(Q46866542)

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Structural basis for the binding of high affinity phosphopeptides to Stat3.

scientific article published in January 2008

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

title

Structural basis for the binding of high affinity phosphopeptides to Stat3. (English)

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stated in

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

author name string

John S McMurray

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1

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

publication date

1 January 2008

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

published in

Biopolymers

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

volume

90

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26 December 2017

http://europepmc.org/abstract/MED/18058821

issue

1

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

page(s)

69-79

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

cites work

Stat proteins and oncogenesis

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FBIP.20901

retrieved

21 January 2018

Antagonists of the Src homology 2 (SH2) domains of Grb2, Src, Lck and ZAP-70.

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FBIP.20901

retrieved

21 January 2018

Unique structural determinants for Stat3 recruitment and activation by the granulocyte colony-stimulating factor receptor at phosphotyrosine ligands 704 and 744.

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FBIP.20901

retrieved

21 January 2018

Identifiers

DOI

10.1002/BIP.20901

1 reference

stated in

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

PubMed ID

18058821

1 reference

stated in

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/18058821

ResearchGate publication ID

5789034

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(Q46866542)

Structural basis for the binding of high affinity phosphopeptides to Stat3.

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