GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Dyella jiangningensis SBZ3-12

Best path

aroP, kynA, kynB, sibC, kyn, nbaC, nbaD, nbaE, nbaF, nbaG, mhpD, mhpE, adh, acs

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 (24 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP tryptophan:H+ symporter AroP BLQ78_RS08805 BLQ78_RS03050
kynA tryptophan 2,3-dioxygenase BLQ78_RS11975
kynB kynurenine formamidase BLQ78_RS00605
sibC L-kynurenine 3-monooxygenase BLQ78_RS17235
kyn kynureninase BLQ78_RS15195
nbaC 3-hydroxyanthranilate 3,4-dioxygenase BLQ78_RS06290
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase BLQ78_RS15185
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase BLQ78_RS22185 BLQ78_RS02465
nbaF 2-aminomuconate deaminase BLQ78_RS22195 BLQ78_RS11670
nbaG 2-oxo-3-hexenedioate decarboxylase
mhpD 2-hydroxypentadienoate hydratase
mhpE 4-hydroxy-2-oxovalerate aldolase
adh acetaldehyde dehydrogenase (not acylating) BLQ78_RS18120 BLQ78_RS22185
acs acetyl-CoA synthetase, AMP-forming BLQ78_RS13905 BLQ78_RS05135
Alternative steps:
ackA acetate kinase BLQ78_RS18285 BLQ78_RS21345
ald-dh-CoA acetaldehyde dehydrogenase, acylating
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa BLQ78_RS02470
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 BLQ78_RS10550
catA catechol 1,2-dioxygenase
catB muconate cycloisomerase BLQ78_RS02265
catC muconolactone isomerase
catI 3-oxoadipate CoA-transferase subunit A (CatI)
catJ 3-oxoadipate CoA-transferase subunit B (CatJ)
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component BLQ78_RS06240 BLQ78_RS18995
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component BLQ78_RS18995 BLQ78_RS06240
ecfT energy-coupling factor transporter, transmembrane (T) component
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent
pcaD 3-oxoadipate enol-lactone hydrolase BLQ78_RS14530
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase BLQ78_RS03030 BLQ78_RS14050
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) BLQ78_RS09600
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) BLQ78_RS09600
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase BLQ78_RS22185 BLQ78_RS02465
praC 2-hydroxymuconate tautomerase
praD 2-oxohex-3-enedioate decarboxylase
pta phosphate acetyltransferase BLQ78_RS00180
TAT tryptophan permease BLQ78_RS08805
tnaA tryptophanase
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

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