TABLE 1.
TEM variant | Mutation profile in TEM mutation table | GenBank accession no. | Mutation profile in LacED (derived from GenBank entry)a |
---|---|---|---|
TEM-42 | Q39K, A42V, G238S, E240K, T265M | X98047 | N-3, Q39K, A42V, G238S, E240K, T265M, C-2 |
TEM-59 | Q39K, S130G | AF062386 | Q39K, S130G, C-9 |
TEM-60 | Q39K, L51P, E104K, R164S | AF047171 | Q39K, L51P, E104K, R164S, A187R, S223C, F230L |
TEM-75 | L21F, R164H, T265M | AY130284 | N-12, L21F, R164H, T265M, C-13 |
TEM-89 | Q39K, E104K, S130G, G238S | AY039040 | Q39K, E104K, S130G, G238S, C-8 |
TEM-98 | Empty | AF397068 | S4D, I5P, H289L |
TEM-108 | V80E, G196S, N276S | AF506748 | S4D, I5P, V80E, G196S, N276S |
TEM-117 | L21F | AY130282 | N-12, L21F, C-19 |
TEM-118 | R164H, T265M | AY130285 | N-12, R164H, T265 M, C-13 |
TEM-123 | Q6K, E104K, G238S | AY327539 | Q6K, E104K, G238S, A248-, R275A |
TEM-124 | Q6K, E104K, M182T | AY327540 | Q6K, E104K, M182T, A248-, R275A |
TEM-148 | T189K | AM087454 | T188K |
TEM-187 | L21F, R164H, A184V, T265M | HM246246 | L21F, R164H, A184V, T265M, C-1 |
TEM-191 | E240K | JF949916 | N-10, E240K, C-24 |
TEM-192 | M68I | JF949915 | N-10, M68I, C-25 |
TEM-193 | N136H, L138F, R164C, E166G, E168K, I173T, N175H, M186V, T188N, L220I | JN935135 | N136H, L138F, R164C, E166G, E168K, N170T, N175H, M186V, T188N, L220I |
TEM-199 | Q39K, E104K, M155I, G238S | JX050178 | N-3, Q39K, E104K, M155I, G238S |
TEM-209 | G41A | KF240808 | G41D |
A248-, deletion at position 248. The following abbreviations for differences were used: N-3, missing 3 amino acids at the N terminus; C-2, missing 2 amino acids at the C terminus; Q39K, mutation Q-K at position 39.