GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Thioalkalivibrio denitrificans ALJD

Best path

snatA, ltaE, adh, ackA, pta, 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 (39 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
snatA L-threonine transporter snatA B1C78_RS15540
ltaE L-threonine aldolase B1C78_RS07180
adh acetaldehyde dehydrogenase (not acylating) B1C78_RS12570 B1C78_RS10500
ackA acetate kinase B1C78_RS16585 B1C78_RS09870
pta phosphate acetyltransferase B1C78_RS02400 B1C78_RS03420
gcvP glycine cleavage system, P component (glycine decarboxylase) B1C78_RS08130 B1C78_RS08120
gcvT glycine cleavage system, T component (tetrahydrofolate aminomethyltransferase) B1C78_RS08140 B1C78_RS04885
gcvH glycine cleavage system, H component (lipoyl protein) B1C78_RS08135 B1C78_RS14855
lpd dihydrolipoyl dehydrogenase B1C78_RS09695 B1C78_RS11485
Alternative steps:
acn (2R,3S)-2-methylcitrate dehydratase
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
acs acetyl-CoA synthetase, AMP-forming B1C78_RS08305 B1C78_RS13700
ald-dh-CoA acetaldehyde dehydrogenase, acylating B1C78_RS09900
aldA lactaldehyde dehydrogenase B1C78_RS10500 B1C78_RS12570
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) B1C78_RS02765 B1C78_RS04795
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) B1C78_RS02765 B1C78_RS10420
D-LDH D-lactate dehydrogenase B1C78_RS03900 B1C78_RS04705
dddA 3-hydroxypropionate dehydrogenase
DVU3032 L-lactate dehydrogenase, LutC-like component B1C78_RS11860
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components B1C78_RS11855
epi methylmalonyl-CoA epimerase
glcD D-lactate dehydrogenase, FAD-linked subunit 1 (GlcD) B1C78_RS03960 B1C78_RS04705
glcE D-lactate dehydrogenase, FAD-linked subunit 2 (GlcE) B1C78_RS07155 B1C78_RS04705
glcF D-lactate dehydrogenase, FeS subunit GlcF B1C78_RS07150 B1C78_RS01470
gloA glyoxylase I B1C78_RS11175 B1C78_RS01355
gloB hydroxyacylglutathione hydrolase (glyoxalase II) B1C78_RS03490 B1C78_RS07880
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
iolA malonate semialdehyde dehydrogenase (CoA-acylating) B1C78_RS10500 B1C78_RS12570
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase) B1C78_RS02340
L-LDH L-lactate dehydrogenase B1C78_RS01115 B1C78_RS03320
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 B1C78_RS04705 B1C78_RS03960
lctO L-lactate oxidase or 2-monooxygenase
lldE L-lactate dehydrogenase, LldE subunit B1C78_RS11850
lldF L-lactate dehydrogenase, LldF subunit B1C78_RS11855
lldG L-lactate dehydrogenase, LldG subunit
lutA L-lactate dehydrogenase, LutA subunit B1C78_RS11850
lutB L-lactate dehydrogenase, LutB subunit B1C78_RS11855
lutC L-lactate dehydrogenase, LutC subunit B1C78_RS11860
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit B1C78_RS09190
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components
pccA propionyl-CoA carboxylase, alpha subunit B1C78_RS11965 B1C78_RS01095
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit B1C78_RS01095 B1C78_RS11965
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit B1C78_RS01100
pccB propionyl-CoA carboxylase, beta subunit
pco propanyl-CoA oxidase
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase B1C78_RS10515 B1C78_RS13710
prpC 2-methylcitrate synthase B1C78_RS13715 B1C78_RS02405
prpD 2-methylcitrate dehydratase B1C78_RS13720
prpF methylaconitate isomerase
RR42_RS28305 L-threonine:H+ symporter
serP1 L-threonine uptake transporter SerP1
sstT L-threonine:Na+ symporter SstT
tdcB L-threonine dehydratase B1C78_RS08215 B1C78_RS04160
tdcC L-threonine:H+ symporter TdcC
tdcE 2-ketobutyrate formate-lyase
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