GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Rhodococcus qingshengii djl-6-2

Best path

bgtB, 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 (32 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB) C1M55_RS30350 C1M55_RS21980
hisP L-lysine ABC transporter, ATPase component HisP C1M55_RS13925 C1M55_RS16555
davB L-lysine 2-monooxygenase C1M55_RS03275
davA 5-aminovaleramidase C1M55_RS03270 C1M55_RS20210
davT 5-aminovalerate aminotransferase C1M55_RS28045 C1M55_RS03290
davD glutarate semialdehyde dehydrogenase C1M55_RS22335 C1M55_RS03295
gcdG succinyl-CoA:glutarate CoA-transferase C1M55_RS24685 C1M55_RS30270
gcdH glutaryl-CoA dehydrogenase C1M55_RS24690 C1M55_RS09530
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase C1M55_RS19610 C1M55_RS12340
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase C1M55_RS07980 C1M55_RS25285
atoB acetyl-CoA C-acetyltransferase C1M55_RS28700 C1M55_RS07210
Alternative steps:
alr lysine racemase C1M55_RS20010 C1M55_RS09635
amaA L-pipecolate oxidase C1M55_RS07385
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) C1M55_RS10720 C1M55_RS28050
amaD D-lysine oxidase
argT L-lysine ABC transporter, substrate-binding component ArgT C1M55_RS21980
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit C1M55_RS25280 C1M55_RS09270
cadA lysine decarboxylase C1M55_RS20580
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit C1M55_RS26645 C1M55_RS06025
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit C1M55_RS26640 C1M55_RS09290
dpkA 1-piperideine-2-carboxylate reductase
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit C1M55_RS12390
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit C1M55_RS12385
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase C1M55_RS10725
hisM L-lysine ABC transporter, permease component 1 (HisM) C1M55_RS21980 C1M55_RS30350
hisQ L-lysine ABC transporter, permease component 2 (HisQ) C1M55_RS21980 C1M55_RS07370
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 C1M55_RS02105
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase C1M55_RS10735 C1M55_RS03290
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 C1M55_RS01535 C1M55_RS03290
lysP L-lysine:H+ symporter LysP C1M55_RS01060 C1M55_RS07700
patA cadaverine aminotransferase C1M55_RS16390 C1M55_RS03290
patD 5-aminopentanal dehydrogenase C1M55_RS22220 C1M55_RS28575
Slc7a1 L-lysine transporter Slc7a1 C1M55_RS10990 C1M55_RS12490
ydiJ (R)-2-hydroxyglutarate dehydrogenase C1M55_RS29255 C1M55_RS20295

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