Active Sequences Collection (ASC) database: a new tool to assign functions to protein sequences

被引:22
作者
Facchiano, AM
Facchiano, A
Facchiano, F
机构
[1] CNR, Ist Sci Alimentaz, I-83100 Avellino, Italy
[2] IDI, I-00167 Rome, Italy
关键词
D O I
10.1093/nar/gkg042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Active Sequences Collection ( ASC) is a collection of amino acid sequences, with an unique feature: only short sequences are collected, with a demonstrated biological activity. The current version of ASC consists of three sections: DORRS, a collection of active RGD-containing peptides; TRANSIT, a collection of protein regions active as substrates of transglutaminase enzyme ( TGase), and BAC, a collection of short peptides with demonstrated biological activity. Literature references for each entry are reported, as well as cross references to other databases, when available. The current version of ASC includes more than 800 different entries. The main scope of this collection is to offer a new tool to investigate the structural features of protein active sites, additionally to similarity searches against large protein databases or searching for known functional patterns. ASC database is available at the web address http: / / crisceb. unina2. it/ ASC/ which also offers a dedicated query interface to compare user-defined protein sequences with the database, as well as an updating interface to allow contribution of new referenced active sequences.
引用
收藏
页码:379 / 382
页数:4
相关论文
共 31 条
  • [1] Glycoprotein IIb/IIIa antagonists induce apoptosis in rat cardiomyocytes by caspase-3 activation
    Adderley, SR
    Fitzgerald, DJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (08) : 5760 - 5766
  • [2] RGD peptide-induced apoptosis in human leukemia HL-60 cells requires caspase-3 activation
    Anuradha, CD
    Kanno, S
    Hirano, S
    [J]. CELL BIOLOGY AND TOXICOLOGY, 2000, 16 (05) : 275 - 283
  • [3] Tissue transglutaminase protects against apoptosis by modifying the tumor suppressor protein p110 Rb.
    Boehm, JE
    Singh, U
    Combs, C
    Antonyak, MA
    Cerione, RA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) : 20127 - 20130
  • [4] RGD peptides induce apoptosis by direct caspase-3 activation
    Buckley, CD
    Pilling, D
    Henriquez, NV
    Parsonage, G
    Threlfall, K
    Scheel-Toellner, D
    Simmons, DL
    Albar, AN
    Lord, JM
    Salmon, M
    [J]. NATURE, 1999, 397 (6719) : 534 - 539
  • [5] Inhibition of the alpha-ν integrins with a cyclic RGD peptide impairs angiogenesis, growth and metastasis of solid tumours in vivo
    Buerkle, MA
    Pahernik, SA
    Sutter, A
    Jonczyk, A
    Messmer, K
    Dellian, M
    [J]. BRITISH JOURNAL OF CANCER, 2002, 86 (05) : 788 - 795
  • [6] Tissue transglutaminase: an enzyme with a split personality
    Chen, JSK
    Mehta, K
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1999, 31 (08) : 817 - 836
  • [7] RGD-containing peptides trigger apoptosis in glomerular mesangial cells of adult human kidneys
    Chen, XM
    Wang, JZ
    Fu, B
    Yu, LF
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 234 (03) : 594 - 599
  • [8] Gene disruption of tissue transglutaminase
    De Laurenzi, V
    Melino, G
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (01) : 148 - 155
  • [9] Transglutaminase activity is involved in polyamine-induced programmed cell death
    Facchiano, F
    D'Arcangelo, D
    Riccomi, A
    Lentini, A
    Beninati, S
    Capogrossi, MC
    [J]. EXPERIMENTAL CELL RESEARCH, 2001, 271 (01) : 118 - 129
  • [10] BIOCHEMICAL EVENTS IN NATURALLY-OCCURRING FORMS OF CELL-DEATH
    FESUS, L
    [J]. FEBS LETTERS, 1993, 328 (1-2): : 1 - 5