GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

Best path

argT, hisM, hisQ, 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 (29 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT HTA01S_RS08135 HTA01S_RS07510
hisM L-lysine ABC transporter, permease component 1 (HisM) HTA01S_RS08125 HTA01S_RS07500
hisQ L-lysine ABC transporter, permease component 2 (HisQ) HTA01S_RS07505 HTA01S_RS08130
hisP L-lysine ABC transporter, ATPase component HisP HTA01S_RS08115 HTA01S_RS18545
davB L-lysine 2-monooxygenase HTA01S_RS05415
davA 5-aminovaleramidase HTA01S_RS05420 HTA01S_RS07340
davT 5-aminovalerate aminotransferase HTA01S_RS18580 HTA01S_RS10480
davD glutarate semialdehyde dehydrogenase HTA01S_RS19000 HTA01S_RS02155
gcdG succinyl-CoA:glutarate CoA-transferase HTA01S_RS20285 HTA01S_RS18575
gcdH glutaryl-CoA dehydrogenase HTA01S_RS14830 HTA01S_RS11035
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase HTA01S_RS03890 HTA01S_RS13945
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase HTA01S_RS04710 HTA01S_RS19105
atoB acetyl-CoA C-acetyltransferase HTA01S_RS02090 HTA01S_RS06660
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase HTA01S_RS06180
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) HTA01S_RS06175 HTA01S_RS16360
amaD D-lysine oxidase HTA01S_RS02995
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit HTA01S_RS11060 HTA01S_RS11035
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase HTA01S_RS07920 HTA01S_RS07355
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit HTA01S_RS02180
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit HTA01S_RS02175
dpkA 1-piperideine-2-carboxylate reductase HTA01S_RS20635 HTA01S_RS13410
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit HTA01S_RS15335 HTA01S_RS01940
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit HTA01S_RS15330 HTA01S_RS01945
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
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
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase HTA01S_RS19080 HTA01S_RS18580
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) HTA01S_RS06830
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase HTA01S_RS18580 HTA01S_RS10480
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase HTA01S_RS17425 HTA01S_RS10480
patD 5-aminopentanal dehydrogenase HTA01S_RS06375 HTA01S_RS02155
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase HTA01S_RS02835

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