GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Rhizobium freirei PRF 81

Best path

argT, hisM, hisQ, hisP, lysDH, amaB, lysN, hglS, ydiJ

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 RHSP_RS03670 RHSP_RS00535
hisM L-lysine ABC transporter, permease component 1 (HisM) RHSP_RS03680 RHSP_RS22960
hisQ L-lysine ABC transporter, permease component 2 (HisQ) RHSP_RS03675 RHSP_RS22965
hisP L-lysine ABC transporter, ATPase component HisP RHSP_RS08130 RHSP_RS00540
lysDH L-lysine 6-dehydrogenase RHSP_RS09400
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) RHSP_RS09385 RHSP_RS26425
lysN 2-aminoadipate transaminase RHSP_RS09390 RHSP_RS11085
hglS D-2-hydroxyglutarate synthase RHSP_RS09380
ydiJ (R)-2-hydroxyglutarate dehydrogenase RHSP_RS09395 RHSP_RS04905
Alternative steps:
alr lysine racemase RHSP_RS20500
amaA L-pipecolate oxidase RHSP_RS18170 RHSP_RS26430
amaD D-lysine oxidase RHSP_RS04250 RHSP_RS16255
atoB acetyl-CoA C-acetyltransferase RHSP_RS28350 RHSP_RS31340
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit RHSP_RS25890 RHSP_RS19445
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase RHSP_RS13425 RHSP_RS27255
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit RHSP_RS31330
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit RHSP_RS31335
davA 5-aminovaleramidase RHSP_RS00580 RHSP_RS14170
davB L-lysine 2-monooxygenase
davD glutarate semialdehyde dehydrogenase RHSP_RS06225 RHSP_RS23545
davT 5-aminovalerate aminotransferase RHSP_RS29535 RHSP_RS18005
dpkA 1-piperideine-2-carboxylate reductase RHSP_RS05430 RHSP_RS26420
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase RHSP_RS02715 RHSP_RS30920
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit RHSP_RS26745 RHSP_RS07120
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit RHSP_RS26750 RHSP_RS32195
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase RHSP_RS12325 RHSP_RS06890
gcdG succinyl-CoA:glutarate CoA-transferase RHSP_RS10450 RHSP_RS31460
gcdH glutaryl-CoA dehydrogenase RHSP_RS12310 RHSP_RS31465
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase RHSP_RS28195 RHSP_RS31215
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 RHSP_RS07720 RHSP_RS06675
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase RHSP_RS29535 RHSP_RS18005
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO)
LHT L-lysine transporter
lysL L-lysine transporter LysL
lysP L-lysine:H+ symporter LysP RHSP_RS26460
patA cadaverine aminotransferase RHSP_RS30730 RHSP_RS29535
patD 5-aminopentanal dehydrogenase RHSP_RS13620 RHSP_RS16250
Slc7a1 L-lysine transporter Slc7a1

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