L-arabinose catabolism in Paraburkholderia phymatum STM815

GapMind for catabolism of small carbon sources

L-arabinose catabolism in Paraburkholderia phymatum STM815

Best path

araF, araG, araH, xacB, xacC, xacD, xacE, xacF

Rules

Overview: L-arabinose utilization in GapMind is based on MetaCyc pathways L-arabinose degradation I, via xylulose 5-phosphate (link); III, oxidation to 2-oxoglutarate (link); and IV, via glycolaldehyde (link). Pathway II via xylitol and xylulose is not represented in GapMind because it is not reported in prokaryotes (link).

glycolaldehyde-dehydrogenase:

aldA
or aldox-large, aldox-med and aldox-small

all:

arabinose-transport, araA, araB and araD
or arabinose-transport, xacB, xacC, xacD, xacE and xacF
or arabinose-transport, xacB, xacC, xacD, KDG-aldolase, glycolaldehyde-dehydrogenase, gyaR and glcB
Comment: In pathway I, isomerase araA forms L-ribulose, kinase araB forms ribulose 5-phosphate, and epimerase araD forms D-xylulose 5-phosphate, which is an intermediate in the pentose phosphate pathway. In pathway III, the 1-dehydrogenase xacB (which acts on the furanose form, not the usual pyranose form?) forms arabino-1,4-lactone, lactonase xacC forms arbinonate, two dehydratases form 2-dehydro-3-deoxy-L-arabinonate and 2,5-dioxopentanonate (α-ketoglutarate semialdehyde), and dehydrogenase xacF forms 2-oxoglutarate, which is an intermediate in the TCA cycle. (Fitness data suggests that L-arabinose 1-epimerase or mutarotase is also involved, perhaps in creating the correct epimer for the 1-dehydrogenase, but is not included in GapMind.) Pathway IV begins as in pathway III, to 2-dehydro-3-deoxy-L-arabinonate, followed by KDG aldolase to pyruvate and glycolaldehyde; the glycolaldehyde is oxidized to glycolate and then to glyoxylate, and combined with acetyl-CoA by malate synthase, which is a TCA cycle intermediate. (Other pathways for glyxoylate assimilation are known but are not represented here.)

arabinose-transport:

gguA, gguB and chvE
or araF, araG and araH
or araS, araT, araU and araV
or xacG, xacH, xacI, xacJ and xacK
or xylFsa, xylGsa and xylHsa
or araUsh, araVsh, araWsh and araZsh
or araE
or BT0355
or Echvi_1880
Comment: Transporters were identified using query: transporter:arabinose:L-arabinose:L-arabinofuranose:L-arabinopyranose:beta-L-arabinose:CPD-12045:CPD-12046

40 steps (29 with candidates)

Or see definitions of steps

Step	Description	Best candidate	2nd candidate
araF	L-arabinose ABC transporter, substrate-binding component AraF	BPHY_RS13265	BPHY_RS21220
araG	L-arabinose ABC transporter, ATPase component AraG	BPHY_RS13260	BPHY_RS21225
araH	L-arabinose ABC transporter, permease component AraH	BPHY_RS13255	BPHY_RS21230
xacB	L-arabinose 1-dehydrogenase	BPHY_RS21215	BPHY_RS13250
xacC	L-arabinono-1,4-lactonase	BPHY_RS13245	BPHY_RS18670
xacD	L-arabinonate dehydratase	BPHY_RS17490	BPHY_RS33425
xacE	2-dehydro-3-deoxy-L-arabinonate dehydratase	BPHY_RS33410
xacF	alpha-ketoglutarate semialdehyde dehydrogenase	BPHY_RS27205	BPHY_RS32495
Alternative steps:
aldA	(glycol)aldehyde dehydrogenase	BPHY_RS24330	BPHY_RS23210
aldox-large	(glycol)aldehyde oxidoreductase, large subunit	BPHY_RS00465	BPHY_RS22865
aldox-med	(glycol)aldehyde oxidoreductase, medium subunit	BPHY_RS33220	BPHY_RS00460
aldox-small	(glycol)aldehyde oxidoreductase, small subunit	BPHY_RS00470	BPHY_RS33215
araA	L-arabinose isomerase
araB	ribulokinase
araD	L-ribulose-5-phosphate epimerase
araE	L-arabinose:H+ symporter
araS	L-arabinose ABC transporter, substrate-binding component AraS
araT	L-arabinose ABC transporter, permease component 1 (AraT)
araU	L-arabinose ABC transporter, permease component 2 (AraU)
araUsh	L-arabinose ABC transporter, substrate-binding component AraU(Sh)	BPHY_RS27605	BPHY_RS06285
araV	L-arabinose ABC transporter, ATPase component AraV	BPHY_RS36860	BPHY_RS13785
araVsh	L-arabinose ABC transporter, ATPase component AraV(Sh)	BPHY_RS27600	BPHY_RS31570
araWsh	L-arabinose ABC transporter, permease component 1 AraW(Sh)	BPHY_RS27595	BPHY_RS02525
araZsh	L-arabinose ABC transporter, permease component 2 AraZ(Sh)	BPHY_RS27590	BPHY_RS02525
BT0355	L-arabinose:Na+ symporter
chvE	L-arabinose ABC transporter, substrate-binding component ChvE	BPHY_RS11895
Echvi_1880	L-arabinose:Na+ symporter
gguA	L-arabinose ABC transporter, ATPase component GguA	BPHY_RS11890	BPHY_RS31570
gguB	L-arabinose ABC transporter, permease component GguB	BPHY_RS11885	BPHY_RS33915
glcB	malate synthase	BPHY_RS32910	BPHY_RS06960
gyaR	glyoxylate reductase	BPHY_RS04100	BPHY_RS06350
KDG-aldolase	2-dehydro-3-deoxy-L-arabinonate aldolase
xacG	L-arabinose ABC transporter, substrate-binding component XacG
xacH	L-arabinose ABC transporter, permease component 1 (XacH)	BPHY_RS03150
xacI	L-arabinose ABC transporter, permease component 2 (XacI)	BPHY_RS03155
xacJ	L-arabinose ABC transporter, ATPase component 1 (XacJ)	BPHY_RS20430	BPHY_RS03160
xacK	L-arabinose ABC transporter, ATPase component 2 (XacK)	BPHY_RS20430	BPHY_RS13785
xylFsa	L-arabinose ABC transporter, substrate-binding component XylF	BPHY_RS05830
xylGsa	L-arabinose ABC transporter, ATPase component XylG	BPHY_RS05820	BPHY_RS18170
xylHsa	L-arabinose ABC transporter, permease component XylH	BPHY_RS05825	BPHY_RS33915

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.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources