Curated Information
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Home > Curated Information Page > PubMed Id: 12417300
Yogo K, et al. (2002) Identification and functional analysis of novel phosphorylation sites in Cx43 in rat primary granulosa cells. FEBS Lett 531, 132-6 12417300
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
Information from this record has been curated, but not yet edited in PhosphoSitePlus® and may be incomplete.
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S365-p - GJA1 (rat)
Modsite: IVDQRPssRAssRAs SwissProt Entrez-Gene
Orthologous residues
GJA1 (human): S365‑p, GJA1 (mouse): S365‑p, GJA1 (rat): S365‑p, GJA1 (rabbit): S365‑p, GJA1 (pig): S365‑p, GJA1 (hamster): S365‑p, GJA1 (cow): S366‑p
Characterization
Methods used to characterize site in vivo [32P] bio-synthetic labeling, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
Relevant cell lines - cell types - tissues:  granulosa, HeLa (cervical)
Cellular systems studied:  cell lines, primary cells
Species studied:  human, rat
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
urofollitropin increase
Downstream Regulation
Effect of modification (function):  activity, induced
Comments:  gap junction/intercellular communication

S368-p - GJA1 (rat)
Modsite: QRPssRAssRAssRP SwissProt Entrez-Gene
Orthologous residues
GJA1 (human): S368‑p, GJA1 (mouse): S368‑p, GJA1 (rat): S368‑p, GJA1 (rabbit): S368‑p, GJA1 (pig): S368‑p, GJA1 (hamster): S368‑p, GJA1 (cow): S369‑p
Characterization
Methods used to characterize site in vivo [32P] bio-synthetic labeling, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
Relevant cell lines - cell types - tissues:  granulosa, HeLa (cervical)
Cellular systems studied:  cell lines, primary cells
Species studied:  human, rat
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
urofollitropin increase
Downstream Regulation
Effect of modification (function):  activity, induced
Comments:  gap junction/intercellular communication

S369-p - GJA1 (rat)
Modsite: RPssRAssRAssRPR SwissProt Entrez-Gene
Orthologous residues
GJA1 (human): S369‑p, GJA1 (mouse): S369‑p, GJA1 (rat): S369‑p, GJA1 (rabbit): S369‑p, GJA1 (pig): S369‑p, GJA1 (hamster): S369‑p, GJA1 (cow): S370‑p
Characterization
Methods used to characterize site in vivo [32P] bio-synthetic labeling, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
Relevant cell lines - cell types - tissues:  granulosa, HeLa (cervical)
Cellular systems studied:  cell lines, primary cells
Species studied:  human, rat
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
urofollitropin increase
Downstream Regulation
Effect of modification (function):  activity, induced
Comments:  gap junction/intercellular communication

S373-p - GJA1 (rat)
Modsite: RAssRAssRPRPDDL SwissProt Entrez-Gene
Orthologous residues
GJA1 (human): S373‑p, GJA1 (mouse): S373‑p, GJA1 (rat): S373‑p, GJA1 (rabbit): S373‑p, GJA1 (pig): S373‑p, GJA1 (hamster): S373‑p, GJA1 (cow): S374‑p
Characterization
Methods used to characterize site in vivo [32P] bio-synthetic labeling, mutation of modification site, phosphoamino acid analysis, phosphopeptide mapping
Relevant cell lines - cell types - tissues:  granulosa, HeLa (cervical)
Cellular systems studied:  cell lines, primary cells
Species studied:  human, rat
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
urofollitropin increase
Downstream Regulation
Effect of modification (function):  activity, induced
Comments:  gap junction/intercellular communication