GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Brevibacterium jeotgali SJ5-8

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 (39 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
tdcC L-threonine:H+ symporter TdcC
ltaE L-threonine aldolase BJEO58_RS10740 BJEO58_RS00050
adh acetaldehyde dehydrogenase (not acylating) BJEO58_RS09005 BJEO58_RS03430
acs acetyl-CoA synthetase, AMP-forming BJEO58_RS01030 BJEO58_RS03345
gcvP glycine cleavage system, P component (glycine decarboxylase) BJEO58_RS05735
gcvT glycine cleavage system, T component (tetrahydrofolate aminomethyltransferase) BJEO58_RS05740 BJEO58_RS01645
gcvH glycine cleavage system, H component (lipoyl protein) BJEO58_RS10720 BJEO58_RS05745
lpd dihydrolipoyl dehydrogenase BJEO58_RS13395 BJEO58_RS13775
Alternative steps:
ackA acetate kinase
acn (2R,3S)-2-methylcitrate dehydratase BJEO58_RS11005
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming) BJEO58_RS11005
ald-dh-CoA acetaldehyde dehydrogenase, acylating
aldA lactaldehyde dehydrogenase BJEO58_RS09005 BJEO58_RS12670
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) BJEO58_RS05330 BJEO58_RS04205
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) BJEO58_RS03195 BJEO58_RS05330
D-LDH D-lactate dehydrogenase BJEO58_RS04575 BJEO58_RS11240
dddA 3-hydroxypropionate dehydrogenase BJEO58_RS08510
DVU3032 L-lactate dehydrogenase, LutC-like component
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components BJEO58_RS00830
epi methylmalonyl-CoA epimerase
glcD D-lactate dehydrogenase, FAD-linked subunit 1 (GlcD) BJEO58_RS04575 BJEO58_RS11240
glcE D-lactate dehydrogenase, FAD-linked subunit 2 (GlcE) BJEO58_RS04575 BJEO58_RS11240
glcF D-lactate dehydrogenase, FeS subunit GlcF
gloA glyoxylase I
gloB hydroxyacylglutathione hydrolase (glyoxalase II) BJEO58_RS08265 BJEO58_RS02875
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 BJEO58_RS08900 BJEO58_RS03580
iolA malonate semialdehyde dehydrogenase (CoA-acylating) BJEO58_RS07395 BJEO58_RS05335
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase)
L-LDH L-lactate dehydrogenase BJEO58_RS06785 BJEO58_RS02060
lctB electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), small subunit
lctC electron-transfer flavoprotein for D-lactate dehydrogenase (NAD+, ferredoxin), large subunit BJEO58_RS08125
lctD D-lactate dehydrogenase (NAD+, ferredoxin), lactate dehydrogenase component BJEO58_RS01305 BJEO58_RS04575
lctO L-lactate oxidase or 2-monooxygenase
lldE L-lactate dehydrogenase, LldE subunit BJEO58_RS00825
lldF L-lactate dehydrogenase, LldF subunit BJEO58_RS00830
lldG L-lactate dehydrogenase, LldG subunit
lutA L-lactate dehydrogenase, LutA subunit BJEO58_RS00825
lutB L-lactate dehydrogenase, LutB subunit BJEO58_RS00830
lutC L-lactate dehydrogenase, LutC subunit BJEO58_RS00835
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 BJEO58_RS00855 BJEO58_RS09820
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit BJEO58_RS14660 BJEO58_RS09820
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pccB propionyl-CoA carboxylase, beta subunit BJEO58_RS10090 BJEO58_RS00860
pco propanyl-CoA oxidase BJEO58_RS02315 BJEO58_RS04410
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase BJEO58_RS05660 BJEO58_RS00620
prpC 2-methylcitrate synthase BJEO58_RS00615 BJEO58_RS12875
prpD 2-methylcitrate dehydratase BJEO58_RS00625
prpF methylaconitate isomerase
pta phosphate acetyltransferase
RR42_RS28305 L-threonine:H+ symporter BJEO58_RS06510
serP1 L-threonine uptake transporter SerP1
snatA L-threonine transporter snatA
sstT L-threonine:Na+ symporter SstT
tdcB L-threonine dehydratase BJEO58_RS01510 BJEO58_RS06800
tdcE 2-ketobutyrate formate-lyase
tdh L-threonine 3-dehydrogenase BJEO58_RS06500 BJEO58_RS03565
tynA aminoacetone oxidase
yvgN methylglyoxal reductase (NADPH-dependent) BJEO58_RS10490

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