GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Pseudomonas taeanensis MS-3

Best path

argT, hisM, hisQ, hisP, lysDH, amaB, lysN, hglS, ydiJ

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 (33 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT TMS3_RS04805 TMS3_RS12735
hisM L-lysine ABC transporter, permease component 1 (HisM) TMS3_RS04795 TMS3_RS12725
hisQ L-lysine ABC transporter, permease component 2 (HisQ) TMS3_RS04800 TMS3_RS12730
hisP L-lysine ABC transporter, ATPase component HisP TMS3_RS04810 TMS3_RS12740
lysDH L-lysine 6-dehydrogenase TMS3_RS12710
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) TMS3_RS12820 TMS3_RS02055
lysN 2-aminoadipate transaminase TMS3_RS12810 TMS3_RS22180
hglS D-2-hydroxyglutarate synthase TMS3_RS12800
ydiJ (R)-2-hydroxyglutarate dehydrogenase TMS3_RS01750 TMS3_RS19250
Alternative steps:
alr lysine racemase TMS3_RS00035 TMS3_RS05880
amaA L-pipecolate oxidase TMS3_RS07885 TMS3_RS16830
amaD D-lysine oxidase TMS3_RS01605
atoB acetyl-CoA C-acetyltransferase TMS3_RS07820 TMS3_RS15420
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit TMS3_RS15300 TMS3_RS15395
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase TMS3_RS12705 TMS3_RS07880
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit TMS3_RS15430
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit TMS3_RS15425
davA 5-aminovaleramidase TMS3_RS13415 TMS3_RS09705
davB L-lysine 2-monooxygenase
davD glutarate semialdehyde dehydrogenase TMS3_RS02055 TMS3_RS10945
davT 5-aminovalerate aminotransferase TMS3_RS12810 TMS3_RS11185
dpkA 1-piperideine-2-carboxylate reductase TMS3_RS08405 TMS3_RS01630
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase TMS3_RS14965 TMS3_RS21560
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit TMS3_RS08875 TMS3_RS21890
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit TMS3_RS08870 TMS3_RS21885
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase TMS3_RS21560 TMS3_RS22410
gcdG succinyl-CoA:glutarate CoA-transferase TMS3_RS02090 TMS3_RS09880
gcdH glutaryl-CoA dehydrogenase TMS3_RS02095 TMS3_RS15395
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD) TMS3_RS10930
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 TMS3_RS00610
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase TMS3_RS08980 TMS3_RS12810
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) TMS3_RS10935
LHT L-lysine transporter
lysL L-lysine transporter LysL
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase TMS3_RS11185 TMS3_RS03905
patD 5-aminopentanal dehydrogenase TMS3_RS09905 TMS3_RS00885
Slc7a1 L-lysine transporter Slc7a1

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