Component_35638 |
trp operon repressor |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_13 |
TIGR00565 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_87 |
tryptophan synthase, beta subunit |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_48005 |
TIGR01321 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_85 |
anthranilate synthase component I |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Component_90 |
anthranilate phosphoribosyltransferase |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_16 |
TIGR00263 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_14 |
TIGR01815 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_161 |
anthranilate synthase component II |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_17 |
TIGR01415 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0037 |
tryptophan biosynthesis from ribose-5-phosphate~The essential amino acid tryptophan is synthesized in prokaryotes, plants, and fungi via a conserved six step pathway from the branchpoint compound chrosimate, a common precursor in the biosynthesis of aromatic amino acids [1]. Seven catalytic domains and two alpha/beta subunit complexes comprise this pathway. Individually expressed in some organisms, gene fusions encoding single proteins possessing two or more of these catalytic domains have been observed for every trp gene. Although the occurance of gene fusions have been shown to be phylogenetically unrelated, a conserved gene order can be discerned within the domain Bacteria. Occasionally gene(s) dissociations disrupt gene order as in Campylobacter jejuni and Deinococcus radiodurans, or the pathway is found split between two separate chromosomes as in Rhodobacter sphaeroides. In cyanobacteria, such as Nostoc and Anabaena, it is not uncommon to observe paralogous trp genes as part of a larger 'supraoperon' including other aromatic amino acid synthesizing genes as well as their trp counterparts [2]. |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_18 |
TIGR00262 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Component_91 |
N-(5'phosphoribosyl)anthranilate isomerase |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_137 |
TIGR00566 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_2374 |
TIGR01919 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_15 |
TIGR01820 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_19 |
PF00218 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Component_89 |
indole-3-glycerol phosphate synthase |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_12 |
TIGR00564 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_21 |
PF00697 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_53104 |
TIGR01251 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Component_88 |
tryptophan synthase, alpha subunit |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Evidence_20 |
TIGR01245 HMM |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|
Component_40735 |
ribose-phosphate pyrophosphokinase |
True - {{t}} |
True - {{t}} |
Confirmed presence |
|