GapMind for catabolism of small carbon sources

 

L-phenylalanine catabolism in Granulicella mallensis MP5ACTX8

Best path

aroP, PAH, PCBD, QDPR, HPD, hmgA, maiA, fahA, atoA, atoD, atoB

Rules

Overview: Phenylalanine utilization in GapMind is based on MetaCyc pathway L-phenylalanine degradation I (aerobic, via tyrosine, link), pathway II (anaerobic, via phenylacetaldehyde dehydrogenase, link), degradation via phenylpyruvate:ferredoxin oxidoreductase (PMC3346364), or degradation via phenylacetaldehyde:ferredoxin oxidoreductase (PMID:24214948). (MetaCyc describes additional pathways, but they do not result in carbon incorporation or are not reported in prokaryotes, so they are not included in GapMind.)

76 steps (30 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP L-phenylalanine:H+ symporter AroP
PAH phenylalanine 4-monooxygenase ACIX8_RS13750
PCBD pterin-4-alpha-carbinoalamine dehydratase ACIX8_RS11795
QDPR 6,7-dihydropteridine reductase
HPD 4-hydroxyphenylpyruvate dioxygenase ACIX8_RS03140
hmgA homogentisate dioxygenase ACIX8_RS03535
maiA maleylacetoacetate isomerase
fahA fumarylacetoacetate hydrolase ACIX8_RS03125 ACIX8_RS00420
atoA acetoacetyl-CoA transferase, A subunit ACIX8_RS23700
atoD acetoacetyl-CoA transferase, B subunit ACIX8_RS23705
atoB acetyl-CoA C-acetyltransferase ACIX8_RS05900
Alternative steps:
aacS acetoacetyl-CoA synthetase
ARO10 phenylpyruvate decarboxylase
ARO8 L-phenylalanine transaminase ACIX8_RS10465 ACIX8_RS20780
badH 2-hydroxy-cyclohexanecarboxyl-CoA dehydrogenase ACIX8_RS01400 ACIX8_RS00605
badI 2-ketocyclohexanecarboxyl-CoA hydrolase ACIX8_RS18945 ACIX8_RS02780
badK cyclohex-1-ene-1-carboxyl-CoA hydratase ACIX8_RS02780 ACIX8_RS18945
bamB class II benzoyl-CoA reductase, BamB subunit
bamC class II benzoyl-CoA reductase, BamC subunit
bamD class II benzoyl-CoA reductase, BamD subunit
bamE class II benzoyl-CoA reductase, BamE subunit
bamF class II benzoyl-CoA reductase, BamF subunit
bamG class II benzoyl-CoA reductase, BamG subunit
bamH class II benzoyl-CoA reductase, BamH subunit
bamI class II benzoyl-CoA reductase, BamI subunit
bcrA ATP-dependent benzoyl-CoA reductase, alpha subunit
bcrB ATP-dependent benzoyl-CoA reductase, beta subunit
bcrC ATP-dependent benzoyl-CoA reductase, gamma subunit
bcrD ATP-dependent benzoyl-CoA reductase, delta subunit
boxA benzoyl-CoA epoxidase, subunit A
boxB benzoyl-CoA epoxidase, subunit B
boxC 2,3-epoxybenzoyl-CoA dihydrolase
boxD 3,4-dehydroadipyl-CoA semialdehyde dehydrogenase
Ch1CoA cyclohex-1-ene-1-carbonyl-CoA dehydrogenase ACIX8_RS10450 ACIX8_RS18780
dch cyclohexa-1,5-diene-1-carboxyl-CoA hydratase ACIX8_RS18945 ACIX8_RS02780
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase ACIX8_RS02780 ACIX8_RS18945
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase ACIX8_RS10250 ACIX8_RS18095
gcdH glutaryl-CoA dehydrogenase ACIX8_RS10450 ACIX8_RS18780
had 6-hydroxycyclohex-1-ene-1-carbonyl-CoA dehydrogenase
iorA phenylpyruvate:ferredoxin oxidoreductase, IorA subunit
iorAB phenylpyruvate:ferredoxin oxidoreductase, fused IorA/IorB
iorB phenylpyruvate:ferredoxin oxidoreductase, IorB subunit
livF L-phenylalanine ABC transporter, ATPase component 1 (LivF) ACIX8_RS09470 ACIX8_RS04120
livG L-phenylalanine ABC transporter, ATPase component 2 (LivG) ACIX8_RS09470 ACIX8_RS20045
livH L-phenylalanine ABC transporter, permease component 1 (LivH)
livJ L-phenylalanine ABC transporter, substrate-binding component LivJ/LivK
livM L-phenylalanine ABC transporter, permease component 2 (LivM)
oah 6-oxocyclohex-1-ene-1-carbonyl-CoA hydratase
paaA phenylacetyl-CoA 1,2-epoxidase, subunit A
paaB phenylacetyl-CoA 1,2-epoxidase, subunit B
paaC phenylacetyl-CoA 1,2-epoxidase, subunit C
paaE phenylacetyl-CoA 1,2-epoxidase, subunit E
paaF 2,3-dehydroadipyl-CoA hydratase ACIX8_RS02780 ACIX8_RS18945
paaG 1,2-epoxyphenylacetyl-CoA isomerase / 2-(oxepinyl)acetyl-CoA isomerase / didehydroadipyl-CoA isomerase ACIX8_RS18945 ACIX8_RS02780
paaH 3-hydroxyadipyl-CoA dehydrogenase ACIX8_RS10250 ACIX8_RS18095
paaJ1 3-oxo-5,6-dehydrosuberyl-CoA thiolase ACIX8_RS05900
paaJ2 3-oxoadipyl-CoA thiolase ACIX8_RS05900
paaK phenylacetate-CoA ligase
paaZ1 oxepin-CoA hydrolase ACIX8_RS18945
paaZ2 3-oxo-5,6-didehydrosuberyl-CoA semialdehyde dehydrogenase
pad-dh phenylacetaldehyde dehydrogenase ACIX8_RS16850 ACIX8_RS07595
padB phenylacetyl-CoA dehydrogenase, PadB subunit
padC phenylacetyl-CoA dehydrogenase, PadC subunit ACIX8_RS00885 ACIX8_RS04440
padD phenylacetyl-CoA dehydrogenase, PadD subunit
padE phenylglyoxylate dehydrogenase, gamma subunit
padF phenylglyoxylate dehydrogenase, delta subunit
padG phenylglyoxylate dehydrogenase, alpha subunit
padH phenylglyoxylate dehydrogenase, epsilon subunit
padI phenylglyoxylate dehydrogenase, beta subunit
pfor phenylacetaldeyde:ferredoxin oxidoreductase
pimB 3-oxopimeloyl-CoA:CoA acetyltransferase ACIX8_RS05900
pimC pimeloyl-CoA dehydrogenase, small subunit
pimD pimeloyl-CoA dehydrogenase, large subunit
pimF 6-carboxyhex-2-enoyl-CoA hydratase
PPDCalpha phenylpyruvate decarboxylase, alpha subunit ACIX8_RS06540
PPDCbeta phenylpyruvate decarboxylase, beta subunit ACIX8_RS06540

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