GapMind for catabolism of small carbon sources

 

Definition of L-lysine catabolism

As rules and steps, or see full text

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.

Steps

lysP: L-lysine:H+ symporter LysP

LHT: L-lysine transporter

Slc7a1: L-lysine transporter Slc7a1

lysL: L-lysine transporter LysL

argT: L-lysine ABC transporter, substrate-binding component ArgT

hisM: L-lysine ABC transporter, permease component 1 (HisM)

hisQ: L-lysine ABC transporter, permease component 2 (HisQ)

hisP: L-lysine ABC transporter, ATPase component HisP

bgtB: L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)

atoB: acetyl-CoA C-acetyltransferase

gcdH: glutaryl-CoA dehydrogenase

ech: (S)-3-hydroxybutanoyl-CoA hydro-lyase

fadB: (S)-3-hydroxybutanoyl-CoA dehydrogenase

glaH: glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)

lhgD: L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO)

gcdG: succinyl-CoA:glutarate CoA-transferase

davT: 5-aminovalerate aminotransferase

davD: glutarate semialdehyde dehydrogenase

lysN: 2-aminoadipate transaminase

hglS: D-2-hydroxyglutarate synthase

ydiJ: (R)-2-hydroxyglutarate dehydrogenase

cadA: lysine decarboxylase

patA: cadaverine aminotransferase

patD: 5-aminopentanal dehydrogenase

davB: L-lysine 2-monooxygenase

davA: 5-aminovaleramidase

alr: lysine racemase

amaD: D-lysine oxidase

dpkA: 1-piperideine-2-carboxylate reductase

amaA: L-pipecolate oxidase

amaB: L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd)

lat: L-lysine 6-aminotransferase

lysDH: L-lysine 6-dehydrogenase

kamA: L-lysine 2,3-aminomutase

kamD: L-beta-lysine 5,6-aminomutase, alpha subunit

kamE: L-beta-lysine 5,6-aminomutase, beta subunit

kdd: 3,5-diaminohexanoate dehydrogenase

kce: (S)-5-amino-3-oxohexanoate cleavage enzyme

kal: 3-aminobutyryl-CoA deaminase

bcd: butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit

etfA: butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit

etfB: butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit

ctfA: butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit

ctfB: butanoyl-CoA:acetoacetate CoA-transferase, beta subunit

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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