GapMind for catabolism of small carbon sources

 

L-threonine catabolism in Chlorobium phaeobacteroides BS1

Best path

snatA, 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 (31 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
snatA L-threonine transporter snatA Cphamn1_0155
ltaE L-threonine aldolase Cphamn1_0630
adh acetaldehyde dehydrogenase (not acylating) Cphamn1_2121 Cphamn1_2056
acs acetyl-CoA synthetase, AMP-forming Cphamn1_0550 Cphamn1_1176
gcvP glycine cleavage system, P component (glycine decarboxylase) Cphamn1_0176 Cphamn1_0592
gcvT glycine cleavage system, T component (tetrahydrofolate aminomethyltransferase) Cphamn1_2020
gcvH glycine cleavage system, H component (lipoyl protein) Cphamn1_0591
lpd dihydrolipoyl dehydrogenase Cphamn1_1045 Cphamn1_1481
Alternative steps:
ackA acetate kinase Cphamn1_2557
acn (2R,3S)-2-methylcitrate dehydratase Cphamn1_1817 Cphamn1_2466
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming) Cphamn1_2466
ald-dh-CoA acetaldehyde dehydrogenase, acylating
aldA lactaldehyde dehydrogenase Cphamn1_2009 Cphamn1_2056
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) Cphamn1_0698
braF L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 1 (BraF/NatA) Cphamn1_0699 Cphamn1_2170
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) Cphamn1_0700 Cphamn1_2170
D-LDH D-lactate dehydrogenase Cphamn1_1806 Cphamn1_1569
dddA 3-hydroxypropionate dehydrogenase
DVU3032 L-lactate dehydrogenase, LutC-like component
DVU3033 L-lactate dehydrogenase, fused LutA/LutB components
epi methylmalonyl-CoA epimerase Cphamn1_1175
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
gloB hydroxyacylglutathione hydrolase (glyoxalase II) Cphamn1_0282
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 Cphamn1_2111 Cphamn1_2077
iolA malonate semialdehyde dehydrogenase (CoA-acylating)
kbl glycine C-acetyltransferase (2-amino-3-ketobutyrate CoA-ligase) Cphamn1_2203 Cphamn1_2457
L-LDH L-lactate dehydrogenase Cphamn1_0832
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
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 Cphamn1_1173
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit Cphamn1_1173 Cphamn1_2093
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components Cphamn1_1173
pccA propionyl-CoA carboxylase, alpha subunit Cphamn1_0321
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit Cphamn1_0321
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit Cphamn1_1200
pccB propionyl-CoA carboxylase, beta subunit
pco propanyl-CoA oxidase Cphamn1_0670
phtA L-threonine uptake permease PhtA
prpB 2-methylisocitrate lyase
prpC 2-methylcitrate synthase Cphamn1_2068
prpD 2-methylcitrate dehydratase
prpF methylaconitate isomerase
pta phosphate acetyltransferase
RR42_RS28305 L-threonine:H+ symporter
serP1 L-threonine uptake transporter SerP1
sstT L-threonine:Na+ symporter SstT
tdcB L-threonine dehydratase
tdcC L-threonine:H+ symporter TdcC
tdcE 2-ketobutyrate formate-lyase
tdh L-threonine 3-dehydrogenase Cphamn1_1084
tynA aminoacetone oxidase
yvgN methylglyoxal reductase (NADPH-dependent) Cphamn1_0788

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