EC Number   |
Protein Variants |
Reference |
|---|
   4.1.99.19 | A26G |
the thiH mutant allele results in a phenotype with thiamine auxotrophy that is corrected by either L-tyrosine or thiazole |
715471 |
| 4.1.99.19 | A272V |
the thiH mutant allele results in a thiH null phenotype |
715471 |
| 4.1.99.19 | A373P |
the thiH mutant allele results in a phenotype with thiamine auxotrophy that is corrected by either L-tyrosine or thiazole |
715471 |
| 4.1.99.19 | A50T |
the thiH mutant allele results in a thiH null phenotype |
715471 |
| 4.1.99.19 | A51V |
the thiH mutant allele results in a phenotype with thiamine auxotrophy that is corrected by either L-tyrosine or thiazole |
715471 |
| 4.1.99.19 | A61A |
the thiH mutant allele results in a phenotype with thiamine auxotrophy that is corrected by either L-tyrosine or thiazole |
715471 |
| 4.1.99.19 | A61T |
the thiH mutant allele results in a thiH null phenotype |
715471 |
| 4.1.99.19 | C285A |
the thiH mutant allele results in a phenotype with thiamine auxotrophy that is corrected by either L-tyrosine or thiazole |
715471 |
| 4.1.99.19 | C285H |
the thiH mutant allele results in a thiH null phenotype |
715471 |
| 4.1.99.19 | C89A |
the thiH mutant allele results in a thiH null phenotype |
715471 |
