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Literature summary for 3.4.24.33 extracted from

  • Sonomura, K.; Kuyama, H.; Matsuo, E.; Tsunasawa, S.; Futaki, S.; Nishimura, O.
    Selective isolation of N-blocked peptide by combining AspN digestion, transamination, and tosylhydrazine glass treatment (2011), Anal. Biochem., 410, 214-223.
    View publication on PubMed

Application

Application Comment Organism
molecular biology many eukaryotic proteins are blocked at the alpha-amino group of their N-terminal with various modifications, thereby making it difficult to determine their N-terminal sequence by protein sequencer, development of a method for selectively isolating the blocked N-terminal peptide from the peptide mixture generated by endoproteinase AspN digestion of N-blocked protein by removal of all peptides other than the N-terminal one (non-N-terminal peptides) through their carbonyl group introduced by a chemical transamination reaction Pseudomonas fragi

Organism

Organism UniProt Comment Textmining
Pseudomonas fragi
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Source Tissue

Source Tissue Comment Organism Textmining
commercial preparation recombinant enzyme Pseudomonas fragi
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information high substrate specificity of AspN, that ensures that all of the non-N-terminal peptides having aspartic acid or glutamic acid at their N-termini can be converted. An artificially targeted N-blocked protein is digested with AspN, method overview. The proposed method is applicable to proteins, whether N blocked or N free Pseudomonas fragi ?
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Synonyms

Synonyms Comment Organism
AspN
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Pseudomonas fragi
endoproteinase AspN
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Pseudomonas fragi