Curated Information
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Curated Information Page
PubMed Id: 16495336 
This page summarizes selected information from the article 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.
Nichols RJ, Wiebe MS, Traktman P (2006) The vaccinia-related kinases phosphorylate the N' terminus of BAF, regulating its interaction with DNA and its retention in the nucleus. Mol Biol Cell 17, 2451-64 16495336
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.
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T2-p - BAF (human) ▲
Orthologous residues
BAF (human): T2‑p, BAF (mouse): T2‑p, BAF (rat): T2‑p
Characterization
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE VRK1 (human)
KINASE VRK2 (human)
Upstream Regulation
 Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE VRK1 (human) transfection of inactive enzyme, transfection of wild-type enzyme
Downstream Regulation
 Effect of modification (function):  intracellular localization, molecular association, regulation
 Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
DNA Disrupts

T3-p - BAF (human) ▲
Orthologous residues
BAF (human): T3‑p, BAF (mouse): T3‑p, BAF (rat): T3‑p
Characterization
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE VRK2 (human)
KINASE VRK1 (human)
Upstream Regulation
 Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE VRK1 (human) transfection of inactive enzyme, transfection of wild-type enzyme
Downstream Regulation
 Effect of modification (function):  intracellular localization, molecular association, regulation
 Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
DNA Disrupts

S4-p - BAF (human) ▲
Orthologous residues
BAF (human): S4‑p, BAF (mouse): S4‑p, BAF (rat): S4‑p
Characterization
 Enzymes shown to modify site in vitro: 
Type Enzyme
KINASE VRK1 (human)
KINASE VRK2 (human)
Upstream Regulation
 Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE VRK1 (human) transfection of inactive enzyme, transfection of wild-type enzyme
Downstream Regulation
 Effect of modification (function):  intracellular localization, molecular association, regulation
 Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
DNA Disrupts


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