08.021
Artigo de periodico
Anacardic acid derivatives as inhibitors of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi (2008)
Pereira, Junia M.; Severino, Richele P.; Vieira, Paulo C.; Fernandes, João B.; Silva, Maria de Fátima G. F.; Zottis, Anderson; Andricopulo, Adriano Defini ; Oliva, Glaucius ; Corrêa, Arlene G.
Source: Bioorganic & Medicinal Chemistry. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS (PREVENÇÃO E CONTROLE), ENZIMAS (ESTUDO), INIBIDORES DE ENZIMAS, TRYPANOSOMA CRUZI, DOENÇAS PARASITÁRIAS
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ABNT
PEREIRA, Junia M. et al. Anacardic acid derivatives as inhibitors of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi. Bioorganic & Medicinal Chemistry, v. 16, n. 19, p. 8889-8895, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2008.08.057. Acesso em: 15 nov. 2024.
APA
Pereira, J. M., Severino, R. P., Vieira, P. C., Fernandes, J. B., Silva, M. de F. G. F., Zottis, A., et al. (2008). Anacardic acid derivatives as inhibitors of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi. Bioorganic & Medicinal Chemistry, 16( 19), 8889-8895. doi:10.1016/j.bmc.2008.08.057
NLM
Pereira JM, Severino RP, Vieira PC, Fernandes JB, Silva M de FGF, Zottis A, Andricopulo AD, Oliva G, Corrêa AG. Anacardic acid derivatives as inhibitors of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi [Internet]. Bioorganic & Medicinal Chemistry. 2008 ; 16( 19): 8889-8895.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2008.08.057
Vancouver
Pereira JM, Severino RP, Vieira PC, Fernandes JB, Silva M de FGF, Zottis A, Andricopulo AD, Oliva G, Corrêa AG. Anacardic acid derivatives as inhibitors of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi [Internet]. Bioorganic & Medicinal Chemistry. 2008 ; 16( 19): 8889-8895.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2008.08.057
Artigo de periodico
Biological activities from extracts of endophytic fungi isolated from Viguiera arenaria and Tithonia diversifolia (2008)
Guimarães, Denise O.; Borges, Warley S.; Kawano, Cristina Y.; Ribeiro, Patrícia H.; Goldman, Gustavo H.; Nomizo, Auro; Thiemann, Otávio Henrique ; Oliva, Glaucius ; Lopes, Norberto Peporine; Pupo, Mônica Tallarico
Source: FEMS Immunology and Medical Microbiology. Unidades: IFSC, FCFRP
Subjects: PRODUTOS NATURAIS, BIOTECNOLOGIA, FARMACOBOTÂNICA, FUNGOS
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ABNT
GUIMARÃES, Denise O. et al. Biological activities from extracts of endophytic fungi isolated from Viguiera arenaria and Tithonia diversifolia. FEMS Immunology and Medical Microbiology, v. 52, n. 1, p. 134-144, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1574-695x.2007.00354.x. Acesso em: 15 nov. 2024.
APA
Guimarães, D. O., Borges, W. S., Kawano, C. Y., Ribeiro, P. H., Goldman, G. H., Nomizo, A., et al. (2008). Biological activities from extracts of endophytic fungi isolated from Viguiera arenaria and Tithonia diversifolia. FEMS Immunology and Medical Microbiology, 52( 1), 134-144. doi:10.1111/j.1574-695x.2007.00354.x
NLM
Guimarães DO, Borges WS, Kawano CY, Ribeiro PH, Goldman GH, Nomizo A, Thiemann OH, Oliva G, Lopes NP, Pupo MT. Biological activities from extracts of endophytic fungi isolated from Viguiera arenaria and Tithonia diversifolia [Internet]. FEMS Immunology and Medical Microbiology. 2008 ; 52( 1): 134-144.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1574-695x.2007.00354.x
Vancouver
Guimarães DO, Borges WS, Kawano CY, Ribeiro PH, Goldman GH, Nomizo A, Thiemann OH, Oliva G, Lopes NP, Pupo MT. Biological activities from extracts of endophytic fungi isolated from Viguiera arenaria and Tithonia diversifolia [Internet]. FEMS Immunology and Medical Microbiology. 2008 ; 52( 1): 134-144.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1574-695x.2007.00354.x
Artigo de periodico
Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi (2008)
Guido, Rafael Victorio Carvalho ; Trossini, Gustavo Henrique Goulart ; Castilho, Marcelo S.; Oliva, Glaucius ; Ferreira, Elizabeth Igne ; Andricopulo, Adriano Defini
Source: Journal of Enzyme Inhibition and Medicinal Chemistry. Unidades: IFSC, FCF
Subjects: INIBIDORES DE ENZIMAS, DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS, QUIMIOTERAPIA, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, TRYPANOSOMA CRUZI
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ABNT
GUIDO, Rafael Victorio Carvalho et al. Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi. Journal of Enzyme Inhibition and Medicinal Chemistry, v. 23, n. 6, p. 964-973, 2008Tradução . . Disponível em: https://doi.org/10.1080/14756360701810322. Acesso em: 15 nov. 2024.
