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. 2014 Jan;88(2):1162–1174. doi: 10.1128/JVI.02262-13

TABLE 1.

Nucleotide sequence of T5 mutations affecting T5 assemblya

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
a

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.

b

Position of the translation termination relative to the total number of amino acids of the wild-type protein.