Please use this identifier to cite or link to this item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/9296
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dc.contributor.authorFERRAZ, L. F. C.
dc.contributor.authorSOARDI, F.
dc.contributor.authorFALCÃO, P.
dc.contributor.authorNESHICH, G.
dc.contributor.authorMELLO, M. P. de
dc.date.accessioned2022-05-17T18:13:32Z-
dc.date.available2022-05-17T18:13:32Z-
dc.date.created2006-08-17
dc.date.issued2006
dc.identifier.citationIn: ANNUAL INTERNATIONAL CONFERENCE ON INTELLIGENT SYSTEMS FOR MOLECULAR BIOLOGY, 14.; ANNUAL AB3C CONFERENCE, 2., 2006, Fortaleza. Conference Program... Fortaleza: ISCB, 2006.
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/9296-
dc.descriptionShort abstract: We describe the mutation Pro222GIn in HSD3B2 gene on a patient with congenital adrenal hyperplasia. Molecular modeling of 3B-HSD2 mutant allowed us to identify critical role of residue Pro222 on the folding pattern and catalytic activity of the enzyme. The proposed models correlate with the experimental data previously reported.
dc.language.isoeng
dc.rightsopenAccess
dc.subjectMutação gênica
dc.subjectHiperplasia adrenal congenital
dc.subjectModelagem molecular
dc.titleMolecular homologous modeling of 3B-HSD2 mutant enzyme: structure-function aspects of Pro222GLN mutation correlates with the experimental data from a patient with congenital adrenal hyperplasia.
dc.typeResumo em anais e proceedings
dc.subject.thesagroBiologia molecular
dc.subject.nalthesaurusMutation
dc.subject.nalthesaurusHyperplasia
dc.subject.nalthesaurusMolecular Biology
dc.description.notesISMB, X-MEETING 2006. Poster D-12.
dc.format.extent2Não paginado.
riaa.ainfo.id9296
riaa.ainfo.lastupdate2022-05-17
dc.contributor.institutionLUCIO FABIO CALDAS FERRAZ, CBMEG/Unicamp; FERNANDA SOARDI, CBMEG/Unicamp; PAULA REGINA KUSER FALCAO, CNPTIA; GORAN NESHICH, CNPTIA; MARICILDA PALANDI DE MELLO, CBMEG/Unicamp.
Appears in Collections:Resumo em anais de congresso (CNPTIA)

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