GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Halomonas titanicae BH1

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 HALTITAN_RS15020
davB L-lysine 2-monooxygenase
davA 5-aminovaleramidase HALTITAN_RS00275 HALTITAN_RS04660
davT 5-aminovalerate aminotransferase HALTITAN_RS00620 HALTITAN_RS07740
davD glutarate semialdehyde dehydrogenase HALTITAN_RS06075 HALTITAN_RS00625
gcdG succinyl-CoA:glutarate CoA-transferase HALTITAN_RS07755 HALTITAN_RS23045
gcdH glutaryl-CoA dehydrogenase HALTITAN_RS07760 HALTITAN_RS05155
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase HALTITAN_RS11900 HALTITAN_RS16865
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase HALTITAN_RS23950 HALTITAN_RS11895
atoB acetyl-CoA C-acetyltransferase HALTITAN_RS18010 HALTITAN_RS18730
Alternative steps:
alr lysine racemase HALTITAN_RS04230 HALTITAN_RS12505
amaA L-pipecolate oxidase
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) HALTITAN_RS06075 HALTITAN_RS00625
amaD D-lysine oxidase HALTITAN_RS07100
argT L-lysine ABC transporter, substrate-binding component ArgT HALTITAN_RS11445 HALTITAN_RS15235
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit HALTITAN_RS23060 HALTITAN_RS05155
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase HALTITAN_RS23150
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit HALTITAN_RS07015
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit HALTITAN_RS07020
dpkA 1-piperideine-2-carboxylate reductase HALTITAN_RS07445 HALTITAN_RS13995
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit HALTITAN_RS23340 HALTITAN_RS16840
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit HALTITAN_RS04840 HALTITAN_RS16835
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase HALTITAN_RS03755
hisM L-lysine ABC transporter, permease component 1 (HisM) HALTITAN_RS15240 HALTITAN_RS11435
hisP L-lysine ABC transporter, ATPase component HisP HALTITAN_RS11450 HALTITAN_RS02850
hisQ L-lysine ABC transporter, permease component 2 (HisQ) HALTITAN_RS15245 HALTITAN_RS11440
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase HALTITAN_RS16125
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 HALTITAN_RS03470 HALTITAN_RS15745
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase HALTITAN_RS01040 HALTITAN_RS07740
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO)
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase HALTITAN_RS00620 HALTITAN_RS07740
patA cadaverine aminotransferase HALTITAN_RS00620 HALTITAN_RS07740
patD 5-aminopentanal dehydrogenase HALTITAN_RS23055 HALTITAN_RS05610
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase HALTITAN_RS13950 HALTITAN_RS02510

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