GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Novosphingobium lindaniclasticum LE124

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 (32 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP tryptophan:H+ symporter AroP L284_RS38990 L284_RS39000
tnaA tryptophanase
Alternative steps:
ackA acetate kinase L284_RS31805
acs acetyl-CoA synthetase, AMP-forming L284_RS28260 L284_RS38215
adh acetaldehyde dehydrogenase (not acylating) L284_RS43410 L284_RS35235
ald-dh-CoA acetaldehyde dehydrogenase, acylating L284_RS38045
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa L284_RS44520 L284_RS44895
andAb anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin subunit AndAb L284_RS37145 L284_RS36750
andAc anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AndAc L284_RS37140
andAd athranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AndAd
antA anthranilate 1,2-dioxygenase (deaminating, decarboxylating), large subunit AntA L284_RS28860
antB anthranilate 1,2-dioxygenase (deaminating, decarboxylating), small subunit AntB
antC anthranilate 1,2-dioxygenase (deaminating, decarboxylating), electron transfer component AntC
catA catechol 1,2-dioxygenase L284_RS36700 L284_RS46895
catB muconate cycloisomerase L284_RS36710
catC muconolactone isomerase L284_RS36705
catI 3-oxoadipate CoA-transferase subunit A (CatI) L284_RS38015
catJ 3-oxoadipate CoA-transferase subunit B (CatJ) L284_RS38010
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component L284_RS42365 L284_RS25720
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component L284_RS25720 L284_RS42365
ecfT energy-coupling factor transporter, transmembrane (T) component
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent
kyn kynureninase L284_RS25380
kynA tryptophan 2,3-dioxygenase L284_RS25385
kynB kynurenine formamidase
mhpD 2-hydroxypentadienoate hydratase L284_RS38040
mhpE 4-hydroxy-2-oxovalerate aldolase L284_RS38050
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase L284_RS43410 L284_RS38635
nbaF 2-aminomuconate deaminase L284_RS42250
nbaG 2-oxo-3-hexenedioate decarboxylase L284_RS38040
pcaD 3-oxoadipate enol-lactone hydrolase L284_RS36685
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase L284_RS36680 L284_RS37150
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) L284_RS36695 L284_RS29445
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) L284_RS36690 L284_RS29450
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase L284_RS43410 L284_RS35235
praC 2-hydroxymuconate tautomerase
praD 2-oxohex-3-enedioate decarboxylase L284_RS38040
pta phosphate acetyltransferase L284_RS35885
sibC L-kynurenine 3-monooxygenase
TAT tryptophan permease L284_RS39000 L284_RS38240
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 L284_RS38035

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