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. 2013 Sep 20;8(9):e68014. doi: 10.1371/journal.pone.0068014

Table 1. N-terminal sequences of proDer p 3 zymogens obtained after purification at 4°C.

Proteins Expected and observed N-terminal sequences Approximate (%)
proDer p 3 NPILPASPQAT IVGGEKALAG
4°C EFNPILPASPQATIVGGEKALAG 100
P2A proDer p 3 NAILPASPQAT IVGGEKALAG
4°C EFNAILPASPQATIVGGEKALAG 100
P5A proDer p 3 NPILAASPQAT IVGGEKALAG
4°C EFNPILAASPQATIVGGEKALAG 100
P8A proDer p 3 NPILPASAQAT IVGGEKALAG
4°C EFNPILPASAQATIVGGEKALAG 100
P-A proDer p 3 NAILAASAQAT IVGGEKALAG
4°C EFNAILAASAQATIVGGEKALAG 8
ILAASAQATIVGGEKALAG 5
ASAQATIVGGEKALAG 9
SAQATIVGGEKALAG 42
AQATIVGGEKALAG 16
ATIVGGEKALAG 14
ALAGE 6
Δ1–2 proDer p 3 ILPASPQAT IVGGEKALAG
4°C EFILPASPQATIVGGEKALAG 88
SPQATIVGGEKALAG 3
Not identified 9
Δ1–5 proDer p 3 ASPQAT IVGGEKALAG
4°C EFASPQATIVGGEKALAG 88
ATIVGGEKALAG 8
Not identified 4
Δ1–8 proDer p 3 QAT IVGGEKALAG
4°C EFQATIVGGEKALAG 24
EAEFQATIVGGEKALAG 74
Not identified 2
Δ1–11 proDer p 3 IVGGEKALAG…
4°C EAEFIVGGEKALAG 94
EAEAEFIVGGEKALAG 6

All proteins contain the N9Q mutation, which abolishes N-glycosylation of the propeptide. The mature Der p 3 sequence is shown in italics. The EF N-terminal extension resulted from cloning.