GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Mesorhizobium ciceri biovar biserrulae WSM1271

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 (30 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argT L-lysine ABC transporter, substrate-binding component ArgT MESCI_RS19705 MESCI_RS03465
hisM L-lysine ABC transporter, permease component 1 (HisM) MESCI_RS19715 MESCI_RS13050
hisQ L-lysine ABC transporter, permease component 2 (HisQ) MESCI_RS19710 MESCI_RS13055
hisP L-lysine ABC transporter, ATPase component HisP MESCI_RS33060 MESCI_RS01590
cadA lysine decarboxylase MESCI_RS09615 MESCI_RS22175
patA cadaverine aminotransferase MESCI_RS29885 MESCI_RS16850
patD 5-aminopentanal dehydrogenase MESCI_RS00735 MESCI_RS13255
davT 5-aminovalerate aminotransferase MESCI_RS00215 MESCI_RS29885
davD glutarate semialdehyde dehydrogenase MESCI_RS17265 MESCI_RS28355
gcdG succinyl-CoA:glutarate CoA-transferase MESCI_RS15670 MESCI_RS01310
gcdH glutaryl-CoA dehydrogenase MESCI_RS09970 MESCI_RS24275
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase MESCI_RS30135 MESCI_RS23380
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase MESCI_RS05330 MESCI_RS29955
atoB acetyl-CoA C-acetyltransferase MESCI_RS06630 MESCI_RS05450
Alternative steps:
alr lysine racemase MESCI_RS29690
amaA L-pipecolate oxidase MESCI_RS26230 MESCI_RS25630
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) MESCI_RS10005 MESCI_RS01365
amaD D-lysine oxidase MESCI_RS22965
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit MESCI_RS24275 MESCI_RS17130
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit
davA 5-aminovaleramidase MESCI_RS07990
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase MESCI_RS31020 MESCI_RS08720
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit MESCI_RS29155 MESCI_RS07845
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit MESCI_RS29150 MESCI_RS07850
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 MESCI_RS14310
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 MESCI_RS02110 MESCI_RS21700
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase MESCI_RS00215 MESCI_RS26490
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) MESCI_RS12230
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase MESCI_RS04400
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase MESCI_RS30990 MESCI_RS11300
lysP L-lysine:H+ symporter LysP
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase MESCI_RS25385 MESCI_RS12975

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