GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Tistlia consotensis USBA 355

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 (29 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT B9O00_RS08525 B9O00_RS08535
hisM L-lysine ABC transporter, permease component 1 (HisM) B9O00_RS08515 B9O00_RS25795
hisQ L-lysine ABC transporter, permease component 2 (HisQ) B9O00_RS08520 B9O00_RS25800
hisP L-lysine ABC transporter, ATPase component HisP B9O00_RS08530 B9O00_RS06665
davB L-lysine 2-monooxygenase
davA 5-aminovaleramidase B9O00_RS31615 B9O00_RS13950
davT 5-aminovalerate aminotransferase B9O00_RS06850 B9O00_RS00755
davD glutarate semialdehyde dehydrogenase B9O00_RS05420 B9O00_RS21375
gcdG succinyl-CoA:glutarate CoA-transferase B9O00_RS18960 B9O00_RS14030
gcdH glutaryl-CoA dehydrogenase B9O00_RS18005 B9O00_RS18920
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase B9O00_RS03145 B9O00_RS14075
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase B9O00_RS02065 B9O00_RS06390
atoB acetyl-CoA C-acetyltransferase B9O00_RS02255 B9O00_RS06430
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase B9O00_RS12615
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) B9O00_RS00790 B9O00_RS04475
amaD D-lysine oxidase B9O00_RS23545 B9O00_RS10565
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit B9O00_RS11550 B9O00_RS08980
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase B9O00_RS18720 B9O00_RS16780
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit B9O00_RS13585
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit B9O00_RS13580
dpkA 1-piperideine-2-carboxylate reductase B9O00_RS02510 B9O00_RS04015
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit B9O00_RS02060
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit B9O00_RS02055
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 B9O00_RS16290 B9O00_RS28920
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase B9O00_RS00610 B9O00_RS06850
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) B9O00_RS04040
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase B9O00_RS27325 B9O00_RS12295
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase B9O00_RS06850 B9O00_RS11815
patD 5-aminopentanal dehydrogenase B9O00_RS19750 B9O00_RS20310
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase B9O00_RS03905 B9O00_RS04010

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