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Refinement and prediction of protein prenylation motifs

We refined the motifs for carboxy-terminal protein prenylation by analysis of known substrates for farnesyltransferase (FT), geranylgeranyltransferase I (GGT1) and geranylgeranyltransferase II (GGT2). In addition to the CaaX box for the first two enzymes, we identify a preceding linker region that a...

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Detalles Bibliográficos
Autores principales: Maurer-Stroh, Sebastian, Eisenhaber, Frank
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175975/
https://www.ncbi.nlm.nih.gov/pubmed/15960807
http://dx.doi.org/10.1186/gb-2005-6-6-r55
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author Maurer-Stroh, Sebastian
Eisenhaber, Frank
author_facet Maurer-Stroh, Sebastian
Eisenhaber, Frank
author_sort Maurer-Stroh, Sebastian
collection PubMed
description We refined the motifs for carboxy-terminal protein prenylation by analysis of known substrates for farnesyltransferase (FT), geranylgeranyltransferase I (GGT1) and geranylgeranyltransferase II (GGT2). In addition to the CaaX box for the first two enzymes, we identify a preceding linker region that appears constrained in physicochemical properties, requiring small or flexible, preferably hydrophilic, amino acids. Predictors were constructed on the basis of sequence and physical property profiles, including interpositional correlations, and are available as the Prenylation Prediction Suite (PrePS, ) which also allows evaluation of evolutionary motif conservation. PrePS can predict partially overlapping substrate specificities, which is of medical importance in the case of understanding cellular action of FT inhibitors as anticancer and anti-parasite agents.
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spelling pubmed-11759752005-07-17 Refinement and prediction of protein prenylation motifs Maurer-Stroh, Sebastian Eisenhaber, Frank Genome Biol Software We refined the motifs for carboxy-terminal protein prenylation by analysis of known substrates for farnesyltransferase (FT), geranylgeranyltransferase I (GGT1) and geranylgeranyltransferase II (GGT2). In addition to the CaaX box for the first two enzymes, we identify a preceding linker region that appears constrained in physicochemical properties, requiring small or flexible, preferably hydrophilic, amino acids. Predictors were constructed on the basis of sequence and physical property profiles, including interpositional correlations, and are available as the Prenylation Prediction Suite (PrePS, ) which also allows evaluation of evolutionary motif conservation. PrePS can predict partially overlapping substrate specificities, which is of medical importance in the case of understanding cellular action of FT inhibitors as anticancer and anti-parasite agents. BioMed Central 2005 2005-05-27 /pmc/articles/PMC1175975/ /pubmed/15960807 http://dx.doi.org/10.1186/gb-2005-6-6-r55 Text en Copyright © 2005 Maurer-Stroh and Eisenhaber; licensee BioMed Central Ltd.
spellingShingle Software
Maurer-Stroh, Sebastian
Eisenhaber, Frank
Refinement and prediction of protein prenylation motifs
title Refinement and prediction of protein prenylation motifs
title_full Refinement and prediction of protein prenylation motifs
title_fullStr Refinement and prediction of protein prenylation motifs
title_full_unstemmed Refinement and prediction of protein prenylation motifs
title_short Refinement and prediction of protein prenylation motifs
title_sort refinement and prediction of protein prenylation motifs
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175975/
https://www.ncbi.nlm.nih.gov/pubmed/15960807
http://dx.doi.org/10.1186/gb-2005-6-6-r55
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