GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Limnohabitans curvus MWH-C5

Best path

braC, braD, braE, braF, braG, tdcB, tdcE, pccA, pccB, epi, mcm-large, mcm-small

Rules

Overview: L-threonine degradation in GapMind is based on MetaCyc pathway I via 2-ketobutyrate formate-lyase (link), pathway II via glycine (link), pathway III via methylglyoxal (link), and pathway IV via threonine aldolase (link). Pathway V is not thought to occur in prokaryotes and is not included.

70 steps (41 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
braC L-alanine/L-serine/L-threonine ABC transporter, substrate binding protein (BraC/NatB) B9Z44_RS00730
braD L-alanine/L-serine/L-threonine ABC transporter, permease component 1 (BraD/NatD) B9Z44_RS04225 B9Z44_RS05730
braE L-alanine/L-serine/L-threonine ABC transporter, permease component 2 (BraE/NatC) B9Z44_RS04220 B9Z44_RS12865
braF L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 1 (BraF/NatA) B9Z44_RS12870 B9Z44_RS04215
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) B9Z44_RS12875 B9Z44_RS05720
tdcB L-threonine dehydratase B9Z44_RS09005
tdcE 2-ketobutyrate formate-lyase
pccA propionyl-CoA carboxylase, alpha subunit B9Z44_RS12515 B9Z44_RS05480
pccB propionyl-CoA carboxylase, beta subunit B9Z44_RS12510 B9Z44_RS05490
epi methylmalonyl-CoA epimerase B9Z44_RS12520
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit B9Z44_RS12500 B9Z44_RS08505
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit B9Z44_RS12500
Alternative steps:
ackA acetate kinase B9Z44_RS09890
acn (2R,3S)-2-methylcitrate dehydratase B9Z44_RS03110
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
acs acetyl-CoA synthetase, AMP-forming B9Z44_RS10305 B9Z44_RS13605
adh acetaldehyde dehydrogenase (not acylating) B9Z44_RS11745 B9Z44_RS11550
ald-dh-CoA acetaldehyde dehydrogenase, acylating
aldA lactaldehyde dehydrogenase B9Z44_RS11550 B9Z44_RS11745
D-LDH D-lactate dehydrogenase B9Z44_RS07465 B9Z44_RS02025
dddA 3-hydroxypropionate dehydrogenase B9Z44_RS07885 B9Z44_RS05710
DVU3032 L-lactate dehydrogenase, LutC-like component
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components
gcvH glycine cleavage system, H component (lipoyl protein) B9Z44_RS11595
gcvP glycine cleavage system, P component (glycine decarboxylase)
gcvT glycine cleavage system, T component (tetrahydrofolate aminomethyltransferase)
glcD D-lactate dehydrogenase, FAD-linked subunit 1 (GlcD) B9Z44_RS08195 B9Z44_RS07465
glcE D-lactate dehydrogenase, FAD-linked subunit 2 (GlcE) B9Z44_RS07580 B9Z44_RS07465
glcF D-lactate dehydrogenase, FeS subunit GlcF B9Z44_RS07585
gloA glyoxylase I B9Z44_RS11935
gloB hydroxyacylglutathione hydrolase (glyoxalase II) B9Z44_RS00515 B9Z44_RS07720
grdA glycine reductase component A1
grdB glycine reductase component B, gamma subunit
grdC glycine reductase component C, beta subunit
grdD glycine reductase component C, alpha subunit
grdE glycine reductase component B, precursor to alpha/beta subunits
hpcD 3-hydroxypropionyl-CoA dehydratase B9Z44_RS10090 B9Z44_RS01330
iolA malonate semialdehyde dehydrogenase (CoA-acylating) B9Z44_RS07890 B9Z44_RS11745
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase)
L-LDH L-lactate dehydrogenase B9Z44_RS04070
lctB electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), small subunit
lctC electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), large subunit B9Z44_RS11375 B9Z44_RS01310
lctD D-lactate dehydrogenase (NAD+, ferredoxin), lactate dehydrogenase component B9Z44_RS08195 B9Z44_RS07465
lctO L-lactate oxidase or 2-monooxygenase B9Z44_RS04070
lldE L-lactate dehydrogenase, LldE subunit
lldF L-lactate dehydrogenase, LldF subunit
lldG L-lactate dehydrogenase, LldG subunit
lpd dihydrolipoyl dehydrogenase B9Z44_RS13470 B9Z44_RS13620
ltaE L-threonine aldolase B9Z44_RS01900
lutA L-lactate dehydrogenase, LutA subunit
lutB L-lactate dehydrogenase, LutB subunit
lutC L-lactate dehydrogenase, LutC subunit
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components B9Z44_RS12500 B9Z44_RS08505
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit B9Z44_RS12515 B9Z44_RS09455
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pco propanyl-CoA oxidase B9Z44_RS12650 B9Z44_RS14300
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase B9Z44_RS12160
prpC 2-methylcitrate synthase B9Z44_RS03160
prpD 2-methylcitrate dehydratase
prpF methylaconitate isomerase B9Z44_RS00285 B9Z44_RS12770
pta phosphate acetyltransferase B9Z44_RS09885 B9Z44_RS07290
RR42_RS28305 L-threonine:H+ symporter B9Z44_RS14795
serP1 L-threonine uptake transporter SerP1 B9Z44_RS14795
snatA L-threonine transporter snatA
sstT L-threonine:Na+ symporter SstT
tdcC L-threonine:H+ symporter TdcC
tdh L-threonine 3-dehydrogenase
tynA aminoacetone oxidase
yvgN methylglyoxal reductase (NADPH-dependent)

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