2020
DOI: 10.1124/molpharm.120.000061
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N-Terminal Targeting of Regulator of G Protein Signaling Protein 2 for F-Box Only Protein 44–Mediated Proteasomal Degradation

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Cited by 5 publications
(2 citation statements)
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“…However, FBXO44 is only capable of targeting RGS2 for ubiquitination in the context of CUL4B but not CUL1 [140]. The RGS2-FBXO44 interaction can be regulated by phosphorylation, and the phosphorylation of Ser 3 on RGS2 could protect RGS2 from degradation through reducing its binding with FBXO44 [145]. Since low RGS2 protein level is associated with disease such as hypertension and heart failure, drugs that interfere with the RGS2-FBXO44 interaction can be beneficial for preventing cardiovascular diseases [145].…”
Section: Non-canonical Crl4s Involved In Cardiovascular Diseasesmentioning
confidence: 99%
“…However, FBXO44 is only capable of targeting RGS2 for ubiquitination in the context of CUL4B but not CUL1 [140]. The RGS2-FBXO44 interaction can be regulated by phosphorylation, and the phosphorylation of Ser 3 on RGS2 could protect RGS2 from degradation through reducing its binding with FBXO44 [145]. Since low RGS2 protein level is associated with disease such as hypertension and heart failure, drugs that interfere with the RGS2-FBXO44 interaction can be beneficial for preventing cardiovascular diseases [145].…”
Section: Non-canonical Crl4s Involved In Cardiovascular Diseasesmentioning
confidence: 99%
“…Regulators of G protein signaling (RGS) are a group of regulator proteins of G protein‐coupled receptors. RGS proteins are accelerator proteins of GTPase, which turn off the signal transduction of Gα and βγ of G protein and negatively regulate G protein signaling (McNabb et al., 2020; Senese et al., 2020). So far, there are more than 20 RGS proteins, which are abundantly expressed in many brain regions that mediate addiction and analgesia.…”
Section: Introductionmentioning
confidence: 99%