GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Cloacibacillus porcorum CL-84

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
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component BED41_RS05230 BED41_RS05235
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component BED41_RS05235 BED41_RS14585
ecfT energy-coupling factor transporter, transmembrane (T) component BED41_RS05240
tnaA tryptophanase
Alternative steps:
ackA acetate kinase BED41_RS06145 BED41_RS04200
acs acetyl-CoA synthetase, AMP-forming BED41_RS15085 BED41_RS12210
adh acetaldehyde dehydrogenase (not acylating) BED41_RS11335 BED41_RS08950
ald-dh-CoA acetaldehyde dehydrogenase, acylating BED41_RS11335 BED41_RS04145
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa BED41_RS05620
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
catA catechol 1,2-dioxygenase
catB muconate cycloisomerase
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 BED41_RS14470
mhpD 2-hydroxypentadienoate hydratase BED41_RS05590
mhpE 4-hydroxy-2-oxovalerate aldolase BED41_RS05565
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase BED41_RS15810 BED41_RS00575
nbaF 2-aminomuconate deaminase BED41_RS12990
nbaG 2-oxo-3-hexenedioate decarboxylase BED41_RS05590
pcaD 3-oxoadipate enol-lactone hydrolase
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase BED41_RS10190 BED41_RS01560
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) BED41_RS01550 BED41_RS12320
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) BED41_RS01555 BED41_RS12325
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase BED41_RS15810 BED41_RS00575
praC 2-hydroxymuconate tautomerase BED41_RS03270 BED41_RS14075
praD 2-oxohex-3-enedioate decarboxylase BED41_RS05590
pta phosphate acetyltransferase BED41_RS08975 BED41_RS04165
sibC L-kynurenine 3-monooxygenase
TAT tryptophan permease
tnaB tryptophan:H+ symporter TnaB
tnaT tryptophan:Na+ symporter TnaT BED41_RS12520 BED41_RS11455
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.

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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