Table 1. Filter binding assays with human and B. burgdorferi Pur-α.
Protein | ssDNA 12mer | Sequence 5′ – 3′ | KDs [nM] | Avg. KDs [nM] |
Human Pur-α 56–287 (C272S) | hTel12 | (AGG GTT)2 | 491, 438, 306 | 411±95 |
B. burgdorferi Pur-α 6–127 | hTel12 | (AGG GTT)2 | 435, 445, 413, 413 | 426±16 |
Human Pur-α 56–287 (C272S) | JCVupTAR | GGA GGG GGA GGC | 207, 258 | 233±36 |
B. burgdorferi Pur-α 6–127 | JCVupTAR | GGA GGG GGA GGC | 395, 428, 521, 533 | 469±68 |
Human Pur-α 56–287 (C272S) | Control | CCT CCG CCT CCG | No binding | No binding |
B. burgdorferi Pur-α 6–127 | Control | CCT CCG CCT CCG | No binding | No binding |
Equilibrium dissociation constants (KD) from filter binding experiments. C272S in protein name indicates that the cysteine in amino acid position 272 was mutated to serine.