Proteomics

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Jin_Context_dependent_interactions_between_HSP90_and_kinase_clientele


ABSTRACT: This submission consists of the mass spectrometry raw files for the manuscript by Jin et al. (Mutational analysis of GSK3B protein kinase together with kinome-wide binding and stability studies suggest context-dependent recognition of kinases by the chaperone HSP90). This submission contains files for the data presented as supplementary tables 2 and 3 acquired on an Orbitrap Velos.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

SUBMITTER: Karen Colwill 

PROVIDER: MSV000079445 | MassIVE | Wed Jan 06 07:25:00 GMT 2016

REPOSITORIES: MassIVE

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Publications

Mutational Analysis of Glycogen Synthase Kinase 3β Protein Kinase Together with Kinome-Wide Binding and Stability Studies Suggests Context-Dependent Recognition of Kinases by the Chaperone Heat Shock Protein 90.

Jin Jing J   Tian Ruijun R   Pasculescu Adrian A   Dai Anna Yue AY   Williton Kelly K   Taylor Lorne L   Savitski Mikhail M MM   Bantscheff Marcus M   Woodgett James R JR   Pawson Tony T   Colwill Karen K  

Molecular and cellular biology 20160111 6


The heat shock protein 90 (HSP90) and cell division cycle 37 (CDC37) chaperones are key regulators of protein kinase folding and maturation. Recent evidence suggests that thermodynamic properties of kinases, rather than primary sequences, are recognized by the chaperones. In concordance, we observed a striking difference in HSP90 binding between wild-type (WT) and kinase-dead (KD) glycogen synthase kinase 3β (GSK3β) forms. Using model cell lines stably expressing these two GSK3β forms, we observ  ...[more]

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