GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Ochrobactrum rhizosphaerae PR17

Best path

argT, hisM, hisQ, hisP, lysDH, amaB, lysN, hglS, ydiJ

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 (28 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT CEV32_RS11040 CEV32_RS03975
hisM L-lysine ABC transporter, permease component 1 (HisM) CEV32_RS11030 CEV32_RS00780
hisQ L-lysine ABC transporter, permease component 2 (HisQ) CEV32_RS11035 CEV32_RS07450
hisP L-lysine ABC transporter, ATPase component HisP CEV32_RS07440 CEV32_RS02145
lysDH L-lysine 6-dehydrogenase CEV32_RS03965
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) CEV32_RS14575 CEV32_RS21345
lysN 2-aminoadipate transaminase CEV32_RS13905 CEV32_RS13300
hglS D-2-hydroxyglutarate synthase CEV32_RS14570
ydiJ (R)-2-hydroxyglutarate dehydrogenase CEV32_RS20770 CEV32_RS06440
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase CEV32_RS14560
amaD D-lysine oxidase CEV32_RS03980 CEV32_RS02565
atoB acetyl-CoA C-acetyltransferase CEV32_RS16630 CEV32_RS14805
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit CEV32_RS18875 CEV32_RS13060
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase CEV32_RS20935 CEV32_RS22915
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit
davA 5-aminovaleramidase CEV32_RS17160
davB L-lysine 2-monooxygenase
davD glutarate semialdehyde dehydrogenase CEV32_RS15795 CEV32_RS02105
davT 5-aminovalerate aminotransferase CEV32_RS07615 CEV32_RS20200
dpkA 1-piperideine-2-carboxylate reductase CEV32_RS02320 CEV32_RS06690
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase CEV32_RS18700 CEV32_RS07690
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit CEV32_RS17250 CEV32_RS07205
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase CEV32_RS03030 CEV32_RS17245
gcdG succinyl-CoA:glutarate CoA-transferase CEV32_RS11820 CEV32_RS07740
gcdH glutaryl-CoA dehydrogenase CEV32_RS11825 CEV32_RS18875
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
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
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase CEV32_RS07615 CEV32_RS02705
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) CEV32_RS02745
LHT L-lysine transporter
lysL L-lysine transporter LysL
lysP L-lysine:H+ symporter LysP CEV32_RS22695 CEV32_RS22015
patA cadaverine aminotransferase CEV32_RS01035 CEV32_RS20200
patD 5-aminopentanal dehydrogenase CEV32_RS02780 CEV32_RS21345
Slc7a1 L-lysine transporter Slc7a1

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