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Mars -- robust automatic backbone assignment of proteins.
Jung, Young-Sang; Zweckstetter, Markus.
Afiliação
  • Jung YS; Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, D-37077 Göttingen, Germany.
J Biomol NMR ; 30(1): 11-23, 2004 Sep.
Article em En | MEDLINE | ID: mdl-15452431
MARS a program for robust automatic backbone assignment of (13)C/(15)N labeled proteins is presented. MARS does not require tight thresholds for establishing sequential connectivity or detailed adjustment of these thresholds and it can work with a wide variety of NMR experiments. Using only (13)C(alpha)/(13)C(beta) connectivity information, MARS allows automatic, error-free assignment of 96% of the 370-residue maltose-binding protein. MARS can successfully be used when data are missing for a substantial portion of residues or for proteins with very high chemical shift degeneracy such as partially or fully unfolded proteins. Other sources of information, such as residue specific information or known assignments from a homologues protein, can be included into the assignment process. MARS exports its result in SPARKY format. This allows visual validation and integration of automated and manual assignment.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas Idioma: En Revista: J Biomol NMR Assunto da revista: BIOLOGIA MOLECULAR / DIAGNOSTICO POR IMAGEM / MEDICINA NUCLEAR Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Alemanha
Buscar no Google
Base de dados: MEDLINE Assunto principal: Proteínas Idioma: En Revista: J Biomol NMR Assunto da revista: BIOLOGIA MOLECULAR / DIAGNOSTICO POR IMAGEM / MEDICINA NUCLEAR Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Alemanha