GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Herbaspirillum aquaticum IEH 4430

Best path

lysP, cadA, patA, patD, 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 (31 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
lysP L-lysine:H+ symporter LysP
cadA lysine decarboxylase CEJ45_RS08975 CEJ45_RS09870
patA cadaverine aminotransferase CEJ45_RS11820 CEJ45_RS12790
patD 5-aminopentanal dehydrogenase CEJ45_RS11615 CEJ45_RS01340
davT 5-aminovalerate aminotransferase CEJ45_RS11820 CEJ45_RS14475
davD glutarate semialdehyde dehydrogenase CEJ45_RS11845 CEJ45_RS11615
gcdG succinyl-CoA:glutarate CoA-transferase CEJ45_RS11495 CEJ45_RS17765
gcdH glutaryl-CoA dehydrogenase CEJ45_RS11500 CEJ45_RS12595
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase CEJ45_RS16530 CEJ45_RS06410
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase CEJ45_RS14455 CEJ45_RS11470
atoB acetyl-CoA C-acetyltransferase CEJ45_RS14415 CEJ45_RS09425
Alternative steps:
alr lysine racemase CEJ45_RS14095
amaA L-pipecolate oxidase CEJ45_RS11340
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) CEJ45_RS08610 CEJ45_RS13135
amaD D-lysine oxidase CEJ45_RS23455
argT L-lysine ABC transporter, substrate-binding component ArgT CEJ45_RS03560 CEJ45_RS10635
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit CEJ45_RS06405 CEJ45_RS12595
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit CEJ45_RS12845 CEJ45_RS16020
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit CEJ45_RS12850 CEJ45_RS16025
davA 5-aminovaleramidase CEJ45_RS15210
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase CEJ45_RS22975 CEJ45_RS07350
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit CEJ45_RS19625
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit CEJ45_RS19630
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
hisM L-lysine ABC transporter, permease component 1 (HisM) CEJ45_RS04235 CEJ45_RS07290
hisP L-lysine ABC transporter, ATPase component HisP CEJ45_RS21940 CEJ45_RS14125
hisQ L-lysine ABC transporter, permease component 2 (HisQ) CEJ45_RS11350 CEJ45_RS04235
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 CEJ45_RS09015
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase CEJ45_RS11820 CEJ45_RS09555
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) CEJ45_RS10670
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase CEJ45_RS14630
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase CEJ45_RS11820 CEJ45_RS05715
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase CEJ45_RS08600 CEJ45_RS15240

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