Curated Information
Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage Cell Signaling Technology
PhosphoSitePlus
HomeAbout PhosphoSiteUsing PhosphoSiteCuration ProcessContact
NIH-logos NIGMS Logo NIAAA Logo NCI Logo NIH Logo
Curated Information Page
PubMed Id: 9199329 
Krstic MD, Rogatsky I, Yamamoto KR, Garabedian MJ (1997) Mitogen-activated and cyclin-dependent protein kinases selectively and differentially modulate transcriptional enhancement by the glucocorticoid receptor. Mol Cell Biol 17, 3947-54 9199329
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, 2012,40:D261-70). To learn more about the scope of PhosphoSitePlus®, click here.
Only sites from this record are displayed on this page. Click on the protein name to open the protein page, and on the RSD number to open the site page. For the complete dataset, click the download button, on the right.
Download Sites

T171-p - GR (rat)
Orthologous residues
GR (human): A150‑p, GR iso2 (human): A150‑p, GR (mouse): T159‑p, GR (rat): T171‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  hepatic
 Cellular systems studied:  primary cells
 Species studied:  rat
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE ERK2 (rat)

S224-p - GR (rat)
Orthologous residues
GR (human): S203‑p, GR iso2 (human): S203‑p, GR (mouse): S212‑p, GR (rat): S224‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  hepatic
 Cellular systems studied:  primary cells
 Species studied:  rat
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE CDK2 (human)
 Comments:  Cyclin A-Cdk2 complex is responsible for this phosphorylation.

S232-p - GR (rat)
Orthologous residues
GR (human): S211‑p, GR iso2 (human): S211‑p, GR (mouse): S220‑p, GR (rat): S232‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  hepatic
 Cellular systems studied:  primary cells
 Species studied:  rat
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE CDK2 (human)
 Comments:  Cyclin A-Cdk2 complex is responsible for this phosphorylation

S246-p - GR (rat)
Orthologous residues
GR (human): S226‑p, GR iso2 (human): S226‑p, GR (mouse): S234‑p, GR (rat): S246‑p
Characterization
 Methods used to characterize site in vivo [32P] bio-synthetic labeling, phosphopeptide mapping
 Relevant cell lines - cell types - tissues:  hepatic
 Cellular systems studied:  primary cells
 Species studied:  rat
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE ERK2 (rat)


Home  |  Curator Login With enhanced literature mining using Linguamatics I2E I2E Logo Produced by 3rd Millennium  |  Design by Digizyme
©2003-2013 Cell Signaling Technology, Inc.