Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 97, Issue 4, Pages 1483-1488Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.030409597
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Funding
- NEI NIH HHS [R01 EY011900, EY11900] Funding Source: Medline
- NLM NIH HHS [T15 LM007093, LM07093] Funding Source: Medline
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Proteins of the regulator of G protein signaling (RCS) family accelerate GTP hydrolysis by the or subunits (G(alpha)) of G proteins. leading to rapid recovery of signaling cascades. Many different RCS proteins can accelerate GTP hydrolysis by an individual G(alpha), and CTP hydrolysis rates of different G alpha(s) can be enhanced by the same RCS protein. Consequently, the mechanisms for specificity in RGS regulation and the residues involved remain unclear. Using the evolutionary trace (ET) method, we have identified a cluster of residues in the RGS domain that includes the RCS-C, binding interface and extends to include additional functionally important residues on the surface. One of these is within helix alpha 3, two are in alpha 5, and three are in the loop connecting alpha 5 and alpha 6. A cluster of surface residues on G(alpha) previously identified by ET, and composed predominantly of residues from the switch III region and helix alpha 3, is spatially contiguous with the PT-identified residues in the RGS domain. This cluster includes residues proposed to interact with the gamma subunit of G(t alpha)'s effector, cGMP phosphodiesterase (PDE gamma), The proximity of these clusters suggests that they form part of an interface between the effector and the RGS-G(alpha) complex. Sequence variations in these residues correlate with PDE gamma effects on GTPase acceleration. Because ET identifies residues important for all members of a protein family, these residues likely form a general site for regulation of G protein-coupled signaling cascades, possibly by means of effector interactions.
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