APA
Guido, R. V. C., Trossini, G. H. G., Castilho, M. S., Oliva, G., Ferreira, E. I., & Andricopulo, A. D. (2008). Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi. Journal of Enzyme Inhibition and Medicinal Chemistry, 23( 6), 964-973. doi:10.1080/14756360701810322
NLM
Guido RVC, Trossini GHG, Castilho MS, Oliva G, Ferreira EI, Andricopulo AD. Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2008 ; 23( 6): 964-973.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1080/14756360701810322
Vancouver
Guido RVC, Trossini GHG, Castilho MS, Oliva G, Ferreira EI, Andricopulo AD. Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2008 ; 23( 6): 964-973.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1080/14756360701810322
Artigo de periodico
Crystal structure of Leishmania tarentolae hypoxanthine-guanine phosphoribosyltransferase (2007)
Monzani, Paulo S.; Trapani, Stefano; Thiemann, Otávio Henrique ; Oliva, Glaucius
Source: BMC Structural Biology. Unidade: IFSC
Subjects: LEISHMANIA, PROTEÍNAS (MODELOS), CRISTALOGRAFIA FÍSICA
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ABNT
MONZANI, Paulo S. et al. Crystal structure of Leishmania tarentolae hypoxanthine-guanine phosphoribosyltransferase. BMC Structural Biology, v. 7, n. 59, p. Se 2007, 2007Tradução . . Disponível em: https://doi.org/10.1186/1472-6807-7-59. Acesso em: 15 nov. 2024.
APA
Monzani, P. S., Trapani, S., Thiemann, O. H., & Oliva, G. (2007). Crystal structure of Leishmania tarentolae hypoxanthine-guanine phosphoribosyltransferase. BMC Structural Biology, 7( 59), Se 2007. doi:10.1186/1472-6807-7-59
NLM
Monzani PS, Trapani S, Thiemann OH, Oliva G. Crystal structure of Leishmania tarentolae hypoxanthine-guanine phosphoribosyltransferase [Internet]. BMC Structural Biology. 2007 ; 7( 59): Se 2007.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1472-6807-7-59
Vancouver
Monzani PS, Trapani S, Thiemann OH, Oliva G. Crystal structure of Leishmania tarentolae hypoxanthine-guanine phosphoribosyltransferase [Internet]. BMC Structural Biology. 2007 ; 7( 59): Se 2007.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1472-6807-7-59
Editor de periodico
Acta Crystallographica D (2007)
Kostorz, G. (Editor); Oliva, Glaucius (Editor)
Unidade: IFSC
Subjects: CRISTALOGRAFIA, BIOLOGIA (ESTRUTURA), PROTEÍNAS
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ABNT
Acta Crystallographica D. . Oxford: Blackwell Publishing. . Acesso em: 15 nov. 2024. , 2007
APA
Acta Crystallographica D. (2007). Acta Crystallographica D. Oxford: Blackwell Publishing.
NLM
Acta Crystallographica D. 2007 ;[citado 2024 nov. 15 ]
Vancouver
Acta Crystallographica D. 2007 ;[citado 2024 nov. 15 ]
Artigo de periodico
Structural analysis of N-acetylglucosamine-6-phosphate deacetylase apoenzime from Escherichia coli (2006)
Ferreira, Frederico Moraes; Mendoza-Hernandez, Guillermo; Castãneda-Bueno, Maria; Aparicio, Ricardo; Fischer, Hannes; Calcagno, Mário L.; Oliva, Glaucius
Source: Journal of Molecular Biology. Unidade: IFSC
Subjects: ESCHERICHIA COLI, ENZIMAS, CRISTALOGRAFIA FÍSICA (ESTRUTURA), AÇÚCAR, AMINOÁCIDOS
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ABNT
FERREIRA, Frederico Moraes et al. Structural analysis of N-acetylglucosamine-6-phosphate deacetylase apoenzime from Escherichia coli. Journal of Molecular Biology, v. 359, n. Ju 2006, p. 308-321, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jmb.2006.03.024. Acesso em: 15 nov. 2024.
