Skip to main content
. Author manuscript; available in PMC: 2020 Jan 4.
Published in final edited form as: J Proteome Res. 2018 Oct 31;18(1):349–358. doi: 10.1021/acs.jproteome.8b00651

Table 1.

Common Sequence Similarity Types and Their Frequencies in Nonspliced and Cis-Spliced Searches

Observed Peptide Similar Sequencea Nonspliced Frequencyb Cis-Spliced Frequencyb
Permutation CQMMQNPRACLEMS QCMMQNPRAGLEMS 1.42E-3 0.660
Replacement CQMMQNPRACLEMS CQMMQNPRAGLDMT 2.57E-4 0.384
Insertion CQMMQNPRAGLEMS CQMMQGGPRAGLEMS 2.56E-5 0.106
Deletion CQMMQNPRAGLEMS CQMMQN PRQLEMS Ί.76Ε−5 0.054
Substitution CQMMQNPRAGLEMS CQMMQNPRAGLEME 1.69E-4 0.265
         Acetyl
a

These sequences have identical precursor masses and similar fragmentation patterns, making the correct sequence diffcult to distinguish.

b

Frequencies are the average number of similar sequences per theoretical peptide. This was calculated for 9-mer, nonspliced peptides from the human.xml database. The computational power required for this calculation limited the similarity comparisons to peptides generated from the same protein. The database-wide frequencies are thus expected to be much higher.