http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0889899-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-30
filingDate 1997-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3de2f075944736cce56f7391e4c9004f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae4f6c953ba4cf8fb9fb41c042c91e2b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a72b563b2691c3f0cabe16b72823191
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14a7060c17a77d5e6c81d001556e89e5
publicationDate 1999-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0889899-A1
titleOfInvention Mycoplasma arthritidis superantigen
abstract The gene encoding the superantigen Mycoplasma arthritidis T-cell mitogen (MAM) was molecularly cloned. The mam gene was modified by site-directed mutagenesis to change UGA codons, which in mycoplasmas are read as tryptophan codons instead of universal stop codons, to UGG codons such that the gene could be expressed in standard expression systems. Recombinant MAM, including extra amino acid residues at the - and C-termini, were expressed and discovered to be biologically active. Certain amino acid substitutions in active regions of the protein also yield biologically active MAM proteins. A method of diagnosing rheumatoid arthritis using recombinant MAM protein in an ELISA assay is disclosed.
priorityDate 1996-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 427.