GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Phyllobacterium brassicacearum STM 196

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 (30 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT CU102_RS05655 CU102_RS07740
hisM L-lysine ABC transporter, permease component 1 (HisM) CU102_RS05665 CU102_RS07750
hisQ L-lysine ABC transporter, permease component 2 (HisQ) CU102_RS05660 CU102_RS07745
hisP L-lysine ABC transporter, ATPase component HisP CU102_RS27085 CU102_RS16040
lysDH L-lysine 6-dehydrogenase CU102_RS22040
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) CU102_RS17790 CU102_RS00695
lysN 2-aminoadipate transaminase CU102_RS03165 CU102_RS07230
hglS D-2-hydroxyglutarate synthase CU102_RS17795
ydiJ (R)-2-hydroxyglutarate dehydrogenase CU102_RS01195 CU102_RS07670
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase CU102_RS17805
amaD D-lysine oxidase CU102_RS14455
atoB acetyl-CoA C-acetyltransferase CU102_RS21705 CU102_RS10795
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit CU102_RS06015 CU102_RS00185
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase CU102_RS15560 CU102_RS29060
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit CU102_RS22230
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit CU102_RS22225
davA 5-aminovaleramidase CU102_RS20165 CU102_RS14070
davB L-lysine 2-monooxygenase
davD glutarate semialdehyde dehydrogenase CU102_RS19905 CU102_RS05845
davT 5-aminovalerate aminotransferase CU102_RS14190 CU102_RS07845
dpkA 1-piperideine-2-carboxylate reductase CU102_RS02815 CU102_RS20590
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase CU102_RS13700 CU102_RS18480
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit CU102_RS10360
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit CU102_RS10365
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase CU102_RS14135 CU102_RS10355
gcdG succinyl-CoA:glutarate CoA-transferase CU102_RS06915 CU102_RS11790
gcdH glutaryl-CoA dehydrogenase CU102_RS01740 CU102_RS00185
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 CU102_RS18575 CU102_RS07810
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase CU102_RS00900 CU102_RS20920
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO)
LHT L-lysine transporter
lysL L-lysine transporter LysL
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase CU102_RS07845 CU102_RS14190
patD 5-aminopentanal dehydrogenase CU102_RS11730 CU102_RS00695
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