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. 1998 Dec;72(12):10058–10065. doi: 10.1128/jvi.72.12.10058-10065.1998

TABLE 3.

Analysis of P4 properties

Plasmid(s) and temp (°C) Protein(s) produceda ddATPase activityb Aggrega-tivity of P4c Multi-mericity of free P4
pLM662
 18 P1, P2, P4*, P7 0 0 NDd
 28 0 +, ++ ND
pLM1174, -1188, -1223, -1230, -1233, -1242, -1261, -1272 P1, P2, P4*, P7 0 ++ ND
pLM1224 P1, P2, P4*, P7 + 0 +
pAP6 P1, P2, P7 0 ND ND
pLM450 P1, P2, P4, P7 + ND ND
pLM743 P4* 0 ND 0
pLM745
 18 P4* + 0 +
 28 + + +
pJTJ7.3/3, -7.3/7, -7.4/6, -7.5/7 ΔP4 + 0e +e
pJTJ7.5/11, pJTJ7.6/7 ΔP4 0 +e 0e
pAP2 wt P4 + 0 +
a

P4*, mutated P4; ΔP4, truncated P4. 

b

All the mutant and wt P4 cell extracts were analyzed as described in the legend to Fig. 2. Symbols: 0, activity at the same level as that in the control cell extract; +, activity at the same level as that in the wt P4-containing cell extract. No intermediate activities were found. 

c

The relative amount of aggregative P4 was approximated visually for the centrifugation supernatant and pellet by using Western blots. Symbols: ++, ≥90% in aggregate; +, 50% in aggregate; 0, ≤10% in aggregate. 

d

ND, not determined. 

e

These results have been published previously (19).