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Proteintech
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Immunogen sequence: MAGAEWKSL EECLEKHLPL PDLQEVKRVL YGKELRKLDL PREAFEAASR EDFELQGYAF EAAEEQLRRP RIVHVGLVQN RIPLPANAPV AEQVSALHRR IKAIVEVAAM CGVNIICFQE AWTMPFAFCT REKLPWTEFA ESAEDGPTTR FCQKLAKNHD MVVVSPILER DSEHGDVLWN TAVVISNSGA VLGKTRKNHI PRVGDFNEST YYMEGNLGHP VFQTQFGRIA VNICYGRHHP LNWLMYSING AEIIFNPSAT IGALSESLWP IEARNAAIAN HCFTCAINRV GTEHFPNEFT SGDGKKAHQD FGYFYGSSYV AAPDSSRTPG LSRSRDGLLV AKLDLNLCQQ VNDVWNFKMT GRYEMYAREL AEAVKSNYSP TIVKE (1-384 aa encoded by BC131703)
UPB1 is a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activity. This gene encodes a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activity.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Beta-alanine synthase; Beta-ureidopropionase; BUP-1; N-carbamoyl-beta-alanine amidohydrolase; ureidopropionase, beta
基因别名: AI195023; BUP1; UPB1
UniProt ID: (Human) Q9UBR1, (Mouse) Q8VC97
Entrez Gene ID: (Human) 51733, (Mouse) 103149