LOCUS BAA02632.1 392 aa PRT HUM 12-SEP-2008 DEFINITION Homo sapiens alanine:glyoxylate aminotransferase protein. ACCESSION D13368-1 PROTEIN_ID BAA02632.1 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 1325) AUTHORS Minatogawa,Y. TITLE Direct Submission JOURNAL Submitted (05-OCT-1992) to the DDBJ/EMBL/GenBank databases. Contact:Yohsuke Minatogawa Wakayama Medical College, Department of Biochemistry; 9-27, Wakayama, Wakayama 640, Japan REFERENCE 2 AUTHORS Takada,Y., Kaneko,N., Esumi,H., Purdue,P.E. and Danpure,C.J. TITLE Human peroxisomal L-alanine:glyoxylate aminotransferase:Evolutionary loss of a mitochondrial targeting signal by point mutation JOURNAL Biochem. J. 268, 517-520 (1990) REFERENCE 3 AUTHORS Minatogawa,Y., Tone,S., Allsop,J., Purdue,E.P., Takada,Y., Danpure,C.J. and Kido,R. TITLE A serine-to-phenylalanine substitution leads to loss of alanine: glyoxylate aminotransferase catalytic activity and immunoreactivity in a patient with primary hyperoxaluria type 1 JOURNAL Hum. Mol. Genet. 1, 643-644 (1992) COMMENT FEATURES Qualifiers source /chromosome="2" /clone="P2-3, P2-7" /db_xref="H-InvDB:HIT000100497" /db_xref="taxon:9606" /isolate="Patient 2" /map="2q36-q37" /mol_type="mRNA" /note="patient of primary hyperoxaluria type 1" /organism="Homo sapiens" /tissue_type="liver" protein /EC_number="2.6.1.44" /gene="AGXT" BEGIN 1 MASHKLLVTP PKALLKPLSI PNQLLLGPGP SNLPPRIMAA GGLQMIGSMS KDMYQIMDEI 61 KEGIQYVFQT RNPLTLVISG SGHCALEAAL VNVLEPGDSF LVGANGIWGQ RAVDIGERIG 121 ARVHPMTKDP GGHYTLQEVE EGLAQHKPVL LFLTHGESST GVLQPLDGFG ELCHRYKCLL 181 LVDSVAFLGG TPLYMDRQGI DILYSGSQKA LNAPPGTSLI SFSDKAKKKM YSRKTKPFSF 241 YLDIKWLANF WGCDDQPRMY HHTIPVISLY SLRESLALIA EQGLENSWRQ HREAAAYLHG 301 RLQALGLQLF VKDPALRLPT VTTVAVPAGY DWRDIVSYVI DHFDIEIMGG LGPSTGKVLR 361 IGLLGCNATR ENVDRVTEAL RAALQHCPKK KL //