Summary of the bioactive peptides' primary structures and antimicrobial activities showed in Fig. 1. NA stands for non-available.

Group	Peptide name	Sequence and disulfide structure	MIC (μM)	Ref.
α-Defensin	CRP4		<5	38 and 39
β-Defensins			N.A. oxidized	49
			2.3–23	50
			0.7–1.2	51
θ-Defensin	RTD-1		0.5–5	61 and 62
Cathelicidins	PG-1		0.03–0.4	72 and 76
	LL-37		1–10	88
Cyclotides	Kalata B1		0.29–14	122
	MCo-PG2		0.8–12.5	77
SFTI-I derived	RV3		0.6–4	134 and 135
β-Hairpin	Gomesin		0.2–6	136
	Thanatin		0.5–2	142 and 143