http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H1045796-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_02ff914937eb6ceaee5ca69cc56cbfa7
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-19
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-04
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filingDate 1996-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_565d38e0f151618a607b2a095193e76d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c46972dbee1870eac37eb88b1c7fa078
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_05f6142d006675b839683c001ca7f9e2
publicationDate 1998-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H1045796-A
titleOfInvention Method for site-specific fragmentation of proteins
abstract (57) [Summary] The object of the present invention is to provide an efficient method for site-specific fragmentation of a protein. SOLUTION: A lysine-cysteine residue is introduced into a peptide, and then cysteine is cyanated. Then When the peptide is treated with a weak alkali, the ε-amino group of lysine attacks the carbonyl carbon on the peptide bond by lysine and cyanocysteine as a nucleophilic group, and Cleavage of the peptide bond of cyanocysteine was efficiently triggered.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007091907-A1
priorityDate 1996-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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