GapMind for catabolism of small carbon sources

 

L-tryptophan catabolism in Paenisporosarcina indica PN2

Best path

trpP, ecfA1, ecfA2, ecfT, 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 (24 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
trpP energy-coupling factor transporter, tryptophan-specific (S) component TrpP GY23_RS14330
ecfA1 energy-coupling factor transporter, ATPase 1 (A1) component GY23_RS15860 GY23_RS03490
ecfA2 energy-coupling factor transporter, ATPase 2 (A2) component GY23_RS15855 GY23_RS08465
ecfT energy-coupling factor transporter, transmembrane (T) component GY23_RS15850
tnaA tryptophanase
Alternative steps:
ackA acetate kinase
acs acetyl-CoA synthetase, AMP-forming GY23_RS15365 GY23_RS15270
adh acetaldehyde dehydrogenase (not acylating) GY23_RS12590 GY23_RS03610
ald-dh-CoA acetaldehyde dehydrogenase, acylating
andAa anthranilate 1,2-dioxygenase (deaminating, decarboxylating), ferredoxin--NAD(+) reductase component AndAa
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
aroP tryptophan:H+ symporter AroP GY23_RS06985
catA catechol 1,2-dioxygenase GY23_RS08955
catB muconate cycloisomerase GY23_RS08930 GY23_RS12385
catC muconolactone isomerase
catI 3-oxoadipate CoA-transferase subunit A (CatI)
catJ 3-oxoadipate CoA-transferase subunit B (CatJ)
hpaH anthranilate 3-monooxygenase (hydroxylase), FADH2-dependent GY23_RS03700 GY23_RS08870
kyn kynureninase GY23_RS14475
kynA tryptophan 2,3-dioxygenase GY23_RS06780
kynB kynurenine formamidase GY23_RS14470 GY23_RS17145
mhpD 2-hydroxypentadienoate hydratase
mhpE 4-hydroxy-2-oxovalerate aldolase
nbaC 3-hydroxyanthranilate 3,4-dioxygenase
nbaD 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
nbaE 2-aminomuconate 6-semialdehyde dehydrogenase GY23_RS03715 GY23_RS12590
nbaF 2-aminomuconate deaminase GY23_RS16805
nbaG 2-oxo-3-hexenedioate decarboxylase
pcaD 3-oxoadipate enol-lactone hydrolase GY23_RS16375
pcaF succinyl-CoA:acetyl-CoA C-succinyltransferase GY23_RS03620 GY23_RS02485
pcaI 3-oxoadipate CoA-transferase subunit A (PcaI) GY23_RS15565 GY23_RS08940
pcaJ 3-oxoadipate CoA-transferase subunit B (PcaJ) GY23_RS15560 GY23_RS08935
praB 2-hydroxymuconate 6-semialdehyde dehydrogenase GY23_RS03715 GY23_RS03610
praC 2-hydroxymuconate tautomerase GY23_RS06520 GY23_RS12980
praD 2-oxohex-3-enedioate decarboxylase
pta phosphate acetyltransferase GY23_RS06555 GY23_RS04820
sibC L-kynurenine 3-monooxygenase
TAT tryptophan permease
tnaB tryptophan:H+ symporter TnaB
tnaT tryptophan:Na+ symporter TnaT GY23_RS17610
xylE catechol 2,3-dioxygenase GY23_RS11130 GY23_RS07860
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