1AGR,1EZT


Conserved Protein Domain Family
RGS_RGS4

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cd08714: RGS_RGS4 
Click on image for an interactive view with Cn3D
Regulator of G protein signaling (RGS) domain found in the RGS4 protein
The RGS (Regulator of G-protein Signaling) domain is an essential part of the RGS4 protein. RGS4 is a member of the R4/RGS subfamily of the RGS family, a diverse group of multifunctional proteins that regulate cellular signaling events downstream of G-protein coupled receptors (GPCRs). As a major G-protein regulator, RGS domain containing proteins are involved in many crucial cellular processes such as regulation of intracellular trafficking, glial differentiation, embryonic axis formation, skeletal and muscle development, and cell migration during early embryogenesis. RGS proteins play critical regulatory roles as GTPase activating proteins (GAPs) of the heterotrimeric G-protein G-alpha subunits. The RGS domain controls G-protein signaling by accelerating the GTPase activity of the G-alpha subunit which leads to G protein deactivation and promotes desensitization. RGS4 is expressed widely in brain including prefrontal cortex, striatum, locus coeruleus (LC), and hippocampus and has been implicated in regulation of opioid, cholinergic, and serotonergic signaling. Dysfunctions in RGS4 proteins are involved in etiology of Parkinson's disease, addiction, and schizophrenia. RGS4 also is up-regulated in the failing human heart. RGS4 interacts with many binding partners outside of GPCR pathways, including calmodulin, COP, Kir3, PIP, calcium/CaM, PA, ErbB3, and 14-3-3.
Statistics
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PSSM-Id: 188669
Aligned: 6 rows
Threshold Bit Score: 198.567
Created: 15-May-2009
Updated: 2-Oct-2020
Structure
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Program:
Drawing:
Aligned Rows:
 
G-alpha-i1
Conserved site includes 10 residues -Click on image for an interactive view with Cn3D
Feature 1:G-alpha-i1 interaction site [polypeptide binding site]
Evidence:
  • Structure:1AGR_E: Homo sapiens RGS4 binds Gi-Alpha-1; contacts at 4 A
    View structure with Cn3D
  • Citation:PMID 9108480
  • Comment:RGS4 domain binds to the three switch regions of Gi-Alpha-1 and therefore catalyzes rapid hydrolysis of GTP primarily by stabilizing the switch regions.

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1                         ##  ##                                     # #  #  #        
1AGR_E     63 LENLINHEcGLAAFKAFLKSEYSEENIDFWISCEEYKkikspskLSPKAKKIYNEFIsvqatKEVNLDSCTREETSRnml 142 Norway rat
1EZT_A     17 LENLINHEcGLAAFKAFLKSEYSEENIDFWISCEEYKkikspskLSPKAKKIYNEFIsvqatKEVNLDSCTREETSRnml 96  Norway rat
NP_033088  63 LENLIHHEcGLAAFKAFLKSEYSEENIDFWISCEEYKkikspskLSPKAKKIYNEFIsvqatKEVNLDSCTREETSRnml 142 house mouse
NP_989716  63 LENLIHHDrGLAAFRAFLKSEYSEENIEFWVSCEDYKktkspakLSTKARKIYDEFIsvqatKEVNLDSCTREKTSHnml 142 chicken
Q6P300     64 LENLINNEcGLAAFRAFLQSEYSEENIDFWLACENYKkvktpekLLEKAQKIYEDFIsveatREVNLDSATREETSNnii 143 western clawed frog
Q6TEM0     71 FTNLIKNDdGRKAFASFLQSEYSQENIEFWVACEDFKqtp-adkMNLKARNIFERYIeadspREVNLDSVTREQTRKnle 149 zebrafish
Feature 1                     #   #             
1AGR_E    143 eptITCFDEAQKKIFNLMEkDSYRRFLKsRFYLD 176 Norway rat
1EZT_A     97 eptITCFDEAQKKIFNLMEkDSYRRFLKsRFYLD 130 Norway rat
NP_033088 143 qptITCFDEAQKKIFNLMEkDSYRRFLKsRFYLD 176 house mouse
NP_989716 143 eptLSCFDEAQRKIFTLMEkDSYRRFLK-SPYLD 175 chicken
Q6P300    144 qptHSTFDEAQHRIFILMEkDSYRRFLKsKFYLD 177 western clawed frog
Q6TEM0    150 mcdVSCFDEAQSKIFTLMEkDSYRRFLRsRLFLE 183 zebrafish

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