GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Bacillus velezensis CBMB205

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 (22 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
trpP energy-coupling factor transporter, tryptophan-specific (S) component TrpP AAV34_RS14345
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component AAV34_RS18595 AAV34_RS17845
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component AAV34_RS18590 AAV34_RS08140
ecfT energy-coupling factor transporter, transmembrane (T) component AAV34_RS18585
tnaA tryptophanase
Alternative steps:
ackA acetate kinase AAV34_RS05960 AAV34_RS18120
acs acetyl-CoA synthetase, AMP-forming AAV34_RS05745 AAV34_RS05915
adh acetaldehyde dehydrogenase (not acylating) AAV34_RS09750 AAV34_RS00625
ald-dh-CoA acetaldehyde dehydrogenase, acylating
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa AAV34_RS17700
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 AAV34_RS05395 AAV34_RS18265
catA catechol 1,2-dioxygenase
catB muconate cycloisomerase AAV34_RS12895
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 AAV34_RS18165
kyn kynureninase
kynA tryptophan 2,3-dioxygenase
kynB kynurenine formamidase
mhpD 2-hydroxypentadienoate hydratase
mhpE 4-hydroxy-2-oxovalerate aldolase AAV34_RS06505
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase AAV34_RS09750 AAV34_RS05095
nbaF 2-aminomuconate deaminase AAV34_RS15960 AAV34_RS19170
nbaG 2-oxo-3-hexenedioate decarboxylase
pcaD 3-oxoadipate enol-lactone hydrolase
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase AAV34_RS04175 AAV34_RS08045
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) AAV34_RS10165 AAV34_RS09505
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) AAV34_RS10170 AAV34_RS09510
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase AAV34_RS09750 AAV34_RS05095
praC 2-hydroxymuconate tautomerase AAV34_RS01730
praD 2-oxohex-3-enedioate decarboxylase
pta phosphate acetyltransferase AAV34_RS01635 AAV34_RS08085
sibC L-kynurenine 3-monooxygenase
TAT tryptophan permease AAV34_RS01580 AAV34_RS00835
tnaB tryptophan:H+ symporter TnaB
tnaT tryptophan:Na+ symporter TnaT
xylE catechol 2,3-dioxygenase AAV34_RS15310
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