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. 2001 Oct;75(19):9458–9469. doi: 10.1128/JVI.75.19.9458-9469.2001

TABLE 3.

HIV-1 and FIV PR cleavage of FIV PR selected phage-derived peptidesa

Peptide Peptide sequencec HIV-1 PR cleavageb FIV PR cleavageb
R3 20   KGSGVF↓AVTQLVPK ++ +++
R2 13   KGSGIY↓TVQSLVPK ++ +++
R1 8  KGSGLTM↓VTQLVPK +++
R3 21   KGSGVY↓QL d SALVPK + ++, ++d
R2 20 KGSGALTN↓AVLVPK +++
R3 14 KGSGAMVN↓QALVPK +++
R3 25   KGSGTW↓MVHSLVPK +++
R3 30 KGSGGRIN↓VALVPK + +++
a

All peptide sequences listed above were derived from phage selected as described in Materials and Methods. A 500 μM concentration of each peptide was digested with 312 nM FIV PR or 160 nM HIV-1 PR for 2 h at pH 6.7 in 0.2 M NaCl. 

b

−, peptide cleavage not detected by HPLC; +, peptide cleavage detected at <5%; ++, peptide cleavage detected at between 10 and 90%; +++, 100% cleavage of the peptide. 

c

Cleavage site for both HIV-1 PR and FIV PR is denoted by an arrow as determined by mass spectrometry of the cleaved fragments. 

d

FIV PR cleaved peptide R3 21 at two sites, the second marked by this footnote reference. None of the starting peptide remained after cleavage, and each product was identified at >20% of the original peptide concentration.