Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.7.11.2 (
PDK1
)
2,238
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Human nucleophosmin/
B23
is a phosphoprotein involved in ribosome biogenesis, centrosome duplication, cancer, and apoptosis. Its function, localization, and mobility within cells, are highly regulated by phosphorylation events. Up to 21 phosphosites of
B23
have been experimentally verified even though the corresponding kinase is known only for seven of them. In this work, we predict the phosphorylation sites in human
B23
using six kinase-specific servers (KinasePhos 2.0, PredPhospho, NetPhosK 1.0, PKC Scan, pkaPS, and MetaPredPS) plus DISPHOS 1.3, which is not kinase specific. The results were integrated with information regarding 3D structure and residue conservation of
B23
, as well as cellular localizations, cellular processes, signaling pathways and protein-protein interaction networks involving both
B23
and each predicted kinase. Thus, all 40 potential phosphosites of
B23
were predicted with significant score (>0.50) as substrates of at least one of 38 kinases. Thirteen of these residues are newly proposed showing high susceptibility of phosphorylation considering their solvent accessibility. Our results also suggest that the enzymes CDKs, PKC, CK2, PLK1, and PKA could phosphorylate
B23
at higher number of sites than those previously reported. Furthermore,
PDK
, GSK3, ATM, MAPK, PKB, and CHK1 could mediate multisite phosphorylation of
B23
, although they have not been verified as kinases for this protein. Finally, we suggest that
B23
phosphorylation is related to cellular processes such as apoptosis, cell survival, cell proliferation, and response to DNA damage stimulus, in which these kinases are involved. These predictions could contribute to a better understanding, as well as addressing further experimental studies, of
B23
phosphorylation.
...
PMID:In silico studies of potential phosphoresidues in the human nucleophosmin/B23: its kinases and related biological processes. 2257 54