GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Actinokineospora bangkokensis 44EHW

Best path

lysP, kamA, kamD, kamE, kdd, kce, kal, bcd, etfA, etfB, ctfA, ctfB, 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 (36 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
lysP L-lysine:H+ symporter LysP BJP25_RS17955
kamA L-lysine 2,3-aminomutase BJP25_RS10610
kamD L-beta-lysine 5,6-aminomutase, alpha subunit BJP25_RS10625
kamE L-beta-lysine 5,6-aminomutase, beta subunit BJP25_RS10630
kdd 3,5-diaminohexanoate dehydrogenase BJP25_RS10615
kce (S)-5-amino-3-oxohexanoate cleavage enzyme BJP25_RS25710
kal 3-aminobutyryl-CoA deaminase BJP25_RS10635
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit BJP25_RS23200 BJP25_RS15595
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit BJP25_RS21095
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit BJP25_RS21100
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit BJP25_RS10040 BJP25_RS12280
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit BJP25_RS10035 BJP25_RS12285
atoB acetyl-CoA C-acetyltransferase BJP25_RS21275 BJP25_RS14530
Alternative steps:
alr lysine racemase BJP25_RS24050
amaA L-pipecolate oxidase
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) BJP25_RS10080 BJP25_RS03115
amaD D-lysine oxidase
argT L-lysine ABC transporter, substrate-binding component ArgT BJP25_RS26350
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase BJP25_RS05460 BJP25_RS03155
davA 5-aminovaleramidase BJP25_RS01320 BJP25_RS01325
davB L-lysine 2-monooxygenase
davD glutarate semialdehyde dehydrogenase BJP25_RS23515 BJP25_RS30850
davT 5-aminovalerate aminotransferase BJP25_RS03110 BJP25_RS14785
dpkA 1-piperideine-2-carboxylate reductase BJP25_RS12715
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase BJP25_RS21155 BJP25_RS29180
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase BJP25_RS15590 BJP25_RS21355
gcdG succinyl-CoA:glutarate CoA-transferase BJP25_RS00640
gcdH glutaryl-CoA dehydrogenase BJP25_RS05505 BJP25_RS22655
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase BJP25_RS10075
hisM L-lysine ABC transporter, permease component 1 (HisM) BJP25_RS13430 BJP25_RS26345
hisP L-lysine ABC transporter, ATPase component HisP BJP25_RS02395 BJP25_RS26340
hisQ L-lysine ABC transporter, permease component 2 (HisQ) BJP25_RS13430 BJP25_RS26345
lat L-lysine 6-aminotransferase BJP25_RS14785 BJP25_RS03110
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) BJP25_RS12870
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase BJP25_RS00055 BJP25_RS26845
patA cadaverine aminotransferase BJP25_RS19925 BJP25_RS03070
patD 5-aminopentanal dehydrogenase BJP25_RS30850 BJP25_RS29000
Slc7a1 L-lysine transporter Slc7a1 BJP25_RS23025
ydiJ (R)-2-hydroxyglutarate dehydrogenase BJP25_RS08050 BJP25_RS08800

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