GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Saccharomonospora marina XMU15

Best path

lysP, 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 (27 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
lysP L-lysine:H+ symporter LysP
cadA lysine decarboxylase SACMADRAFT_RS04570 SACMADRAFT_RS10825
patA cadaverine aminotransferase SACMADRAFT_RS17095 SACMADRAFT_RS11300
patD 5-aminopentanal dehydrogenase SACMADRAFT_RS08720 SACMADRAFT_RS26445
davT 5-aminovalerate aminotransferase SACMADRAFT_RS21055 SACMADRAFT_RS17095
davD glutarate semialdehyde dehydrogenase SACMADRAFT_RS21050 SACMADRAFT_RS08720
gcdG succinyl-CoA:glutarate CoA-transferase SACMADRAFT_RS17670 SACMADRAFT_RS11800
gcdH glutaryl-CoA dehydrogenase SACMADRAFT_RS06025 SACMADRAFT_RS21150
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase SACMADRAFT_RS19140 SACMADRAFT_RS21080
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase SACMADRAFT_RS27015 SACMADRAFT_RS12380
atoB acetyl-CoA C-acetyltransferase SACMADRAFT_RS19295 SACMADRAFT_RS10145
Alternative steps:
alr lysine racemase SACMADRAFT_RS03680 SACMADRAFT_RS15230
amaA L-pipecolate oxidase
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) SACMADRAFT_RS26445 SACMADRAFT_RS21050
amaD D-lysine oxidase SACMADRAFT_RS09640
argT L-lysine ABC transporter, substrate-binding component ArgT SACMADRAFT_RS27825
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit SACMADRAFT_RS04405 SACMADRAFT_RS21150
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit SACMADRAFT_RS19575
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit SACMADRAFT_RS19570
davA 5-aminovaleramidase
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit SACMADRAFT_RS18950 SACMADRAFT_RS09425
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit SACMADRAFT_RS18955
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
hisM L-lysine ABC transporter, permease component 1 (HisM) SACMADRAFT_RS15020 SACMADRAFT_RS20060
hisP L-lysine ABC transporter, ATPase component HisP SACMADRAFT_RS18450 SACMADRAFT_RS27815
hisQ L-lysine ABC transporter, permease component 2 (HisQ) SACMADRAFT_RS15020 SACMADRAFT_RS20060
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase SACMADRAFT_RS14015
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 SACMADRAFT_RS21055 SACMADRAFT_RS08915
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) SACMADRAFT_RS01685
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase SACMADRAFT_RS03235 SACMADRAFT_RS21055
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase SACMADRAFT_RS05330 SACMADRAFT_RS21065

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