http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002529101-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-605
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P21-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-605
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-02
filingDate 1999-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2002-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002529101-A
titleOfInvention Enzymatic amidation of peptides
abstract (57) SUMMARY The present invention relates to a method for producing a polypeptide having a C-terminal α-carboxamide group. This is particularly the case for selected substrate polypeptides in which cleavage of the substrate polypeptide results in the formation of a polypeptide product having a C-terminal arginine residue with a C-terminal α-carboxamide group (C-terminal “Arg-NH 2 ”). For enzymatic modification of The method comprises the steps of contacting a water-based solution comprising (i) an ammonia reagent and (ii) a substrate polypeptide with (iii) clostripain.
priorityDate 1998-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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