Curated Information
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Home > Curated Information Page > PubMed Id: 20463172
Gagnon KB, Delpire E (2010) On the substrate recognition and negative regulation of SPAK, a kinase modulating Na+-K+-2Cl- cotransport activity. Am J Physiol Cell Physiol 299, C614-20 20463172
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.
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T200-p - NKCC1 (mouse)
Modsite: YYDtHTNtYYLRtFG SwissProt Entrez-Gene
Orthologous residues
NKCC1 (human): T207‑p, NKCC1 iso3 (human): T207‑p, NKCC1 (mouse): T200‑p, NKCC1 (rat): T198‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Relevant cell lines - cell types - tissues:  oocyte
Cellular systems studied:  primary cells
Species studied:  frog
Downstream Regulation
Effect of modification (function):  activity, induced
Comments:  Enzymatic activation by SLK3 requires two threonines separated by 4 amino acids.

T205-p - NKCC1 (mouse)
Modsite: TNtYYLRtFGHNtMD SwissProt Entrez-Gene
Orthologous residues
NKCC1 (human): T212‑p, NKCC1 iso3 (human): T212‑p, NKCC1 (mouse): T205‑p, NKCC1 (rat): T203‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Relevant cell lines - cell types - tissues:  oocyte
Cellular systems studied:  primary cells
Species studied:  frog
Downstream Regulation
Effect of modification (function):  activity, induced
Comments:  Enzymatic activation by SLK3 requires two threonines separated by 4 amino acids.

T243-p - STLK3 (mouse)
Modsite: tRNKVRKtFVGtPCW SwissProt Entrez-Gene
Orthologous residues
STLK3 (human): T231‑p, STLK3 (mouse): T243‑p, STLK3 (rat): T240‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Relevant cell lines - cell types - tissues:  oocyte
Cellular systems studied:  primary cells
Species studied:  frog
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE WNK4 (mouse) mutation in upstream enzyme recognition motif, transfection of wild-type enzyme
Downstream Regulation
Effect of modification (function):  enzymatic activity, induced

S383-p - STLK3 (mouse)
Modsite: VRRVPGssGHLHKTE SwissProt Entrez-Gene
Orthologous residues
STLK3 (human): S371‑p, STLK3 (mouse): S383‑p, STLK3 (rat): S380‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Relevant cell lines - cell types - tissues:  oocyte
Cellular systems studied:  primary cells
Species studied:  frog
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE WNK4 (mouse) mutation in upstream enzyme recognition motif, transfection of wild-type enzyme
Downstream Regulation
Effect of modification (function):  enzymatic activity, induced