GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Skermanella stibiiresistens SB22

Best path

lysP, 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 (31 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
lysP L-lysine:H+ symporter LysP
davB L-lysine 2-monooxygenase
davA 5-aminovaleramidase N825_RS04475 N825_RS19545
davT 5-aminovalerate aminotransferase N825_RS22125 N825_RS18655
davD glutarate semialdehyde dehydrogenase N825_RS24260 N825_RS30470
gcdG succinyl-CoA:glutarate CoA-transferase N825_RS02640 N825_RS10970
gcdH glutaryl-CoA dehydrogenase N825_RS18065 N825_RS14805
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase N825_RS27875 N825_RS00490
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase N825_RS07770 N825_RS29290
atoB acetyl-CoA C-acetyltransferase N825_RS19860 N825_RS25015
Alternative steps:
alr lysine racemase N825_RS02440
amaA L-pipecolate oxidase N825_RS26640
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) N825_RS12870 N825_RS24260
amaD D-lysine oxidase N825_RS07155
argT L-lysine ABC transporter, substrate-binding component ArgT N825_RS00140 N825_RS02255
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit N825_RS25025 N825_RS18045
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase N825_RS28390 N825_RS01715
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit N825_RS12900 N825_RS01845
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit N825_RS12895 N825_RS01850
dpkA 1-piperideine-2-carboxylate reductase N825_RS26645 N825_RS22720
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit N825_RS16370 N825_RS29295
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit N825_RS16365 N825_RS29300
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
hisM L-lysine ABC transporter, permease component 1 (HisM) N825_RS00130 N825_RS30510
hisP L-lysine ABC transporter, ATPase component HisP N825_RS00145 N825_RS06450
hisQ L-lysine ABC transporter, permease component 2 (HisQ) N825_RS00135 N825_RS30510
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase N825_RS00280
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 N825_RS31860 N825_RS25125
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase N825_RS25205 N825_RS17305
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) N825_RS09610
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase N825_RS34200 N825_RS08875
patA cadaverine aminotransferase N825_RS18655 N825_RS22125
patD 5-aminopentanal dehydrogenase N825_RS01910 N825_RS24260
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase N825_RS33930 N825_RS28240

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