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. 2021 May 27;11:11211. doi: 10.1038/s41598-021-90613-9

Table 2.

Possible tryptic peptides of homicorcin and its variant and their presence in MS analysis.

Peptide fragment Domain Tryptic peptide m/z Presence in MS
Homicorcin/
homicorcin 1
A/A’ N-terminal S(de)LGTAIK/S(hpo)LGTAIK 653.4/656.8  + 
B N-terminal AT(de)K 301.2
C N-terminal NACPK 532.2
B + C N-terminal AT(de)KNACPK 814.4  + 
D Hinge VT(de)R 357.2  + 
B + C + D N-terminal + Hinge AT(de)KNACPKVT(de)R 1153.5  + 
E C-terminal LVT(de)VS(de)CQK 841.5
F C-terminal S(de)DCQ 434.1
D + E Hinge + C-terminal VT(de)RLVT(de)VS(de)CQK 1179.7
E + F C-terminal LVT(de)VS(de)CQKS(de)DCQ 1256.6  + 
D + E + F Hinge + C-terminal VT(de)RLVT(de)VS(de)CQKS(de)DCQ 1594.8

A’ denotes fragment A of homicorcin 1 where dehydrated first Ser residue was modified to 2-hydroxypropionate (Hpo). Domain name represents the fragment position in the core peptide. Bold and underlined ‘S(de)’ or ‘T(de)’ residues are predicted to be dehydrated and ‘C’ are predicted to form thio-ether linkage with dehydrated S/T residues. . ( +) and (−) represents the presence or absence respectively of the fragment in MS analysis.