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. 1998 May 18;141(4):917–927. doi: 10.1083/jcb.141.4.917

Table I.

Construction of Recombinant Wild-Type and Chimeric Toxins

Clone Toxin or chimera A1 subunit Junction A2 subunit B subunit
pMGJ148 CT (native) CTA1 CGNAP R*SSMSNTC CTA2-CTB
187     199
pMGJ179 CTA/LTIIbB CTA1 CGNAP R*SSMDTTC LTIIbA2-LTIIbB
187     197
pMGJ183 LTIIb(S193M) LTIIbA1 CLPNN*KASMDTTC LTIIb A2-LTIIbB
185     197
pMGJ184 LTIIbA/CTB LTIIbA1 CLPNN*KASMSNTC CT A2-CTB
185     199
pMGJ187 LTIIbA/CTB LTIIbA1    KKYIKRQIFF LTIIbA2::CTA2-CTB
   213     224

Amino acid sequences of the junctions formed between A1 and A2 peptides are shown in letter code. Numbers beneath cysteines indicate the position in the native protein. In the native protein these cysteines are linked by disulfhydryl bond.  

*

 above the letter codes identifies the serine-protease cleavage site linking the A1 and A2 peptides. The cleavage site for pMGJ187 is the same as for native LTIIb and the fusion joint (underlined) is within the A2 domain instead of between the A1 and A2 domains.