TABLE 1.
Name | Gene/protein affected | Phenotype | Mutation | Stop codon positionb | Reference |
---|---|---|---|---|---|
T5D17am34d | D17 (T5p133), tail protein pb4 | Filled mature head | C268T | 90/689 | 34 |
T5D20am30d | D20 (T5p145), major head protein pb8 | Functional tail | C1132T | 378/459 | 34 |
T5amN5 | T5p151, terminase large subunit | Empty prohead II | C1189T | 397/439 | 8 |
T5amHA911 | T5p149, nicking endonuclease | Nick-less DNA | C337T | 118/151 | 43 |
T5hd1 | ltf, L-shaped fiber protein | High density | +T873 | 304/1396 | 13 |
Mapping of the mutations was determined by sequencing the late gene region of each T5 mutant genome: 6-kbp fragments amplified by PCR from purified T5 mutant DNA were sequenced using primers designed from the T5st0 genome sequence. In amber mutants, the Stop codon results from a point mutation. In T5hd1, the Stop codon results from an insertion (+) that alters the normal reading frame.
Position of the translation termination relative to the total number of amino acids of the wild-type protein.