APA
Ferreira, F. M., Mendoza-Hernandez, G., Castãneda-Bueno, M., Aparicio, R., Fischer, H., Calcagno, M. L., & Oliva, G. (2006). Structural analysis of N-acetylglucosamine-6-phosphate deacetylase apoenzime from Escherichia coli. Journal of Molecular Biology, 359( Ju 2006), 308-321. doi:10.1016/j.jmb.2006.03.024
NLM
Ferreira FM, Mendoza-Hernandez G, Castãneda-Bueno M, Aparicio R, Fischer H, Calcagno ML, Oliva G. Structural analysis of N-acetylglucosamine-6-phosphate deacetylase apoenzime from Escherichia coli [Internet]. Journal of Molecular Biology. 2006 ; 359( Ju 2006): 308-321.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.jmb.2006.03.024
Vancouver
Ferreira FM, Mendoza-Hernandez G, Castãneda-Bueno M, Aparicio R, Fischer H, Calcagno ML, Oliva G. Structural analysis of N-acetylglucosamine-6-phosphate deacetylase apoenzime from Escherichia coli [Internet]. Journal of Molecular Biology. 2006 ; 359( Ju 2006): 308-321.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.jmb.2006.03.024
Artigo de periodico
Two- and three-dimensional quantitative structure-activity relationships for a series of purine nucleoside phosphorylase inhibitors (2006)
Castilho, Marcelo Santos; Postigo, Matheus Pereira; Paula, Caroline B. V. de; Montanari, Carlos Alberto ; Oliva, Glaucius ; Andricopulo, Adriano Defini
Source: Bioorganic & Medicinal Chemistry. Unidades: IQSC, IFSC
Subjects: QUÍMICA MÉDICA, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
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ABNT
CASTILHO, Marcelo Santos et al. Two- and three-dimensional quantitative structure-activity relationships for a series of purine nucleoside phosphorylase inhibitors. Bioorganic & Medicinal Chemistry, v. 14, n. Ja 2006, p. 516-527, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2005.08.055. Acesso em: 15 nov. 2024.
APA
Castilho, M. S., Postigo, M. P., Paula, C. B. V. de, Montanari, C. A., Oliva, G., & Andricopulo, A. D. (2006). Two- and three-dimensional quantitative structure-activity relationships for a series of purine nucleoside phosphorylase inhibitors. Bioorganic & Medicinal Chemistry, 14( Ja 2006), 516-527. doi:10.1016/j.bmc.2005.08.055
NLM
Castilho MS, Postigo MP, Paula CBV de, Montanari CA, Oliva G, Andricopulo AD. Two- and three-dimensional quantitative structure-activity relationships for a series of purine nucleoside phosphorylase inhibitors [Internet]. Bioorganic & Medicinal Chemistry. 2006 ; 14( Ja 2006): 516-527.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2005.08.055
Vancouver
Castilho MS, Postigo MP, Paula CBV de, Montanari CA, Oliva G, Andricopulo AD. Two- and three-dimensional quantitative structure-activity relationships for a series of purine nucleoside phosphorylase inhibitors [Internet]. Bioorganic & Medicinal Chemistry. 2006 ; 14( Ja 2006): 516-527.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2005.08.055
Editor de periodico
Acta Crystallographica. D, Biological Crystallography (2006)
Kostorz, G. (Editor); Oliva, Glaucius (Editor)
Unidade: IFSC
Subjects: CRISTALOGRAFIA, BIOLOGIA
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ABNT
Acta Crystallographica. D, Biological Crystallography. . Oxford: Blackwell Publishing. . Acesso em: 15 nov. 2024. , 2006
APA
Acta Crystallographica. D, Biological Crystallography. (2006). Acta Crystallographica. D, Biological Crystallography. Oxford: Blackwell Publishing.
