GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Bacillus coahuilensis m4-4

Best path

tdcC, tdh, tynA, yvgN, aldA, L-LDH

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 (29 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
tdcC L-threonine:H+ symporter TdcC
tdh L-threonine 3-dehydrogenase M44_RS01620
tynA aminoacetone oxidase
yvgN methylglyoxal reductase (NADPH-dependent) M44_RS14710 M44_RS17615
aldA lactaldehyde dehydrogenase M44_RS04450 M44_RS06330
L-LDH L-lactate dehydrogenase M44_RS18035 M44_RS13235
Alternative steps:
ackA acetate kinase M44_RS13085 M44_RS11025
acn (2R,3S)-2-methylcitrate dehydratase
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
acs acetyl-CoA synthetase, AMP-forming M44_RS13040 M44_RS04675
adh acetaldehyde dehydrogenase (not acylating) M44_RS14855 M44_RS16260
ald-dh-CoA acetaldehyde dehydrogenase, acylating
braC L-alanine/L-serine/L-threonine ABC transporter, substrate binding protein (BraC/NatB)
braD L-alanine/L-serine/L-threonine ABC transporter, permease component 1 (BraD/NatD)
braE L-alanine/L-serine/L-threonine ABC transporter, permease component 2 (BraE/NatC)
braF L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 1 (BraF/NatA) M44_RS14780 M44_RS17840
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) M44_RS14670 M44_RS17840
D-LDH D-lactate dehydrogenase M44_RS16615
dddA 3-hydroxypropionate dehydrogenase
DVU3032 L-lactate dehydrogenase, LutC-like component
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components
epi methylmalonyl-CoA epimerase M44_RS10170 M44_RS18640
gcvH glycine cleavage system, H component (lipoyl protein) M44_RS16435
gcvP glycine cleavage system, P component (glycine decarboxylase) M44_RS10750
gcvT glycine cleavage system, T component (tetrahydrofolate aminomethyltransferase)
glcD D-lactate dehydrogenase, FAD-linked subunit 1 (GlcD)
glcE D-lactate dehydrogenase, FAD-linked subunit 2 (GlcE)
glcF D-lactate dehydrogenase, FeS subunit GlcF
gloA glyoxylase I M44_RS04900 M44_RS10170
gloB hydroxyacylglutathione hydrolase (glyoxalase II) M44_RS10660
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 M44_RS04440 M44_RS12670
iolA malonate semialdehyde dehydrogenase (CoA-acylating) M44_RS14855 M44_RS04450
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase) M44_RS01615 M44_RS03890
lctB electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), small subunit
lctC electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), large subunit
lctD D-lactate dehydrogenase (NAD+, ferredoxin), lactate dehydrogenase component
lctO L-lactate oxidase or 2-monooxygenase
lldE L-lactate dehydrogenase, LldE subunit
lldF L-lactate dehydrogenase, LldF subunit
lldG L-lactate dehydrogenase, LldG subunit
lpd dihydrolipoyl dehydrogenase M44_RS04525 M44_RS01905
ltaE L-threonine aldolase M44_RS17185
lutA L-lactate dehydrogenase, LutA subunit
lutB L-lactate dehydrogenase, LutB subunit
lutC L-lactate dehydrogenase, LutC subunit
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit M44_RS22490 M44_RS17015
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit M44_RS22490
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components M44_RS22490 M44_RS17015
pccA propionyl-CoA carboxylase, alpha subunit M44_RS10915
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit M44_RS10915
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pccB propionyl-CoA carboxylase, beta subunit
pco propanyl-CoA oxidase M44_RS16995 M44_RS17000
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase M44_RS02855
prpC 2-methylcitrate synthase
prpD 2-methylcitrate dehydratase
prpF methylaconitate isomerase
pta phosphate acetyltransferase M44_RS17465
RR42_RS28305 L-threonine:H+ symporter
serP1 L-threonine uptake transporter SerP1
snatA L-threonine transporter snatA
sstT L-threonine:Na+ symporter SstT
tdcB L-threonine dehydratase
tdcE 2-ketobutyrate formate-lyase M44_RS09035

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