GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Azospirillum thiophilum BV-S

Best path

aroP, 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 (27 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP tryptophan:H+ symporter AroP
tnaA tryptophanase
Alternative steps:
ackA acetate kinase AL072_RS27185 AL072_RS00850
acs acetyl-CoA synthetase, AMP-forming AL072_RS06780 AL072_RS08155
adh acetaldehyde dehydrogenase (not acylating) AL072_RS23920 AL072_RS26875
ald-dh-CoA acetaldehyde dehydrogenase, acylating AL072_RS26875
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa AL072_RS31205
andAb anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin subunit AndAb
andAc anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AndAc AL072_RS30310
andAd athranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AndAd
antA anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AntA AL072_RS30310
antB anthranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AntB
antC anthranilate 1,2-dioxygenase (deaminating, decarboxylating), electron transfer component AntC AL072_RS26905
catA catechol 1,2-dioxygenase AL072_RS23745
catB muconate cycloisomerase
catC muconolactone isomerase
catI 3-oxoadipate CoA-transferase subunit A (CatI) AL072_RS23775
catJ 3-oxoadipate CoA-transferase subunit B (CatJ) AL072_RS23770
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component AL072_RS17005 AL072_RS25645
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component AL072_RS18480 AL072_RS18150
ecfT energy-coupling factor transporter, transmembrane (T) component
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent
kyn kynureninase
kynA tryptophan 2,3-dioxygenase
kynB kynurenine formamidase
mhpD 2-hydroxypentadienoate hydratase AL072_RS30400
mhpE 4-hydroxy-2-oxovalerate aldolase
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase AL072_RS18935
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase AL072_RS26660 AL072_RS23920
nbaF 2-aminomuconate deaminase AL072_RS17505 AL072_RS13955
nbaG 2-oxo-3-hexenedioate decarboxylase AL072_RS30400
pcaD 3-oxoadipate enol-lactone hydrolase AL072_RS23760 AL072_RS17745
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase AL072_RS16305 AL072_RS22420
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) AL072_RS23380 AL072_RS21860
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) AL072_RS21865 AL072_RS23385
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase AL072_RS26660 AL072_RS23920
praC 2-hydroxymuconate tautomerase AL072_RS12240
praD 2-oxohex-3-enedioate decarboxylase AL072_RS30400
pta phosphate acetyltransferase AL072_RS27180 AL072_RS00855
sibC L-kynurenine 3-monooxygenase
TAT tryptophan permease
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 AL072_RS27655

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