http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1670940-B1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10
filingDate 2004-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9f8f2f503e92ee370b5699a37a7485d5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1700296e8c52914a1601b13b9ac5c410
publicationDate 2010-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1670940-B1
titleOfInvention Method for identification of suitable fragmentation sites in a reporter protein
abstract The invention concerns a combinatorial method for the generation of new split-protein sensors, and its application towards the (β/α)8-barrel enzyme N-(5′-phosphoribosyl)-anthranilate isomerase Trp1p from Saccharomyces cerevisiae is demonstrated. The generated split-Trp protein sensors allow for the detection of protein-protein interactions in the cytosol as well as the membrane by enabling trp1 cells to grow on medium lacking tryptophan. This powerful selection thus complements the repertoire of the currently used split-protein sensors and provides a new tool for high-throughput interaction screening.
priorityDate 2003-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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