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Orthologous residues
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CDK9 (human): S175‑p, CDK9 iso2 (human): S292‑p, CDK9 (mouse): S175‑p, CDK9 (rat): S175‑p
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Characterization
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Methods used to characterize site in vivo:
[32P] bio-synthetic labeling, immunoprecipitation, mass spectrometry, mutation of modification site, phosphopeptide mapping
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Relevant cell lines - cell types - tissues:
293T (epithelial)
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Cellular systems studied:
cell lines
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Species studied:
human
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Enzymes shown to modify site in vitro:
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Upstream Regulation
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Potential in vivo enzymes for site:
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|
Type
|
Enzyme
|
Evidence
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Notes
|
|
PHOSPHATASE
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PPP1CA (human)
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pharmacological inhibitor of upstream enzyme
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|
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Treatments, proteins and their effect on site modification:
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|
Treatments
|
Referenced Treatments
|
Manipulated Protein
|
Referenced Protein
|
Effect
|
Notes
|
|
okadaic acid
|
|
|
|
increase
|
|
|
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Downstream Regulation
|
|
Effect of modification (function):
enzymatic activity, inhibited
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|
Modification regulates interactions with:
|
|
Interacting molecule
|
Interacting domains
|
Effect
|
Consequences (function)
|
Consequences (process)
|
Detection assays
|
|
CCNT1 (human)
|
|
Induces
|
|
|
co-immunoprecipitation
|
|
HEXIM1 (human)
|
|
Disrupts
|
|
|
co-immunoprecipitation
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|
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Comments:
CDK9 S175A mutant activates HIV-1 transcription
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