| Literature DB >> 27151216 |
Yuya Fujiwara1, Yoshinori Kawaguchi1, Tomohito Fujimoto2, Naoki Kanayama1, Masaki Magari1, Hiroshi Tokumitsu3.
Abstract
Ca(2+)/calmodulin-dependent protein kinase kinase β (CaMKKβ) is a known activating kinase for AMP-activated protein kinase (AMPK). In vitro, CaMKKβ phosphorylates Thr(172) in the AMPKα subunit more efficiently than CaMKKα, with a lower Km (∼2 μm) for AMPK, whereas the CaMKIα phosphorylation efficiencies by both CaMKKs are indistinguishable. Here we found that subdomain VIII of CaMKK is involved in the discrimination of AMPK as a native substrate by measuring the activities of various CaMKKα/CaMKKβ chimera mutants. Site-directed mutagenesis analysis revealed that Leu(358) in CaMKKβ/Ile(322) in CaMKKα confer, at least in part, a distinct recognition of AMPK but not of CaMKIα.Entities:
Keywords: AMP-activated kinase (AMPK); Ca2+/calmodulin-dependent protein kinase (CaMK); CaMKI; CaMKK; calmodulin (CaM); phosphorylation; substrate recognition; substrate specificity
Mesh:
Substances:
Year: 2016 PMID: 27151216 PMCID: PMC4919462 DOI: 10.1074/jbc.M116.727867
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157