NLM
Acta Crystallographica. D, Biological Crystallography. 2006 ;[citado 2024 nov. 15 ]
Vancouver
Acta Crystallographica. D, Biological Crystallography. 2006 ;[citado 2024 nov. 15 ]
Artigo de periodico
Preliminary crystalographic analysis of sugar cane phosphoribosylpyrophosphate synthase (2005)
Napolitano, Hamilton B.; Sculaccio, Susana Andréa; Thiemann, Otávio Henrique ; Oliva, Glaucius
Source: Acta Crystallographica F. Unidade: IFSC
Subjects: CRISTALIZAÇÃO, ENZIMAS, CANA-DE-AÇÚCAR, DIFRAÇÃO POR RAIOS X, CRISTALOGRAFIA, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAPOLITANO, Hamilton B. et al. Preliminary crystalographic analysis of sugar cane phosphoribosylpyrophosphate synthase. Acta Crystallographica F, v. 61, n. Ja 2005, p. 49-51, 2005Tradução . . Disponível em: https://doi.org/10.1107/s1744309104025825. Acesso em: 15 nov. 2024.
APA
Napolitano, H. B., Sculaccio, S. A., Thiemann, O. H., & Oliva, G. (2005). Preliminary crystalographic analysis of sugar cane phosphoribosylpyrophosphate synthase. Acta Crystallographica F, 61( Ja 2005), 49-51. doi:10.1107/s1744309104025825
NLM
Napolitano HB, Sculaccio SA, Thiemann OH, Oliva G. Preliminary crystalographic analysis of sugar cane phosphoribosylpyrophosphate synthase [Internet]. Acta Crystallographica F. 2005 ; 61( Ja 2005): 49-51.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1107/s1744309104025825
Vancouver
Napolitano HB, Sculaccio SA, Thiemann OH, Oliva G. Preliminary crystalographic analysis of sugar cane phosphoribosylpyrophosphate synthase [Internet]. Acta Crystallographica F. 2005 ; 61( Ja 2005): 49-51.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1107/s1744309104025825
Editor de periodico
Acta Crystallographica. D, Biological Crystallography (2005)
Helliwell, J. R. (Editor); Oliva, Glaucius (Editor)
Unidade: IFSC
Subjects: CRISTALOGRAFIA, BIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
Acta Crystallographica. D, Biological Crystallography. . Oxford: Blackwell Publishing. . Acesso em: 15 nov. 2024. , 2005
APA
Acta Crystallographica. D, Biological Crystallography. (2005). Acta Crystallographica. D, Biological Crystallography. Oxford: Blackwell Publishing.
NLM
Acta Crystallographica. D, Biological Crystallography. 2005 ;[citado 2024 nov. 15 ]
Vancouver
Acta Crystallographica. D, Biological Crystallography. 2005 ;[citado 2024 nov. 15 ]
Artigo de periodico
New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi (2004)
Marchi, Anderson Aparecido de; Castilho, Marcelo Santos; Nascimento, Paulo Gustavo Barboni; Archanjo, Fernando Costa; Del Ponte, Gino; Oliva, Glaucius ; Pupo, Mônica Tallarico
Source: Bioorganic & Medicinal Chemistry. Unidades: FCFRP, IFSC
Subjects: ENZIMAS, TRYPANOSOMA CRUZI, PROTOZOA, PARASITISMO, CRISTALOGRAFIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARCHI, Anderson Aparecido de et al. New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi. Bioorganic & Medicinal Chemistry, v. 12, n. 18, p. Se 2004, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2004.07.018. Acesso em: 15 nov. 2024.
