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RGS proteins: more than just GAPs for heterotrimeric G proteins
被引:176
作者:

De Vries, L
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Div Cellular & Mol Med, La Jolla, CA 92093 USA Univ Calif San Diego, Div Cellular & Mol Med, La Jolla, CA 92093 USA

Farquhar, MG
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Div Cellular & Mol Med, La Jolla, CA 92093 USA Univ Calif San Diego, Div Cellular & Mol Med, La Jolla, CA 92093 USA
机构:
[1] Univ Calif San Diego, Div Cellular & Mol Med, La Jolla, CA 92093 USA
关键词:
D O I:
10.1016/S0962-8924(99)01515-9
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Members of the newly described RGS family of proteins have a common RGS domain that contains GTPase-activating activity for many G alpha subunits of heterotrimeric G proteins. Their ability to dampen siganlling via G alpha(i)-, G alpha(q)- and G alpha(12/13)-coupled pathways makes them crucial players in mediating the multitude of cellular processes controlled by heterotrimeric G proteins. Some RGS proteins also contain additional motifs that link them to other signalling networks, where they constitute effector-type molecules. This review summarizes recent findings on RGS proteins, especially those that implicate RGS proteins in more than just enhancing the GTPase activity of their G alpha subunit targets.
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页码:138 / 144
页数:7
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