Development of highly selective SH3 binding peptides for Crk and CRKL which disrupt Crk-complexes with DOCK180, SoS and C3G

Oncogene

Volumn 16, Issue 15, 1998, Pages 1903-1912

  Posern, Guido ^a   Zheng, Jie ^b   Knudsen, Beatrice S ^b   Kardinal, Christian ^a   Müller, Kerstin B ^a   Voss, Jan ^a   Shishido, Tomoyuki ^b   Cowburn, David ^b   Cheng, Genhong ^c,h   Wang, Baolin ^d,e   Kruh, Gary D ^e   Burrell, Sarah K ^f   Jacobson, Christina A ^f   Lenz, Douglas M ^f   Zamborelli, Thomas J ^f   Adermann, Knut ^g   Hanafusa, Hidesaburo ^b   Feller, Stephan M ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b ROCKEFELLER UNIVERSITY   (United States)

^c MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

^e FOX CHASE CANCER CENTER   (United States)

^f AMGEN INC   (United States)

^g IPF PHARMACEUTICALS GMBH   (Germany)

^h UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Adapters; Crk; CRKL; Peptide; SH3

Indexed keywords

ADAPTOR PROTEIN; CELL PROTEIN; HYBRID PROTEIN; MUTANT PROTEIN; PEPTIDE; SULFUR 35;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; COMPLEX FORMATION; CONTROLLED STUDY; ISOTOPE LABELING; NONHUMAN; ONCOGENE SRC; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; SEQUENCE HOMOLOGY; STRUCTURE ACTIVITY RELATION;

ANIMALIA;

EID: 7144263722     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1201714     Document Type: Article

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