GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Marivita geojedonensis DPG-138

Best path

aroP, kynA, kynB, kyn, antA, antB, antC, catA, catB, catC, pcaD, pcaI, pcaJ, pcaF

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 (26 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP tryptophan:H+ symporter AroP
kynA tryptophan 2,3-dioxygenase MGEO_RS16405
kynB kynurenine formamidase MGEO_RS15860
kyn kynureninase MGEO_RS16410
antA anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AntA MGEO_RS03460
antB anthranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AntB MGEO_RS03465
antC anthranilate 1,2-dioxygenase (deaminating, decarboxylating), electron transfer component AntC MGEO_RS03470
catA catechol 1,2-dioxygenase MGEO_RS03510 MGEO_RS02695
catB muconate cycloisomerase MGEO_RS03455 MGEO_RS06650
catC muconolactone isomerase
pcaD 3-oxoadipate enol-lactone hydrolase MGEO_RS08365 MGEO_RS15960
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) MGEO_RS03530 MGEO_RS07025
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) MGEO_RS03535 MGEO_RS07035
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase MGEO_RS17560 MGEO_RS09905
Alternative steps:
ackA acetate kinase MGEO_RS02500
acs acetyl-CoA synthetase, AMP-forming MGEO_RS21005 MGEO_RS10460
adh acetaldehyde dehydrogenase (not acylating) MGEO_RS02095 MGEO_RS02570
ald-dh-CoA acetaldehyde dehydrogenase, acylating
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa MGEO_RS01925
andAb anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin subunit AndAb MGEO_RS12195
andAc anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AndAc MGEO_RS03460
andAd athranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AndAd
catI 3-oxoadipate CoA-transferase subunit A (CatI)
catJ 3-oxoadipate CoA-transferase subunit B (CatJ)
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component MGEO_RS10190 MGEO_RS02260
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component MGEO_RS16910 MGEO_RS12080
ecfT energy-coupling factor transporter, transmembrane (T) component
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent
mhpD 2-hydroxypentadienoate hydratase
mhpE 4-hydroxy-2-oxovalerate aldolase MGEO_RS00820 MGEO_RS04965
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase MGEO_RS07470 MGEO_RS17260
nbaF 2-aminomuconate deaminase MGEO_RS04115 MGEO_RS08390
nbaG 2-oxo-3-hexenedioate decarboxylase
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase MGEO_RS07470 MGEO_RS17260
praC 2-hydroxymuconate tautomerase
praD 2-oxohex-3-enedioate decarboxylase
pta phosphate acetyltransferase MGEO_RS02495
sibC L-kynurenine 3-monooxygenase
TAT tryptophan permease
tnaA tryptophanase
tnaB tryptophan:H+ symporter TnaB
tnaT tryptophan:Na+ symporter TnaT
trpP energy-coupling factor transporter, tryptophan-specific (S) component TrpP
xylE catechol 2,3-dioxygenase MGEO_RS05310
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.

Links

Downloads

Related tools

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