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. 1999 Jul;181(13):3904–3911. doi: 10.1128/jb.181.13.3904-3911.1999

TABLE 1.

Kinetic and equilibrium constants of AcPhe-puromycin synthesis carried out in the presence of spermine analogues, with complex C formed in the absence of the FWR fraction

Effectora k3b (min−1) Ksb (μM) Kic (μM) βc
None (control) 1.11 660
SPM 118 0.165
N1-MESPM 138 0.138
N1,N12-BESPM 225 0.360
N4,N9-BESPM 222 0.345
N4,N9-DBzSPM 130 0.522
a

SPM, spermine; N1-MESPM, N1-ethylspermine; N1,N12-BESPM, N1,N12-bis(ethyl)spermine; N4,N9-BESPM, N4,N9-bis(ethyl)spermine; N4,N9-DBzSPM, N4,N9-dibenzylspermine. 

b

The k3 and Ks values were calculated by fitting the experimental data to equation 2 by a least-square procedure provided by Microcal Software, Inc. 

c

The Ki and β values were obtained from the corresponding 1/Δ intercept replots.