GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Lutibaculum baratangense AMV1

Best path

argT, hisM, hisQ, hisP, 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 (30 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT N177_RS02605 N177_RS07675
hisM L-lysine ABC transporter, permease component 1 (HisM) N177_RS02595 N177_RS07665
hisQ L-lysine ABC transporter, permease component 2 (HisQ) N177_RS02600 N177_RS07670
hisP L-lysine ABC transporter, ATPase component HisP N177_RS07680 N177_RS16485
cadA lysine decarboxylase N177_RS19565 N177_RS01880
patA cadaverine aminotransferase N177_RS00515 N177_RS19680
patD 5-aminopentanal dehydrogenase N177_RS08305 N177_RS12830
davT 5-aminovalerate aminotransferase N177_RS00515 N177_RS19680
davD glutarate semialdehyde dehydrogenase N177_RS19425 N177_RS00820
gcdG succinyl-CoA:glutarate CoA-transferase N177_RS03095 N177_RS14855
gcdH glutaryl-CoA dehydrogenase N177_RS18745 N177_RS14805
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase N177_RS05770 N177_RS14645
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase N177_RS04545 N177_RS13530
atoB acetyl-CoA C-acetyltransferase N177_RS12075 N177_RS02410
Alternative steps:
alr lysine racemase N177_RS16265 N177_RS17835
amaA L-pipecolate oxidase N177_RS00345 N177_RS13505
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) N177_RS05465 N177_RS08305
amaD D-lysine oxidase N177_RS20170 N177_RS00430
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit N177_RS14635 N177_RS14805
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit N177_RS16545
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit N177_RS16550
davA 5-aminovaleramidase N177_RS02245 N177_RS04695
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase N177_RS08105 N177_RS11375
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit N177_RS12695
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit N177_RS12690
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
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 N177_RS17045 N177_RS19675
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase N177_RS00515 N177_RS01755
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) N177_RS12845
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase N177_RS03375 N177_RS07690
lysP L-lysine:H+ symporter LysP
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase N177_RS10090 N177_RS01155

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