LOCUS       AAB59569.1               428 aa    PRT              HUM 30-SEP-1995
DEFINITION  Homo sapiens MSH2 protein.
ACCESSION   L47577-1
PROTEIN_ID  AAB59569.1
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 2919)
  AUTHORS   Wijnen,J., Vasen,H., Khan,P.M., Menko,F.H., van der Klift,H., van
            Leeuwen,C., van den Broek,M., van Leeuwen-Cornelisse,I.,
            Nagengast,F., Meijers-Heijboer,A., Lindhout,D., Griffioen,G.,
            Cats,A., Kleibeuker,J., Varesco,L., Bertario,L., Bisgaard,M.L.,
            Mohr,J. and Fodde,R.
  TITLE     Seven new mutations in hMSH2, an HNPCC gene, identified by
            denaturing gradient-gel electrophoresis
  JOURNAL   Am. J. Hum. Genet. 56 (5), 1060-1066 (1995)
   PUBMED   7726159
COMMENT     Original source text: Homo sapiens cDNA to mRNA.
FEATURES             Qualifiers
     source          /db_xref="H-InvDB:HIT000193923"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /map="7p21"
     protein         /gene="MSH2"
                     /note="mutation causes premature stop"
BEGIN
        1 MAVQPKETLQ LESAAEVGFV RFFQGMPEKP TTTVRLFDRG DFYTAHGEDA LLAAREVFKT
       61 QGVIKYMGPA GAKNLQSVVL SKMNFESFVK DLLLVRQYRV EVYKNRAGNK ASKENDWYLA
      121 YKASPGNLSQ FEDILFGNND MSASIGVVGV KMSAVDGQRQ VGVGYVDSIQ RKLGLCEFPD
      181 NDQFSNLEAL LIQIGPKECV LPGGETAGDM GKLRQIIQRG GILITERKKA DFSTKDIYQD
      241 LNRLLKGKKG EQMNSAVLPE MENQVAVSSL SAVIKFLELL SDDSNFGQFE LTTFDFSQYM
      301 KLDIAAVRAL NLFQGSVEDT TGSQSLAALL NKCKTPQGQR LVNQWIKQPL MDKNRIEERL
      361 NLVEAFVEDA ELRQTLQEDL LRRFPDLNRL AKKFQRQAAN LQDCYRLYQG INQLPNVIQA
      421 LEKHEGKH
//