. Author manuscript; available in PMC: 2019 Aug 2.

Published in final edited form as: Nat Chem. 2018 Mar 19;10(5):496–505. doi: 10.1038/s41557-018-0005-z

Table 1.

A summary of the ELPs, FAMEs, and control PAs used in this study.

	Identifier	N-terminal Modification	Sequence
	Identifier	N-terminal Modification	NMT Recognition sequences ^a)	ELP

	B₁-ELP	N/A	GAGASRGGSGGS
ELPs	B₂-ELP	N/A	GAGAGAYRGGSGGSGGS
	B₃-elp	N/A	GLSLSRGGSGGS	(GVGVP)₄₀GY
	M-B₁-ELP	Myristoyl	GAGASRGGSGGS	(GVGVP)₄₀GY
FAMEs	M-B₂-ELP	Myristoyl	GAGAGAYRGGSGGSGGS
	M-B₃-ELP	Myristoyl	GLSLSRGGSGGS

	M-B₁	Myristoyl	GAGASR
	M-B₂	Myristoyl	GAGAGAYR	N/A
Controls	M-B₃	Myristoyl	GLSLSR
	ELP	N/A	N/A	(GVGVP)₄₀GY
	M-ELP	Myristoyl	N/A	(GVGVP)₄₀GY

^a)

Amino acid abbreviations: Gly, G; Ala, A; Ser, S; Arg, R; Tyr, Y; Leu, L, Val, V and Pro, P. De novo designed recognition sequences contain a β-sheet forming domain (bold), trypsin cleavage site (Arg, underlined), and a flexible linker (italics).