GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Halomonas smyrnensis AAD6

Best path

argT, hisM, hisQ, hisP, 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 (33 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT UYS_RS0211370 UYS_RS0212205
hisM L-lysine ABC transporter, permease component 1 (HisM) UYS_RS0212200 UYS_RS0211380
hisQ L-lysine ABC transporter, permease component 2 (HisQ) UYS_RS0212195 UYS_RS0211375
hisP L-lysine ABC transporter, ATPase component HisP UYS_RS0211365 UYS_RS0203445
cadA lysine decarboxylase UYS_RS0210605 UYS_RS0214945
patA cadaverine aminotransferase UYS_RS0212955 UYS_RS0208645
patD 5-aminopentanal dehydrogenase UYS_RS0205480 UYS_RS0212960
davT 5-aminovalerate aminotransferase UYS_RS0212955 UYS_RS0203385
davD glutarate semialdehyde dehydrogenase UYS_RS0205685 UYS_RS0206440
gcdG succinyl-CoA:glutarate CoA-transferase UYS_RS0206560 UYS_RS0210215
gcdH glutaryl-CoA dehydrogenase UYS_RS0206555 UYS_RS0209860
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase UYS_RS0213615 UYS_RS0210210
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase UYS_RS0202585 UYS_RS0213620
atoB acetyl-CoA C-acetyltransferase UYS_RS0202795 UYS_RS0214820
Alternative steps:
alr lysine racemase UYS_RS0215800 UYS_RS0203980
amaA L-pipecolate oxidase UYS_RS0203420
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) UYS_RS0203400 UYS_RS0212960
amaD D-lysine oxidase UYS_RS0208215
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit UYS_RS0215605 UYS_RS0209860
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit UYS_RS0207290
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit UYS_RS0207295
davA 5-aminovaleramidase UYS_RS0211760 UYS_RS0204845
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase UYS_RS0203415 UYS_RS0211480
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit UYS_RS0204660
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit UYS_RS0204665
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD) UYS_RS0212280
hglS D-2-hydroxyglutarate synthase UYS_RS0203375
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase UYS_RS0213825
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 UYS_RS0211160
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase UYS_RS0212955 UYS_RS0203385
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) UYS_RS0212275 UYS_RS0214375
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase UYS_RS0203385 UYS_RS0212955
lysP L-lysine:H+ symporter LysP
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase UYS_RS0201975 UYS_RS0203380

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