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 | UniProt | Comment | Textmining |
---|---|---|---|
Pseudomonas fragi | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
commercial preparation | recombinant enzyme | Pseudomonas fragi | - |
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 | ? | - |
? |
Synonyms | Comment | Organism |
---|---|---|
AspN | - |
Pseudomonas fragi |
endoproteinase AspN | - |
Pseudomonas fragi |