Home  |  Contact
PROSITE documentation PDOC51035 [for PROSITE entry PS51035]

BAG domain profile





Description

Bcl2-associated athanogene (BAG) family proteins participate in a wide variety of cellular processes including cell survival (stress response), proliferation, migration and apoptosis. These proteins share a conserved region of about 110 amino-acids at their carboxy terminus, named as the BAG domain. It has been shown [1,3] that the BAG domain can interact with the heat shock proteins 70 (Hsc70/Hsp70) (see <PDOC00269>) and can modulate either positively or negatively these chaperone proteins. In BAG-1, the BAG domain also interact with the serine/threonine kinase Raf-1 in a mutually exclusive interaction. BAG-1 promotes cell growth by binding to and stimulating Raf-1 activity. The binding to Hsc70/Hsp70 have an anti-apoptotic effect, it diminishes Raf-1 signaling and inhibits subsequent events, such as DNA synthesis and arrests of the cell cycle [1]. The C-terminus of the BAG domain is also a possible site of interaction with Bcl-2 in BAG-1 and BAG-3/CAIR-1 which provides a supra-additive anti-apoptotic effect [2].

The BAG domain is found in association with several N-terminal domains like ubiquitin (see <PDOC00271>), IQ (see <PDOC50096>), and the WW domain (see <PDOC50020>). These domains enable BAG family proteins to interact with other proteins and potentially alter the activity of those target proteins by recruiting Hsc70/Hsp70 [1].

The crystal structure of the BAG domain has been solved (see <PDB:1HX1>)[3], and revealed that it consists of three anti-parallel α helices. In the BAG domain the first and the second α-helices interact with the serine/threonine kinase Raf-1 and the second and third α-helices interact with the ATP-binding pocket of Hsc70/Hsp70.

The profile we developed covers half of the first α-helix, the second one and the third one.

Last update:

November 2004 / First entry.

-------------------------------------------------------------------------------

Technical section

PROSITE method (with tools and information) covered by this documentation:

BAG, PS51035; BAG domain profile  (MATRIX)


References

1AuthorsDoong H. Vrailas A. Kohn E.C.
TitleWhat's in the 'BAG'? -- a functional domain analysis of the BAG-family proteins.
SourceCancer Lett. 188:25-32(2002).
PubMed ID12406544

2AuthorsTakayama S. Sato T. Krajewski S. Kochel K. Irie S. Millan J.A. Reed J.C.
TitleCloning and functional analysis of BAG-1: a novel Bcl-2-binding protein with anti-cell death activity.
SourceCell 80:279-284(1995).
PubMed ID7834747

3AuthorsSondermann H. Scheufler C. Schneider C. Hoehfeld J. Hartl F.-U. Moarefi I.
TitleStructure of a Bag/Hsc70 complex: convergent functional evolution of Hsp70 nucleotide exchange factors.
SourceScience 291:1553-1557(2001).
PubMed ID11222862
DOI10.1126/science.291.5508.1553



PROSITE is copyrighted by the SIB Swiss Institute of Bioinformatics and distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives (CC BY-NC-ND 4.0) License, see prosite_license.html.

Miscellaneous

View entry in original PROSITE document format
View entry in raw text format (no links)