GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Sinorhizobium fredii NGR234

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 (32 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT NGR_RS19835 NGR_RS01715
hisM L-lysine ABC transporter, permease component 1 (HisM) NGR_RS19845 NGR_RS01705
hisQ L-lysine ABC transporter, permease component 2 (HisQ) NGR_RS19840 NGR_RS12345
hisP L-lysine ABC transporter, ATPase component HisP NGR_RS12355 NGR_RS17840
lysDH L-lysine 6-dehydrogenase NGR_RS26680
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) NGR_RS27600 NGR_RS23205
lysN 2-aminoadipate transaminase NGR_RS27605 NGR_RS01505
hglS D-2-hydroxyglutarate synthase NGR_RS27590
ydiJ (R)-2-hydroxyglutarate dehydrogenase NGR_RS01475 NGR_RS27595
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase NGR_RS21895 NGR_RS10555
amaD D-lysine oxidase NGR_RS13160 NGR_RS26220
atoB acetyl-CoA C-acetyltransferase NGR_RS27475 NGR_RS26100
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit NGR_RS05525 NGR_RS10015
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase NGR_RS15640 NGR_RS25770
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit
davA 5-aminovaleramidase NGR_RS23790 NGR_RS24455
davB L-lysine 2-monooxygenase
davD glutarate semialdehyde dehydrogenase NGR_RS27930 NGR_RS06520
davT 5-aminovalerate aminotransferase NGR_RS06525 NGR_RS12135
dpkA 1-piperideine-2-carboxylate reductase NGR_RS28210 NGR_RS24080
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase NGR_RS29675 NGR_RS12210
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit NGR_RS30350 NGR_RS07945
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit NGR_RS30345 NGR_RS24600
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase NGR_RS24175 NGR_RS12210
gcdG succinyl-CoA:glutarate CoA-transferase NGR_RS06375 NGR_RS02365
gcdH glutaryl-CoA dehydrogenase NGR_RS06370 NGR_RS05525
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase NGR_RS29175
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 NGR_RS14520 NGR_RS21970
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase NGR_RS06525 NGR_RS30440
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) NGR_RS06795
LHT L-lysine transporter
lysL L-lysine transporter LysL NGR_RS25415 NGR_RS25420
lysP L-lysine:H+ symporter LysP NGR_RS11085
patA cadaverine aminotransferase NGR_RS26550 NGR_RS12135
patD 5-aminopentanal dehydrogenase NGR_RS22050 NGR_RS26215
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 Apr 09 2024. 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