GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Halomonas salina B6

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 (32 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT BN1003_RS01395 BN1003_RS11755
hisM L-lysine ABC transporter, permease component 1 (HisM) BN1003_RS05860 BN1003_RS01405
hisQ L-lysine ABC transporter, permease component 2 (HisQ) BN1003_RS05865 BN1003_RS01400
hisP L-lysine ABC transporter, ATPase component HisP BN1003_RS01390 BN1003_RS01595
davB L-lysine 2-monooxygenase
davA 5-aminovaleramidase BN1003_RS06225 BN1003_RS06495
davT 5-aminovalerate aminotransferase BN1003_RS11280 BN1003_RS05020
davD glutarate semialdehyde dehydrogenase BN1003_RS12190 BN1003_RS11285
gcdG succinyl-CoA:glutarate CoA-transferase BN1003_RS15925 BN1003_RS09100
gcdH glutaryl-CoA dehydrogenase BN1003_RS15930 BN1003_RS16630
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase BN1003_RS10785 BN1003_RS18225
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase BN1003_RS18750 BN1003_RS10780
atoB acetyl-CoA C-acetyltransferase BN1003_RS03690 BN1003_RS11730
Alternative steps:
alr lysine racemase BN1003_RS06820 BN1003_RS02495
amaA L-pipecolate oxidase BN1003_RS18025 BN1003_RS18060
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) BN1003_RS13545 BN1003_RS11285
amaD D-lysine oxidase BN1003_RS15060
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit BN1003_RS16630 BN1003_RS15950
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase BN1003_RS07715
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit BN1003_RS14040 BN1003_RS11775
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit BN1003_RS14045 BN1003_RS11770
dpkA 1-piperideine-2-carboxylate reductase BN1003_RS16460
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit BN1003_RS17380
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit BN1003_RS17385
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD) BN1003_RS05775
hglS D-2-hydroxyglutarate synthase
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase BN1003_RS19380
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 BN1003_RS04255 BN1003_RS01330
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase BN1003_RS11280 BN1003_RS05020
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) BN1003_RS05780 BN1003_RS14825
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase BN1003_RS11280 BN1003_RS05020
lysP L-lysine:H+ symporter LysP
patA cadaverine aminotransferase BN1003_RS11280 BN1003_RS11780
patD 5-aminopentanal dehydrogenase BN1003_RS11285 BN1003_RS06365
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase BN1003_RS13595 BN1003_RS18935

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