GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Bradyrhizobium diazoefficiens USDA110

Best path

lysL, cadA, patA, patD, 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 (31 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
lysL L-lysine transporter LysL BJA_RS37140 BJA_RS37070
cadA lysine decarboxylase BJA_RS18780 BJA_RS39380
patA cadaverine aminotransferase BJA_RS05560 BJA_RS14150
patD 5-aminopentanal dehydrogenase BJA_RS14720 BJA_RS32015
davT 5-aminovalerate aminotransferase BJA_RS05560 BJA_RS14430
davD glutarate semialdehyde dehydrogenase BJA_RS04085 BJA_RS38580
gcdG succinyl-CoA:glutarate CoA-transferase BJA_RS27565 BJA_RS03715
gcdH glutaryl-CoA dehydrogenase BJA_RS12935 BJA_RS22060
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase BJA_RS15040 BJA_RS32235
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase BJA_RS31520 BJA_RS39695
atoB acetyl-CoA C-acetyltransferase BJA_RS18410 BJA_RS39620
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase BJA_RS10865 BJA_RS34590
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) BJA_RS04085 BJA_RS29725
amaD D-lysine oxidase BJA_RS21405 BJA_RS32605
argT L-lysine ABC transporter, substrate-binding component ArgT BJA_RS05750 BJA_RS10850
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit BJA_RS19610 BJA_RS22060
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit BJA_RS17175 BJA_RS35965
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit BJA_RS17170 BJA_RS35960
davA 5-aminovaleramidase BJA_RS16515 BJA_RS04925
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase BJA_RS14465 BJA_RS38450
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit BJA_RS08930 BJA_RS07015
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit BJA_RS10005 BJA_RS07010
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
hisM L-lysine ABC transporter, permease component 1 (HisM) BJA_RS22285 BJA_RS16415
hisP L-lysine ABC transporter, ATPase component HisP BJA_RS15365 BJA_RS22215
hisQ L-lysine ABC transporter, permease component 2 (HisQ) BJA_RS36530 BJA_RS10855
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase BJA_RS21865
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 BJA_RS27575 BJA_RS27560
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase BJA_RS20530 BJA_RS19485
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) BJA_RS36035
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysN 2-aminoadipate transaminase BJA_RS17925 BJA_RS37615
lysP L-lysine:H+ symporter LysP
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase BJA_RS12655 BJA_RS31525

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