APA
Marchi, A. A. de, Castilho, M. S., Nascimento, P. G. B., Archanjo, F. C., Del Ponte, G., Oliva, G., & Pupo, M. T. (2004). New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi. Bioorganic & Medicinal Chemistry, 12( 18), Se 2004. doi:10.1016/j.bmc.2004.07.018
NLM
Marchi AA de, Castilho MS, Nascimento PGB, Archanjo FC, Del Ponte G, Oliva G, Pupo MT. New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi [Internet]. Bioorganic & Medicinal Chemistry. 2004 ; 12( 18): Se 2004.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2004.07.018
Vancouver
Marchi AA de, Castilho MS, Nascimento PGB, Archanjo FC, Del Ponte G, Oliva G, Pupo MT. New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi [Internet]. Bioorganic & Medicinal Chemistry. 2004 ; 12( 18): Se 2004.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2004.07.018
Artigo de periodico
Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase (2004)
Leitão, Andrei ; Andricopulo, Adriano Defini ; Oliva, Glaucius ; Pupo, Mônica Tallarico; Marchi, Anderson A. de; Vieira, Paulo C.; Silva, Maria Fatima G. F. da; Ferreira, Vitor F.; Souza, Maria Cecília B. V. de; Sá, Marcus M.; Moraes, Valéria R. S.; Montanari, Carlos Alberto
Source: Bioorganic & Medicinal Chemistry Letters. Unidades: IFSC, FCFRP
Subjects: ENZIMAS, TRYPANOSOMA CRUZI, PROTOZOA, PARASITISMO, CRISTALOGRAFIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEITÃO, Andrei et al. Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase. Bioorganic & Medicinal Chemistry Letters, v. 14, n. 9, p. 2199-2204, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2004.02.025. Acesso em: 15 nov. 2024.
APA
Leitão, A., Andricopulo, A. D., Oliva, G., Pupo, M. T., Marchi, A. A. de, Vieira, P. C., et al. (2004). Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase. Bioorganic & Medicinal Chemistry Letters, 14( 9), 2199-2204. doi:10.1016/j.bmcl.2004.02.025
NLM
Leitão A, Andricopulo AD, Oliva G, Pupo MT, Marchi AA de, Vieira PC, Silva MFGF da, Ferreira VF, Souza MCBV de, Sá MM, Moraes VRS, Montanari CA. Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2004 ; 14( 9): 2199-2204.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmcl.2004.02.025
Vancouver
Leitão A, Andricopulo AD, Oliva G, Pupo MT, Marchi AA de, Vieira PC, Silva MFGF da, Ferreira VF, Souza MCBV de, Sá MM, Moraes VRS, Montanari CA. Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2004 ; 14( 9): 2199-2204.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmcl.2004.02.025
Artigo de periodico
Crystal structure Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase complexed with an analogue of 1,3-bisphospho-D-plyceric acid: selective inhibition by structure-based design (2003)
Ladame, Sylvain; Castilho, Marcelo S.; Silva, Carlos H. T. P.; Denier, Colette; Hannaert, Véronique; Périé Jacques; Oliva, Glaucius ; Willson, Michèle
Source: European Journal of Biochemistry. Unidade: IFSC
Subjects: CRISTALOGRAFIA, TRYPANOSOMA CRUZI, ENZIMAS, PROTEÍNAS (MODELOS), LEISHMANIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LADAME, Sylvain et al. Crystal structure Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase complexed with an analogue of 1,3-bisphospho-D-plyceric acid: selective inhibition by structure-based design. European Journal of Biochemistry, v. No 2003, n. 22, p. 4574-4586, 2003Tradução . . Disponível em: https://doi.org/10.1046/j.1432-1033.2003.03857.x. Acesso em: 15 nov. 2024.
APA
Ladame, S., Castilho, M. S., Silva, C. H. T. P., Denier, C., Hannaert, V., Périé Jacques,, et al. (2003). Crystal structure Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase complexed with an analogue of 1,3-bisphospho-D-plyceric acid: selective inhibition by structure-based design. European Journal of Biochemistry, No 2003( 22), 4574-4586. doi:10.1046/j.1432-1033.2003.03857.x
NLM
Ladame S, Castilho MS, Silva CHTP, Denier C, Hannaert V, Périé Jacques, Oliva G, Willson M. Crystal structure Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase complexed with an analogue of 1,3-bisphospho-D-plyceric acid: selective inhibition by structure-based design [Internet]. European Journal of Biochemistry. 2003 ; No 2003( 22): 4574-4586.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1046/j.1432-1033.2003.03857.x
Vancouver
Ladame S, Castilho MS, Silva CHTP, Denier C, Hannaert V, Périé Jacques, Oliva G, Willson M. Crystal structure Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase complexed with an analogue of 1,3-bisphospho-D-plyceric acid: selective inhibition by structure-based design [Internet]. European Journal of Biochemistry. 2003 ; No 2003( 22): 4574-4586.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1046/j.1432-1033.2003.03857.x

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