PAProC: a prediction algorithm for proteasomal cleavages available on the WWW

被引:146
作者
Nussbaum, AK [1 ]
Kuttler, C [1 ]
Hadeler, KP [1 ]
Rammensee, HG [1 ]
Schild, H [1 ]
机构
[1] Univ Tubingen, Interfak Inst Zellbiol, Immunol Abt, D-72076 Tubingen, Germany
关键词
proteasome; cleavage prediction; algorithm; MHC; CTL epitope;
D O I
10.1007/s002510100300
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The first version of PAProC (Prediction Algorithm for Proteasomal Cleavages) is now available to the general public. PAProC is a prediction tool for cleavages by human and yeast proteasomes, based on experimental cleavage data. It will be particularly useful for immunologists working on antigen processing and the prediction of major histocompatibility complex class I molecule (MHC I) ligands and cytotoxic T-lymphocyte (CTL) epitopes. Likewise, in cases in which proteasomal protein degradation has been indicated in disease, PAProC can be used to assess the general cleavability of disease-linked proteins. On its web site (http://www.paproc.de), background information and hyperlinks are provided for the user (e.g., to SYFPEITHI, the database for the prediction of MHC I ligands).
引用
收藏
页码:87 / 94
页数:8
相关论文
共 31 条
[1]   Abrogation of CTL epitope processing by single amino acid substitution flanking the C-terminal proteasome cleavage site [J].
Beekman, NJ ;
van Veelen, PA ;
van Hall, T ;
Neisig, A ;
Sijts, A ;
Camps, M ;
Kloetzel, PM ;
Neefjes, JJ ;
Melief, CJ ;
Ossendorp, F .
JOURNAL OF IMMUNOLOGY, 2000, 164 (04) :1898-1905
[2]   Role of the proteasome in Alzheimer's disease [J].
Checler, F ;
da Costa, CA ;
Ancolio, K ;
Chevallier, N ;
Lopez-Perez, E ;
Marambaud, P .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2000, 1502 (01) :133-138
[3]   Two distinct proteolytic processes in the generation of a major histocompatibility complex class I-presented peptide [J].
Craiu, A ;
Akoplan, T ;
Goldberg, A ;
Rock, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :10850-10855
[4]   Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1 [J].
Cummings, CJ ;
Mancini, MA ;
Antalffy, B ;
DeFranco, DB ;
Orr, HT ;
Zoghbi, HY .
NATURE GENETICS, 1998, 19 (02) :148-154
[5]   Inhibition of proteasomal degradation by the Gly-Ala repeat of Epstein-Barr virus is influenced by the length of the repeat and the strength of the degradation signal [J].
Dantuma, NP ;
Heessen, S ;
Lindsten, K ;
Jellne, M ;
Masucci, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8381-8385
[6]   PROCESSING OF MAJOR HISTOCOMPATIBILITY CLASS-I-RESTRICTED ANTIGENS IN THE ENDOPLASMIC-RETICULUM [J].
ELLIOTT, T ;
WILLIS, A ;
CERUNDOLO, V ;
TOWNSEND, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (04) :1481-1491
[7]   The human 26 S and 20 S proteasomes generate overlapping but different sets of peptide fragments from a model protein substrate [J].
Emmerich, NPN ;
Nussbaum, AK ;
Stevanovic, S ;
Priemer, M ;
Toes, REM ;
Rammensee, HG ;
Schild, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (28) :21140-21148
[8]   Cell death in polyglutamine diseases [J].
Evert, BO ;
Wüllner, U ;
Klockgether, T .
CELL AND TISSUE RESEARCH, 2000, 301 (01) :189-204
[9]   A theoretical approach towards the identification of cleavage-determining amino acid motifs of the 20 S proteasome. [J].
Holzhütter, HG ;
Frömmel, C ;
Kloetzel, PM .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 286 (04) :1251-1265
[10]   Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteins [J].
Krobitsch, S ;
Lindquist, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1589-1594