Table 1.
Basic amino acids identified as candidate mediators of IP6-binding by Ku—Ku70 sequence alignment
| Human | Mouse | Rat | Hamster | Chicken | Xenopus | Zebrafish | S. pombe | S. cerevisiae |
|---|---|---|---|---|---|---|---|---|
| K 357 | K | K | K | K | K | K | K | H |
| K 358 | K | N | K | Q | K | L | P | Y |
| K 443 | K | K | K | K | I | I | I | I |
| R 444 | R | R | R | R | R | R | R | R |
| K 445 | K | K | K | N | K | T | S | K |
Accession numbers for the Ku70 amino acid sequences—Human, AAH12154; mouse, BAA28874; rat, AAH78718; hamster, AAB46854; chicken, BAA32018; Xenopus, NP_001082274; zebrafish, ABI54461; S. pombe, O94395; S. cerevisiae, P32807. Multiple sequence alignment was done using Clustal W (1.83). Amino acids that may participate in IP6 binding by human Ku and the corresponding residues of other species as shown. Basic amino acids (lysines, K or arginines, R) are in bold. Lysine residues mutated in this study are underlined.