These data have been prepared by Mike Adams, Rothamsted Research, using all sequences available on June 30th 2013. The pages were previously hosted on the Rothamsted Research web site but have now been moved here to provide a single site for information on, and analysis of, plant virus sequences. This information is based on published data and our own analyses as reported in the paper: Adams, Antoniw & Beaudoin (2005). Overview and analysis of the polyprotein cleavage sites in the family Potyviridae. Molecular Plant Pathology 6, 471-487.
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The ssRNA genome of members of the family Potyviridae encodes a polyprotein that is subsequently processed by virus-encoded proteases to generate functional proteins. The cleavage sites show considerable sequence conservation but with some variations that have phylogenetic significance. The genome organisation of a typical member of the family is shown in Figure 1 which indicates the 10 mature proteins and the nine cleavage sites (arrowed). In some members of the genus Ipomovirus, there appear to be two copies of the P1 protein (P1a and P1b) and the HC-Pro is absent.
Figure 1. Potyvirus genome map
Figure 2. Bymovirus genome map
The following tables provide summaries of the polyprotein cleavage sites within the family. Usually 4 amino acids are shown before the cleavage site and one after, as this includes most of the sequence conservation. In most cases these sequences are deduced from peptide alignments. In a few cases, the sites differ in position from those given in the sequence file header and so represent my estimates rather than those of the original authors. All the available sequences in the family Potyviridae available were used, whether complete or partial (see top of page for date of latest update). The accuracy of these data are only as good as the underlying sequence files and some of the apparently unusual cleavage sites (especially where only detected once) may arise from errors in sequencing.
Site | Nos of sequences | Nos of viruses |
AXHF/S | 2 | 1 |
FXWY/G | 2 | 1 |
IXEF/S | 20 | 3 |
IXFY/A | 17 | 3 |
IXFY/C | 1 | 1 |
IXFY/T | 1 | 1 |
IXHF/I | 1 | 1 |
IXHF/S | 168 | 5 |
IXHY/A | 140 | 7 |
IXHY/N | 1 | 1 |
IXHY/S | 307 | 25 |
IXHY/T | 9 | 3 |
IXLY/G | 1 | 1 |
IXLY/S | 17 | 2 |
IXMY/S | 2 | 1 |
IXQF/S | 19 | 4 |
IXQY/A | 1 | 1 |
IXQY/S | 5 | 3 |
IXYY/S | 3 | 2 |
KXSF/T | 1? | 1? |
LXFY/S | 3 | 1 |
LXFY/T | 26 | 1 |
LXHY/A | 3 | 1 |
LXHY/S | 15 | 3 |
LXHY/T | 1 | 1 |
LXLY/T | 2 | 1 |
LXQY/S | 1 | 1 |
LXWY/C | 1 | 1 |
LXWY/G | 12 | 1 |
LXWY/S | 1 | 1 |
LXYF/S | 1 | 1 |
LXYY/S | 2 | 1 |
MXEY/S | 2 | 1 |
MXFY/A | 1 | 1 |
MXFY/S | 1 | 1 |
MXHF/S | 14 | 7 |
MXHY/M | 1 | 1 |
MXHY/S | 28 | 143 |
MXQF/A | 1 | 1 |
MXQF/N | 1 | 1 |
MXQF/S | 292 | 7 |
MXQY/N | 25 | 1 |
MXQY/S | 30 | 7 |
TXHF/S | 1 | 1 |
TXHY/S | 18 | 6 |
VXFY/A | 1 | 1 |
VXFY/S | 1 | 1 |
YXHY/A | 1 | 1 |
YXHY/N | 2 | 1 |
