Synthetic mammalian sulphamidase and genetic sequences encoding same
a technology of mammalian sulphamidase and genetic sequences, applied in the direction of sugar derivatives, biochemistry apparatus and processes, enzymes, etc., can solve the problems of difficult purification of target molecules, particularly in research and development, and many difficulties for practitioners
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example 2
Characterisation of Sulphamidase
[0064] Results presented in FIG. 1 show a subunit of about M.sub.r 56,000 from sulphamidase purified from human liver, kidney and placenta The native M.sub.r is about 100,000 to 120,000.
example 3
N-Terminal Amino Acid Sequence Determination
[0065] The N-terminal amino acid sequence was determined using the methods of Clements et al (1989) and Wilson et al (1990).
[0066] The amino acid sequence is shown in Table 2.
example 4
Cloning of Sulphamidase cDNA
[0067] The N-terminal amino acid sequence (Example 3) was used to generate oligonucleotides and primers to screen a human kidney cDNA library. An approximately 2.7 kbp cDNA clone was then isolated encoding the entire sequence of human sulphamidase. The nucleotide sequence (SEQ ID NO:1) and corresponding amino acid sequence (SEQ ID NO:2) are shown in FIG. 2.
[0068] The amino acid sequence is shown in single letter code above the cDNA sequence. Nucleotide and amino acid numbers are in the right margin. The probable site of signal peptide peptidase cleavage between amino acids 20 and 21 is shown by an arrow. Amino acids colinear with the amino-terminal peptide data is underlined. The five potential N-glycosylation sites are asterisked above the peptide sequence. The open reading frame is 1506 nucleotides long and encodes a 502 amino acid protein. The predicted molecular mass of the mature protein (minus the 20 amino acid signal peptide) is about 54,679 kilo d...
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