GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Nitriliruptor alkaliphilus DSM 45188

Best path

tnaT, 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
tnaT tryptophan:Na+ symporter TnaT NITAL_RS18040
tnaA tryptophanase
Alternative steps:
ackA acetate kinase
acs acetyl-CoA synthetase, AMP-forming NITAL_RS15415 NITAL_RS09500
adh acetaldehyde dehydrogenase (not acylating) NITAL_RS23665 NITAL_RS21380
ald-dh-CoA acetaldehyde dehydrogenase, acylating NITAL_RS23725 NITAL_RS13825
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa NITAL_RS03640 NITAL_RS22595
andAb anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin subunit AndAb
andAc anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AndAc NITAL_RS08510
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 NITAL_RS08515
antC anthranilate 1,2-dioxygenase (deaminating, decarboxylating), electron transfer component AntC
aroP tryptophan:H+ symporter AroP
catA catechol 1,2-dioxygenase NITAL_RS00040
catB muconate cycloisomerase NITAL_RS02270
catC muconolactone isomerase
catI 3-oxoadipate CoA-transferase subunit A (CatI) NITAL_RS23510
catJ 3-oxoadipate CoA-transferase subunit B (CatJ) NITAL_RS23515 NITAL_RS12495
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component NITAL_RS02745 NITAL_RS18660
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component NITAL_RS09975 NITAL_RS03290
ecfT energy-coupling factor transporter, transmembrane (T) component
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent
kyn kynureninase NITAL_RS11370
kynA tryptophan 2,3-dioxygenase NITAL_RS24945
kynB kynurenine formamidase NITAL_RS20845 NITAL_RS03280
mhpD 2-hydroxypentadienoate hydratase NITAL_RS23780
mhpE 4-hydroxy-2-oxovalerate aldolase NITAL_RS23730
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase NITAL_RS02765 NITAL_RS05175
nbaF 2-aminomuconate deaminase NITAL_RS11100 NITAL_RS06975
nbaG 2-oxo-3-hexenedioate decarboxylase NITAL_RS23780
pcaD 3-oxoadipate enol-lactone hydrolase NITAL_RS23525 NITAL_RS24855
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase NITAL_RS23530 NITAL_RS08565
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI)
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ)
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase NITAL_RS22635 NITAL_RS04095
praC 2-hydroxymuconate tautomerase
praD 2-oxohex-3-enedioate decarboxylase NITAL_RS23780
pta phosphate acetyltransferase
sibC L-kynurenine 3-monooxygenase NITAL_RS22445
TAT tryptophan permease
tnaB tryptophan:H+ symporter TnaB
trpP energy-coupling factor transporter, tryptophan-specific (S) component TrpP
xylE catechol 2,3-dioxygenase
xylF 2-hydroxymuconate semialdehyde hydrolase NITAL_RS00130 NITAL_RS19805

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 Apr 09 2024. 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