VXHY/S | 68 | 9 |
YXQY/S | 1 | 1 |
Dipeptide summary | ||
F/A | 1 | 1 |
F/I | 1 | 1 |
F/N | 1 | 1 |
F/S | 515 | 29 |
F/T | 1? | 1? |
Y/A | 170 | 13 |
Y/C | 2 | 2 |
Y/G | 15 | 3 |
Y/M | 1 | 1 |
Y/N | 28 | 3 |
Y/S | 498 | 71 |
Y/T | 39 | 5 |
Site | Nos of sequences | Nos of viruses |
CXVG/G | 3 | 1 |
FXIG/G | 3 | 1 |
FXVG/G | 1 | 1 |
LXCG/G | 1 | 1 |
YXIG/G | 37 | 10 |
YXMG/G | 1 | 1 |
YXVG/A | 1 | 1 |
YXVG/G | 1037 | 98 |
YXVG/R | 1 | 1 |
Virus | Site | Nos of sequences |
Barley mild mosaic virus | YXVG/A | 11 |
Barley yellow mosaic virus | GXVG/S | 9 |
Oat mosaic virus | FXTG/N | 1 |
Wheat yellow mosaic virus | GXVG/S | 7 |
Click here for a summary of the most important sites by genus
P3/6K1 | 6K1/CI | CI/6K2 | 6K2/VPg | VPg/NIa-Pro | NIa-Pro/NIb | NIb/CP | ||||||||||||||
Seqs | Species | Seqs | Species | Seqs | Species | Seqs | Species | Seqs | Species | Seqs | Species | Seqs | Species | |||||||
E/A | 5 | 3 | 428 | 9 | 336 | 27 | 18* | 4 | ||||||||||||
E/G | 26 | 2 | 1 | 1 | 2 | 2 | 76 | 17 | 106 | 32 | 3 | 1 | ||||||||
E/H | 2 | 1 | 1 | 1 | ||||||||||||||||
E/I | 2 | 2 | ||||||||||||||||||
E/M | 2 | 2 | 1 | 1 | ||||||||||||||||
E/N | 1 | 1 | 1 | 1 | 11 | 4 | ||||||||||||||
E/Q | 1 | 1 | ||||||||||||||||||
E/R | 1 | 1 | 1 | 1 | ||||||||||||||||
E/S | 4 | 3 | 1 | 1 | 30 | 7 | 47 | 1 | 840 | 51 | 1 | 1 | 91 | 4 | ||||||
E/T | 1 | 1 | 2 | 1 | ||||||||||||||||
E/V | 2 | 1 | ||||||||||||||||||
G/A | 1 | 1 | ||||||||||||||||||
G/S | 2 | 1 | ||||||||||||||||||
H/A | 27 | 2 | 42 | 4 | 1 | 1 | 25 | 1 | 24 | 1 | 80 | 2 | ||||||||
H/G | 15 | 2 | 1 | 1 | 27 | 2 | 6 | 5 | 23 | 2 | 1 | 1 | ||||||||
H/N | 3 | 2 | ||||||||||||||||||
H/S | 2 | 2 | 2 | 2 | 4 | 3 | 3 | 3 | 8 | 4 | ||||||||||
H/V | 1 | 1 | ||||||||||||||||||
K/L | 1 | 1 | ||||||||||||||||||
K/W | 1 | 1 | ||||||||||||||||||
M/S | 1 | 1 | 1 | 1 | ||||||||||||||||
Q/A | 550 | 61 | 67 | 12 | 226 | 5 | 50 | 14 | 1 | 1 | 327 | 21 | 1717 | 81 | ||||||
Q/C | 14 | 2 | 33 | 2 | 1 | 1 | ||||||||||||||
Q/D | 9 | 4 | 8 | 1 | 7 | 4 | 2 | 1 | 9 | 2 | ||||||||||
Q/E | 1 | 1 | 1 | 1 | 2 | 2 | ||||||||||||||
Q/F | 1 | 1 | ||||||||||||||||||
Q/G | 56 | 11 | 43 | 7 | 59 | 12 | 722 | 78 | 3 | 1 | 135 | 30 | 228 | 29 | ||||||
Q/H | 2 | 2 | 1 | 1 | 6 | 5 | ||||||||||||||
Q/I | 1 | 1 | ||||||||||||||||||
Q/K | 14 | 9 | 2 | 2 | ||||||||||||||||
Q/L | 5 | 2 | 2 | 1 | ||||||||||||||||
Q/M | 3 | 2 | 2 | 2 | 10 | 6 | 47 | 11 | ||||||||||||
Q/N | 3 | 1 | 7 | 4 | 347 | 10 | 5 | 4 | 8 | 2 | ||||||||||
Q/P | 1 | 1 | 1 | 1 | 2 | 2 | ||||||||||||||
Q/Q | 1 | 1 | ||||||||||||||||||
Q/R | 229 | 3 | 2 | 2 | ||||||||||||||||
Q/S | 180 | 14 | 721 | 95 | 434 | 73 | 376 | 56 | 1908 | 110 | ||||||||||
Q/T | 3 | 2 | 187 | 1 | 155 | 6 | 247 | 2 | 27 | 4 | ||||||||||
Q/V | 32 | 6 | 26 | 1 | 14 | 3 | 11 | 2 | 37 | 6 | ||||||||||
Q/Y | 2 | 1 | ||||||||||||||||||
R/A | 1 | 1 | ||||||||||||||||||
R/G | 1 | 1 | ||||||||||||||||||
R/S | 1 | 1 | ||||||||||||||||||
S/A | 5 | 1 |