Protein Disulphide Linkage Modeler
1. Define the protein sequence for the model.
Protein name
Sequence
2. Describe the chemistry used to generate sequence fragments.
Enzyme
Trypsin
Missed cleaves
0
1
2
3
4
5
6
Complete
modifications
Unmodified
4-vinyl-pyridine (Cys)
Acrylamide (Cys)
Iodoacetamide (Cys)
Iodoacetic acid (Cys)
Performic acid (Cys+O3)
Performic acid (Met+O2)
Performic acid (Met+O)
Partial
modifications
Unmodified
4-vinyl-pyridine (Cys)
Acrylamide (Cys)
Iodoacetamide (Cys)
Iodoacetic acid (Cys)
Nitration (Y)
Oxidation (M)
Performic acid (Cys+O3)
Performic acid (Met+O2)
Performic acid (Met+O)
Phosphorylation (S,T,Y)
Phosphorylation (S,T)
Phosphorylation (Y)
3. Enter the mass spectrum results for the model.
Average
masses
Monoisotopic
masses
Tolerance ±
Tolerance ±
Tolerance units
Da
%
ppm
Mass type
M
MH+
4. Filter the results for the model.
Max Free AAs
0
1
2
3
4
Max Fragments Linked
2
3
4
5
6
Max Link Attachments
1
2
3
4
5
6
5. Finally, to generate the models that fit this data set,
Notes: To fill in this form with some example data,
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