GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Bacillus altitudinis 41KF2b

Best path

trpP, ecfA1, ecfA2, ecfT, tnaA

Rules

Overview: Tryptophan degradation in GapMind is based on MetaCyc degradation pathways I via anthranilate (link), II via pyruvate (link), or IX via 3-hydroxyanthranilate (link). Pathway XII (link) overlaps with pathway I and is also represented. The other MetaCyc pathways do not yield fixed carbon or are not reported in prokaryotes, and are not included. For example, pathway IV yields indole-3-lactate, which could potentially be oxidized to indole-3-acetate, which has a known catabolic pathway, but no prokaryotes are known to consume tryptophan this way. Pathway VIII yields tryptophol (also known as indole-3-ethanol), which could potentially be oxidized to indole-3-acetate and consumed. Pathways X and XIII yield indole-3-propionate, which may spontaneously oxidize to kynurate, but kynurate catabolism is not reported.

47 steps (20 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
trpP energy-coupling factor transporter, tryptophan-specific (S) component TrpP BA79_RS14245
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component BA79_RS16260 BA79_RS17265
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component BA79_RS16265 BA79_RS15935
ecfT energy-coupling factor transporter, transmembrane (T) component BA79_RS16270
tnaA tryptophanase
Alternative steps:
ackA acetate kinase BA79_RS07620
acs acetyl-CoA synthetase, AMP-forming BA79_RS07825 BA79_RS18200
adh acetaldehyde dehydrogenase (not acylating) BA79_RS13175 BA79_RS15800
ald-dh-CoA acetaldehyde dehydrogenase, acylating
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa BA79_RS12940
andAb anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin subunit AndAb
andAc anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AndAc
andAd athranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AndAd
antA anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AntA
antB anthranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AntB
antC anthranilate 1,2-dioxygenase (deaminating, decarboxylating), electron transfer component AntC
aroP tryptophan:H+ symporter AroP BA79_RS12105 BA79_RS14470
catA catechol 1,2-dioxygenase
catB muconate cycloisomerase BA79_RS01190
catC muconolactone isomerase
catI 3-oxoadipate CoA-transferase subunit A (CatI)
catJ 3-oxoadipate CoA-transferase subunit B (CatJ)
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent
kyn kynureninase
kynA tryptophan 2,3-dioxygenase
kynB kynurenine formamidase
mhpD 2-hydroxypentadienoate hydratase
mhpE 4-hydroxy-2-oxovalerate aldolase
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase BA79_RS13175 BA79_RS04010
nbaF 2-aminomuconate deaminase BA79_RS16795
nbaG 2-oxo-3-hexenedioate decarboxylase
pcaD 3-oxoadipate enol-lactone hydrolase
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase BA79_RS04980 BA79_RS09045
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) BA79_RS14645
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) BA79_RS14650
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase BA79_RS13175 BA79_RS04010
praC 2-hydroxymuconate tautomerase BA79_RS09135
praD 2-oxohex-3-enedioate decarboxylase
pta phosphate acetyltransferase BA79_RS09250 BA79_RS11095
sibC L-kynurenine 3-monooxygenase
TAT tryptophan permease BA79_RS15915 BA79_RS14470
tnaB tryptophan:H+ symporter TnaB
tnaT tryptophan:Na+ symporter TnaT
xylE catechol 2,3-dioxygenase BA79_RS09795
xylF 2-hydroxymuconate semialdehyde hydrolase

Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory