GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Marinobacter psychrophilus 20041

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 (30 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT ABA45_RS15530 ABA45_RS07440
hisM L-lysine ABC transporter, permease component 1 (HisM) ABA45_RS15540 ABA45_RS10555
hisQ L-lysine ABC transporter, permease component 2 (HisQ) ABA45_RS15535 ABA45_RS14715
hisP L-lysine ABC transporter, ATPase component HisP ABA45_RS09175 ABA45_RS15525
davB L-lysine 2-monooxygenase
davA 5-aminovaleramidase ABA45_RS09545
davT 5-aminovalerate aminotransferase ABA45_RS01835 ABA45_RS00035
davD glutarate semialdehyde dehydrogenase ABA45_RS10590 ABA45_RS01840
gcdG succinyl-CoA:glutarate CoA-transferase ABA45_RS01500 ABA45_RS01715
gcdH glutaryl-CoA dehydrogenase ABA45_RS01505 ABA45_RS15055
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase ABA45_RS15595 ABA45_RS12250
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase ABA45_RS08125 ABA45_RS15035
atoB acetyl-CoA C-acetyltransferase ABA45_RS15265 ABA45_RS12120
Alternative steps:
alr lysine racemase ABA45_RS03050
amaA L-pipecolate oxidase
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) ABA45_RS05640 ABA45_RS01840
amaD D-lysine oxidase ABA45_RS01735
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit ABA45_RS12140 ABA45_RS12255
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase ABA45_RS01920 ABA45_RS00350
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit ABA45_RS05665 ABA45_RS07425
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit ABA45_RS05660 ABA45_RS07430
dpkA 1-piperideine-2-carboxylate reductase ABA45_RS07470 ABA45_RS01625
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit ABA45_RS09730
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit ABA45_RS09735
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase ABA45_RS08665
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase ABA45_RS13075
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
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase ABA45_RS00035 ABA45_RS01835
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) ABA45_RS12965
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase ABA45_RS07220 ABA45_RS01835
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase ABA45_RS07420 ABA45_RS00035
patD 5-aminopentanal dehydrogenase ABA45_RS14435 ABA45_RS06205
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase ABA45_RS13155 ABA45_RS01725

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