GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Marinobacter psychrophilus 20041

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 (24 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP tryptophan:H+ symporter AroP
kynA tryptophan 2,3-dioxygenase
kynB kynurenine formamidase
kyn kynureninase
antA anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AntA ABA45_RS01240
antB anthranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AntB ABA45_RS01245
antC anthranilate 1,2-dioxygenase (deaminating, decarboxylating), electron transfer component AntC ABA45_RS01250
catA catechol 1,2-dioxygenase ABA45_RS01235
catB muconate cycloisomerase ABA45_RS01225
catC muconolactone isomerase ABA45_RS01230
pcaD 3-oxoadipate enol-lactone hydrolase ABA45_RS01195
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) ABA45_RS05665 ABA45_RS07425
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) ABA45_RS05660 ABA45_RS07430
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase ABA45_RS15050 ABA45_RS15615
Alternative steps:
ackA acetate kinase ABA45_RS06545 ABA45_RS08060
acs acetyl-CoA synthetase, AMP-forming ABA45_RS12430 ABA45_RS11005
adh acetaldehyde dehydrogenase (not acylating) ABA45_RS06205 ABA45_RS15565
ald-dh-CoA acetaldehyde dehydrogenase, acylating
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa ABA45_RS16830
andAb anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin subunit AndAb
andAc anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AndAc ABA45_RS01240
andAd athranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AndAd
catI 3-oxoadipate CoA-transferase subunit A (CatI) ABA45_RS01210
catJ 3-oxoadipate CoA-transferase subunit B (CatJ) ABA45_RS01205
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component ABA45_RS01310 ABA45_RS16135
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component ABA45_RS14720 ABA45_RS07060
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 ABA45_RS03455
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase ABA45_RS14435 ABA45_RS06205
nbaF 2-aminomuconate deaminase ABA45_RS09540 ABA45_RS12815
nbaG 2-oxo-3-hexenedioate decarboxylase
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase ABA45_RS14435 ABA45_RS06205
praC 2-hydroxymuconate tautomerase
praD 2-oxohex-3-enedioate decarboxylase
pta phosphate acetyltransferase ABA45_RS08055
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
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