GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Limnohabitans parvus II-B4

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) B9Z37_RS11950
braD L-alanine/L-serine/L-threonine ABC transporter, permease component 1 (BraD/NatD) B9Z37_RS09270 B9Z37_RS08650
braE L-alanine/L-serine/L-threonine ABC transporter, permease component 2 (BraE/NatC) B9Z37_RS09275 B9Z37_RS01745
braF L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 1 (BraF/NatA) B9Z37_RS09280 B9Z37_RS08660
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) B9Z37_RS09285 B9Z37_RS10195
tdcB L-threonine dehydratase B9Z37_RS12805
tdcE 2-ketobutyrate formate-lyase
pccA propionyl-CoA carboxylase, alpha subunit B9Z37_RS02070 B9Z37_RS05375
pccB propionyl-CoA carboxylase, beta subunit B9Z37_RS02075 B9Z37_RS05385
epi methylmalonyl-CoA epimerase B9Z37_RS02065
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit B9Z37_RS02085 B9Z37_RS12570
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit B9Z37_RS02085
Alternative steps:
ackA acetate kinase B9Z37_RS14075
acn (2R,3S)-2-methylcitrate dehydratase B9Z37_RS09750
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
acs acetyl-CoA synthetase, AMP-forming B9Z37_RS01260 B9Z37_RS02375
adh acetaldehyde dehydrogenase (not acylating) B9Z37_RS05925 B9Z37_RS11445
ald-dh-CoA acetaldehyde dehydrogenase, acylating
aldA lactaldehyde dehydrogenase B9Z37_RS05925 B9Z37_RS00715
D-LDH D-lactate dehydrogenase B9Z37_RS06970 B9Z37_RS11240
dddA 3-hydroxypropionate dehydrogenase B9Z37_RS06545 B9Z37_RS07390
DVU3032 L-lactate dehydrogenase, LutC-like component
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components
gcvH glycine cleavage system, H component (lipoyl protein) B9Z37_RS11350
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) B9Z37_RS06030 B9Z37_RS06970
glcE D-lactate dehydrogenase, FAD-linked subunit 2 (GlcE) B9Z37_RS06615 B9Z37_RS06970
glcF D-lactate dehydrogenase, FeS subunit GlcF B9Z37_RS06610
gloA glyoxylase I B9Z37_RS02710 B9Z37_RS03525
gloB hydroxyacylglutathione hydrolase (glyoxalase II) B9Z37_RS02270 B9Z37_RS06200
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 B9Z37_RS08455 B9Z37_RS08460
iolA malonate semialdehyde dehydrogenase (CoA-acylating) B9Z37_RS06540 B9Z37_RS06135
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase)
L-LDH L-lactate dehydrogenase B9Z37_RS09455 B9Z37_RS12655
lctB electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), small subunit
lctC electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), large subunit B9Z37_RS10105
lctD D-lactate dehydrogenase (NAD+, ferredoxin), lactate dehydrogenase component B9Z37_RS06970 B9Z37_RS06030
lctO L-lactate oxidase or 2-monooxygenase B9Z37_RS01195 B9Z37_RS09455
lldE L-lactate dehydrogenase, LldE subunit
lldF L-lactate dehydrogenase, LldF subunit
lldG L-lactate dehydrogenase, LldG subunit
lpd dihydrolipoyl dehydrogenase B9Z37_RS00425 B9Z37_RS12150
ltaE L-threonine aldolase B9Z37_RS05650 B9Z37_RS01540
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 B9Z37_RS02085 B9Z37_RS12570
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit B9Z37_RS02070 B9Z37_RS04785
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pco propanyl-CoA oxidase B9Z37_RS02770
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase B9Z37_RS00890
prpC 2-methylcitrate synthase B9Z37_RS09700
prpD 2-methylcitrate dehydratase
prpF methylaconitate isomerase B9Z37_RS10710
pta phosphate acetyltransferase B9Z37_RS07440
RR42_RS28305 L-threonine:H+ symporter
serP1 L-threonine uptake transporter SerP1
snatA L-threonine transporter snatA B9Z37_RS06530
sstT L-threonine:Na+ symporter SstT
tdcC L-threonine:H+ symporter TdcC
tdh L-threonine 3-dehydrogenase B9Z37_RS00160 B9Z37_RS02605
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.

Links

Downloads

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:

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