GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Psychromonas ingrahamii 37

Best path

sstT, 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 (41 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
sstT L-threonine:Na+ symporter SstT PING_RS02650
ltaE L-threonine aldolase PING_RS11815 PING_RS07590
adh acetaldehyde dehydrogenase (not acylating) PING_RS13070 PING_RS17105
ackA acetate kinase PING_RS14235 PING_RS17085
pta phosphate acetyltransferase PING_RS17090
gcvP glycine cleavage system, P component (glycine decarboxylase) PING_RS14085
gcvT glycine cleavage system, T component (tetrahydrofolate aminomethyltransferase) PING_RS14070
gcvH glycine cleavage system, H component (lipoyl protein) PING_RS14080
lpd dihydrolipoyl dehydrogenase PING_RS15075 PING_RS14345
Alternative steps:
acn (2R,3S)-2-methylcitrate dehydratase PING_RS09730 PING_RS14940
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming) PING_RS09730 PING_RS10955
acs acetyl-CoA synthetase, AMP-forming PING_RS16055 PING_RS18580
ald-dh-CoA acetaldehyde dehydrogenase, acylating PING_RS17105
aldA lactaldehyde dehydrogenase PING_RS13070 PING_RS10720
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) PING_RS14900 PING_RS15400
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) PING_RS15405 PING_RS14900
D-LDH D-lactate dehydrogenase PING_RS07480 PING_RS00525
dddA 3-hydroxypropionate dehydrogenase PING_RS10725
DVU3032 L-lactate dehydrogenase, LutC-like component
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components PING_RS07490 PING_RS08860
epi methylmalonyl-CoA epimerase
glcD D-lactate dehydrogenase, FAD-linked subunit 1 (GlcD) PING_RS07480
glcE D-lactate dehydrogenase, FAD-linked subunit 2 (GlcE)
glcF D-lactate dehydrogenase, FeS subunit GlcF
gloA glyoxylase I PING_RS00905 PING_RS08580
gloB hydroxyacylglutathione hydrolase (glyoxalase II) PING_RS02620 PING_RS01135
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 PING_RS03450 PING_RS03455
iolA malonate semialdehyde dehydrogenase (CoA-acylating) PING_RS12385 PING_RS10720
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase) PING_RS09655 PING_RS09995
L-LDH L-lactate dehydrogenase
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 PING_RS08855 PING_RS07495
lldF L-lactate dehydrogenase, LldF subunit PING_RS08860 PING_RS07490
lldG L-lactate dehydrogenase, LldG subunit
lutA L-lactate dehydrogenase, LutA subunit PING_RS07495 PING_RS08855
lutB L-lactate dehydrogenase, LutB subunit PING_RS07490 PING_RS08860
lutC L-lactate dehydrogenase, LutC subunit PING_RS07485
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components
pccA propionyl-CoA carboxylase, alpha subunit PING_RS14630
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit PING_RS14630
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit PING_RS17415
pccB propionyl-CoA carboxylase, beta subunit
pco propanyl-CoA oxidase
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase PING_RS09740
prpC 2-methylcitrate synthase PING_RS09735 PING_RS13510
prpD 2-methylcitrate dehydratase PING_RS08215
prpF methylaconitate isomerase PING_RS09725
RR42_RS28305 L-threonine:H+ symporter
serP1 L-threonine uptake transporter SerP1
snatA L-threonine transporter snatA PING_RS08115 PING_RS07345
tdcB L-threonine dehydratase PING_RS17230
tdcC L-threonine:H+ symporter TdcC
tdcE 2-ketobutyrate formate-lyase PING_RS17065
tdh L-threonine 3-dehydrogenase PING_RS09660 PING_RS17105
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