GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Pseudomonas baetica a390

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 (32 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT C0J26_RS08830 C0J26_RS01690
hisM L-lysine ABC transporter, permease component 1 (HisM) C0J26_RS08820 C0J26_RS01680
hisQ L-lysine ABC transporter, permease component 2 (HisQ) C0J26_RS08825 C0J26_RS01685
hisP L-lysine ABC transporter, ATPase component HisP C0J26_RS01695 C0J26_RS08810
davB L-lysine 2-monooxygenase C0J26_RS02705
davA 5-aminovaleramidase C0J26_RS02700 C0J26_RS21695
davT 5-aminovalerate aminotransferase C0J26_RS01030 C0J26_RS25540
davD glutarate semialdehyde dehydrogenase C0J26_RS01025 C0J26_RS12950
gcdG succinyl-CoA:glutarate CoA-transferase C0J26_RS00750 C0J26_RS06235
gcdH glutaryl-CoA dehydrogenase C0J26_RS00745 C0J26_RS16985
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase C0J26_RS15240 C0J26_RS25285
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase C0J26_RS25285 C0J26_RS22935
atoB acetyl-CoA C-acetyltransferase C0J26_RS15230 C0J26_RS16155
Alternative steps:
alr lysine racemase C0J26_RS27790 C0J26_RS30220
amaA L-pipecolate oxidase C0J26_RS14050 C0J26_RS15890
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) C0J26_RS01025 C0J26_RS05085
amaD D-lysine oxidase
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit C0J26_RS15235 C0J26_RS15245
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase C0J26_RS12010 C0J26_RS03165
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit C0J26_RS15385 C0J26_RS16145
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit C0J26_RS16150 C0J26_RS15380
dpkA 1-piperideine-2-carboxylate reductase C0J26_RS23155
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit C0J26_RS26420
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit C0J26_RS26425
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase C0J26_RS11165
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 C0J26_RS18100
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase C0J26_RS01030 C0J26_RS25540
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO)
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL C0J26_RS20810 C0J26_RS20815
lysN 2-aminoadipate transaminase C0J26_RS01030 C0J26_RS19195
lysP L-lysine:H+ symporter LysP C0J26_RS21710 C0J26_RS01700
patA cadaverine aminotransferase C0J26_RS22150 C0J26_RS25540
patD 5-aminopentanal dehydrogenase C0J26_RS18005 C0J26_RS27190
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase C0J26_RS12625 C0J26_RS29350

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