Synthetic segments of the mammalian beta AR are preferentially recognized by cAMP-dependent protein kinase and protein kinase C (Q69806569)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2820394%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

title

Synthetic segments of the mammalian beta AR are preferentially recognized by cAMP-dependent protein kinase and protein kinase C (English)

1 reference

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5 October 2019

author name string

A D Blake

1

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5 October 2019

R A Mumford

2

1 reference

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5 October 2019

H V Strout

3

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5 October 2019

E E Slater

4

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5 October 2019

C D Strader

5

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5 October 2019

language of work or name

English

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publication date

1 August 1987

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Biochemical and Biophysical Research Communications

5 October 2019

published in

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5 October 2019

volume

147

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5 October 2019

issue

1

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5 October 2019

page(s)

168-173

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Molecular mechanisms of receptor desensitization using the beta-adrenergic receptor-coupled adenylate cyclase system as a model

5 October 2019

cites work

1 reference

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Phorbol diester treatment promotes enhanced adenylate cyclase activity in frog erythrocytes

7 January 2021

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Cloning of the gene and cDNA for mammalian beta-adrenergic receptor and homology with rhodopsin

7 January 2021

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Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide

7 January 2021

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Phosphorylation by protein kinase C of a synthetic heptapeptide bearing a lysine residue on the C terminal side of serine

7 January 2021

1 reference

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Substrate specificity of protein kinase C. Use of synthetic peptides corresponding to physiological sites as probes for substrate recognition requirements

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2887%2980102-X

Synthetic myelin basic protein peptide analogs are specific inhibitors of phospholipid/calcium-dependent protein kinase (protein kinase C).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2887%2980102-X

Phosphorylation-Dephosphorylation of Enzymes

7 January 2021

1 reference

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10.1016/S0006-291X(87)80102-X

7 January 2021

Identifiers

DOI

1 reference

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5 October 2019

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