GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Sinorhizobium medicae WSM419

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 SMED_RS07965 SMED_RS21390
hisM L-lysine ABC transporter, permease component 1 (HisM) SMED_RS07975 SMED_RS00870
hisQ L-lysine ABC transporter, permease component 2 (HisQ) SMED_RS07970 SMED_RS00875
hisP L-lysine ABC transporter, ATPase component HisP SMED_RS00885 SMED_RS31560
lysDH L-lysine 6-dehydrogenase SMED_RS14660
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) SMED_RS15850 SMED_RS22390
lysN 2-aminoadipate transaminase SMED_RS15855 SMED_RS11150
hglS D-2-hydroxyglutarate synthase SMED_RS15840
ydiJ (R)-2-hydroxyglutarate dehydrogenase SMED_RS15845 SMED_RS12405
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase SMED_RS10610
amaD D-lysine oxidase SMED_RS01705
atoB acetyl-CoA C-acetyltransferase SMED_RS15645 SMED_RS25365
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit SMED_RS22665 SMED_RS21235
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase SMED_RS25860 SMED_RS03580
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit SMED_RS25350
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit SMED_RS25355
davA 5-aminovaleramidase SMED_RS12005 SMED_RS12555
davB L-lysine 2-monooxygenase
davD glutarate semialdehyde dehydrogenase SMED_RS16160 SMED_RS30660
davT 5-aminovalerate aminotransferase SMED_RS23385 SMED_RS26535
dpkA 1-piperideine-2-carboxylate reductase SMED_RS19415 SMED_RS25390
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase SMED_RS17950 SMED_RS11005
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit SMED_RS30600 SMED_RS12685
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit SMED_RS30595 SMED_RS12680
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase SMED_RS00725 SMED_RS12690
gcdG succinyl-CoA:glutarate CoA-transferase SMED_RS23360 SMED_RS28455
gcdH glutaryl-CoA dehydrogenase SMED_RS23355 SMED_RS22665
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase SMED_RS17460
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 SMED_RS19340 SMED_RS10845
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase SMED_RS23385 SMED_RS26535
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) SMED_RS20225
LHT L-lysine transporter
lysL L-lysine transporter LysL
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase SMED_RS00640 SMED_RS25335
patD 5-aminopentanal dehydrogenase SMED_RS10935 SMED_RS02820
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