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. 1999 Jul;73(7):5497–5508. doi: 10.1128/jvi.73.7.5497-5508.1999

TABLE 3.

Nef amino acid variations observed during AIDS progression

Patient PBMC sample (mo-yr) No. of clones No. (%) of CD4+ cells No. defec-tivea PxxP Amino acid at position:b
Properties (RP/NP)c NefProg score
15 39 51 102 157 163 169 170 182
FA 9-87 6 537 (29) 2 + T K N Y N S S T E 1/3 −2
11-90 5 266 (14) 0 + T K4R1 N4/T1 Y N S S T E 1/3 −2
5-92 5 32 (2) 1 + T K T3/A1 Y N3/T1 S S3/N1 T E3/Q1 2/2 +0
4-94 9 18 (2) 0 + T R T Y T S8/C1 N T Q 5/1 +4
MB 11-88 12 >1,000 (27) 3 +4/−5 A K8R1 N Y N I/T/S S L5/Q4 E7/V/M 1/2 −1
11-91 7 496 (21) 0 + A R N6/S1 Y T6/N1 I/V/S N Q E/M/Q 6/1 +5
6-93 6 46 (5) 1 + A R N Y T I N Q Q 6/1 +5
3-94 8 64 (5) 1 + A R N Y T I N6/S1 Q Q 6/1 +5
a

Number of clones containing premature stop codons or frameshift mutations (Fig. 6). 

b

Amino acid positions refer to the NL4-3 Nef sequence. Amino acids typically observed in RPs are underlined; amino acids that were more often observed in NPs are in boldface. Subscript numbers are the numbers of individual clones for positions at which sequence variations were observed. Only Nef protein sequences predicted from intact nef open reading frames were included in the analysis. 

c

Number of properties observed more often in RPs and number of properties typically observed in NPs. Numbers were calculated for the representative consensus sequence.