GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Amycolatopsis halophila YIM 93223

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 (28 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP tryptophan:H+ symporter AroP
tnaA tryptophanase AMYHA_RS05440
Alternative steps:
ackA acetate kinase
acs acetyl-CoA synthetase, AMP-forming AMYHA_RS05190 AMYHA_RS07525
adh acetaldehyde dehydrogenase (not acylating) AMYHA_RS13095 AMYHA_RS06610
ald-dh-CoA acetaldehyde dehydrogenase, acylating AMYHA_RS10790
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa AMYHA_RS13120 AMYHA_RS21640
andAb anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin subunit AndAb AMYHA_RS23300
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 AMYHA_RS08935
catA catechol 1,2-dioxygenase AMYHA_RS23850
catB muconate cycloisomerase AMYHA_RS19825
catC muconolactone isomerase
catI 3-oxoadipate CoA-transferase subunit A (CatI) AMYHA_RS23865
catJ 3-oxoadipate CoA-transferase subunit B (CatJ) AMYHA_RS23860
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component AMYHA_RS15620 AMYHA_RS14520
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component AMYHA_RS15620 AMYHA_RS18260
ecfT energy-coupling factor transporter, transmembrane (T) component
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent AMYHA_RS19205
kyn kynureninase AMYHA_RS21195
kynA tryptophan 2,3-dioxygenase AMYHA_RS15300
kynB kynurenine formamidase AMYHA_RS13160
mhpD 2-hydroxypentadienoate hydratase AMYHA_RS06760
mhpE 4-hydroxy-2-oxovalerate aldolase AMYHA_RS10795
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase AMYHA_RS13060 AMYHA_RS13095
nbaF 2-aminomuconate deaminase AMYHA_RS20315
nbaG 2-oxo-3-hexenedioate decarboxylase AMYHA_RS06760
pcaD 3-oxoadipate enol-lactone hydrolase AMYHA_RS23835 AMYHA_RS23830 with AMYHA_RS22055
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase AMYHA_RS23855 AMYHA_RS09650
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI)
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ)
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase AMYHA_RS13060 AMYHA_RS13095
praC 2-hydroxymuconate tautomerase
praD 2-oxohex-3-enedioate decarboxylase AMYHA_RS06760
pta phosphate acetyltransferase
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 AMYHA_RS13065 AMYHA_RS06440
xylF 2-hydroxymuconate semialdehyde hydrolase AMYHA_RS20635 AMYHA_RS06435

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