GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Hoeflea phototrophica DFL-43

Best path

argT, hisM, hisQ, hisP, davB, davA, davT, davD, gcdG, gcdH, ech, fadB, atoB

Rules

Overview: Lysine degradation in GapMind is based on many metacyc pathways (link), including L-lysine degradation I via cadaverine (link), pathway IV via lysine monooxygenase (link), pathway V via D-lysine (link), pathway VI via lysine 6-aminotransferase (link), pathway VIII via lysine 6-dehydrogenase (link), and fermentation to acetate and butanoate (link). Pathway X (link) is similar to pathway I (with cadaverine and glutarate as intermediates), but glutarate is consumed via glutaryl-CoA (as in pathway IV); it does not introduce any new steps. Pathways II (L-pipecolate pathway) and III (via N6-acetyllysine) and VII (via 6-amino-2-oxohexanoate) and IX (similar to pathway IV) and XI (via saccharopine) are not thought to occur in prokaryotes and are not included in GapMind.

44 steps (26 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT HPDFL43_RS05610
hisM L-lysine ABC transporter, permease component 1 (HisM) HPDFL43_RS05620 HPDFL43_RS20460
hisQ L-lysine ABC transporter, permease component 2 (HisQ) HPDFL43_RS05615 HPDFL43_RS20460
hisP L-lysine ABC transporter, ATPase component HisP HPDFL43_RS11450 HPDFL43_RS05605
davB L-lysine 2-monooxygenase
davA 5-aminovaleramidase HPDFL43_RS11215 HPDFL43_RS19260
davT 5-aminovalerate aminotransferase HPDFL43_RS02770 HPDFL43_RS11280
davD glutarate semialdehyde dehydrogenase HPDFL43_RS05720 HPDFL43_RS19090
gcdG succinyl-CoA:glutarate CoA-transferase HPDFL43_RS16075
gcdH glutaryl-CoA dehydrogenase HPDFL43_RS14295 HPDFL43_RS13350
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase HPDFL43_RS01490 HPDFL43_RS02870
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase HPDFL43_RS13380 HPDFL43_RS02870
atoB acetyl-CoA C-acetyltransferase HPDFL43_RS19835 HPDFL43_RS15010
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase HPDFL43_RS13675
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) HPDFL43_RS14915 HPDFL43_RS05720
amaD D-lysine oxidase HPDFL43_RS18600
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit HPDFL43_RS11100 HPDFL43_RS15500
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase HPDFL43_RS14455 HPDFL43_RS18535
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit
dpkA 1-piperideine-2-carboxylate reductase HPDFL43_RS19660 HPDFL43_RS14225
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit HPDFL43_RS19405
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit HPDFL43_RS19400
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase
kamD L-beta-lysine 5,6-aminomutase, alpha subunit
kamE L-beta-lysine 5,6-aminomutase, beta subunit
kce (S)-5-amino-3-oxohexanoate cleavage enzyme HPDFL43_RS05630
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase HPDFL43_RS10830 HPDFL43_RS17020
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO)
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase HPDFL43_RS16345 HPDFL43_RS07675
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase HPDFL43_RS11280 HPDFL43_RS02770
patD 5-aminopentanal dehydrogenase HPDFL43_RS05720 HPDFL43_RS14915
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase HPDFL43_RS06340 HPDFL43_RS14745

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