GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Methylocystis bryophila S285

Best path

tdcC, ltaE, adh, acs, gcvP, gcvT, gcvH, lpd

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 (38 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
tdcC L-threonine:H+ symporter TdcC
ltaE L-threonine aldolase B1812_RS20455 B1812_RS07220
adh acetaldehyde dehydrogenase (not acylating) B1812_RS07050 B1812_RS13395
acs acetyl-CoA synthetase, AMP-forming B1812_RS11525 B1812_RS19225
gcvP glycine cleavage system, P component (glycine decarboxylase) B1812_RS02895
gcvT glycine cleavage system, T component (tetrahydrofolate aminomethyltransferase) B1812_RS02905 B1812_RS11135
gcvH glycine cleavage system, H component (lipoyl protein) B1812_RS02900
lpd dihydrolipoyl dehydrogenase B1812_RS15590 B1812_RS17665
Alternative steps:
ackA acetate kinase B1812_RS12000
acn (2R,3S)-2-methylcitrate dehydratase B1812_RS09215
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming) B1812_RS09215
ald-dh-CoA acetaldehyde dehydrogenase, acylating
aldA lactaldehyde dehydrogenase B1812_RS13395 B1812_RS07050
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) B1812_RS04380 B1812_RS12645
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) B1812_RS04360 B1812_RS12645
D-LDH D-lactate dehydrogenase B1812_RS11125 B1812_RS02130
dddA 3-hydroxypropionate dehydrogenase B1812_RS03215
DVU3032 L-lactate dehydrogenase, LutC-like component
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components
epi methylmalonyl-CoA epimerase B1812_RS01105
glcD D-lactate dehydrogenase, FAD-linked subunit 1 (GlcD) B1812_RS02130 B1812_RS11125
glcE D-lactate dehydrogenase, FAD-linked subunit 2 (GlcE) B1812_RS02125 B1812_RS11125
glcF D-lactate dehydrogenase, FeS subunit GlcF B1812_RS02120
gloA glyoxylase I B1812_RS06600 B1812_RS11480
gloB hydroxyacylglutathione hydrolase (glyoxalase II) B1812_RS17335 B1812_RS04175
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 B1812_RS05255 B1812_RS00705
iolA malonate semialdehyde dehydrogenase (CoA-acylating) B1812_RS16250 B1812_RS10880
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase) B1812_RS09095 B1812_RS20610
L-LDH L-lactate dehydrogenase B1812_RS07210 B1812_RS20390
lctB electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), small subunit B1812_RS07855
lctC electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), large subunit B1812_RS07850 B1812_RS04150
lctD D-lactate dehydrogenase (NAD+, ferredoxin), lactate dehydrogenase component B1812_RS02130 B1812_RS11125
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
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 B1812_RS11420 B1812_RS17195
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit B1812_RS11420 B1812_RS17195
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components B1812_RS11420 B1812_RS17195
pccA propionyl-CoA carboxylase, alpha subunit B1812_RS15355 B1812_RS16300
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit B1812_RS15355 B1812_RS04040
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit B1812_RS15355
pccB propionyl-CoA carboxylase, beta subunit B1812_RS10760 B1812_RS16290
pco propanyl-CoA oxidase
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase
prpC 2-methylcitrate synthase B1812_RS12625
prpD 2-methylcitrate dehydratase
prpF methylaconitate isomerase
pta phosphate acetyltransferase B1812_RS05165 B1812_RS11995
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
tdh L-threonine 3-dehydrogenase B1812_RS09090
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 Apr 09 2024. 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