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. 2005 Sep 26;391(Pt 1):135–142. doi: 10.1042/BJ20050640

Table 1. Partial-proteolysis fragments of (His)8-rP[I-V].

The protein bands (partial-proteolysis fragments) labelled alphabetically in Figure 3(A) were subjected to N-terminal sequencing, the results of which were used to decide their N-terminal positions. The molecular masses were calculated from the migration on SDS/PAGE, which was performed several times to yield errors less than 0.5 kDa. These data were used for prediction of the C-terminal positions. When the fragments seemed to be produced by cleavage at their N-terminal ends only, the ‘position of C-terminal aa’ is indicated as 520.

Fragment Protease N-terminal sequence Position of N-teminal aa Predicted molecular mass (kDa) Predicted position of C-teminal aa
a Trypsin TTEGL 60 52 520
b Trypsin LSSYP 69 50 515
c Trypsin RANKK 85 47 501 or 502 or 503
d Trypsin RAANS 92 46 501 or 502 or 503
e Glu-C VASTK 35 55 520
f Glu-C VASTK 35 52 495 or 498
g Glu-C GLPNM 63 49 484
h Glu-C VASTK 35 47 451 or 454
i Glu-C GLPNM 63 44 451 or 454
j Glu-C GLPNM 63 43 451 or 454
k Lys-C NINSP 50 53 520
l Lys-C LSSYP 69 50 520
m Lys-C NINSP 50 46 464
n Lys-C LSSYP 69 43 455
o Lys-C GRRAA 90 41 455