GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Azospirillum humicireducens SgZ-5

Best path

bgtB, 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 (32 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
hisP L-lysine ABC transporter, ATPase component HisP A6A40_RS12685 A6A40_RS06760
cadA lysine decarboxylase A6A40_RS02045 A6A40_RS20000
patA cadaverine aminotransferase A6A40_RS27690 A6A40_RS01095
patD 5-aminopentanal dehydrogenase A6A40_RS29725 A6A40_RS13560
davT 5-aminovalerate aminotransferase A6A40_RS27690 A6A40_RS01095
davD glutarate semialdehyde dehydrogenase A6A40_RS27695 A6A40_RS18505
gcdG succinyl-CoA:glutarate CoA-transferase A6A40_RS27685 A6A40_RS02650
gcdH glutaryl-CoA dehydrogenase A6A40_RS26290 A6A40_RS19620
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase A6A40_RS14715 A6A40_RS26600
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase A6A40_RS13055 A6A40_RS28460
atoB acetyl-CoA C-acetyltransferase A6A40_RS09435 A6A40_RS28855
Alternative steps:
alr lysine racemase A6A40_RS19315
amaA L-pipecolate oxidase A6A40_RS12755 A6A40_RS22570
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) A6A40_RS28350 A6A40_RS13560
amaD D-lysine oxidase A6A40_RS01285
argT L-lysine ABC transporter, substrate-binding component ArgT A6A40_RS12680 A6A40_RS15265
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit A6A40_RS19630 A6A40_RS19620
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit A6A40_RS26060 A6A40_RS22045
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit A6A40_RS22040 A6A40_RS26065
davA 5-aminovaleramidase A6A40_RS05810
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase A6A40_RS26910 A6A40_RS11110
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit A6A40_RS02200 A6A40_RS14045
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit A6A40_RS02195 A6A40_RS00350
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase A6A40_RS12765
hisM L-lysine ABC transporter, permease component 1 (HisM) A6A40_RS12670 A6A40_RS29325
hisQ L-lysine ABC transporter, permease component 2 (HisQ) A6A40_RS12675 A6A40_RS29325
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase A6A40_RS00285
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 A6A40_RS27690 A6A40_RS11435
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) A6A40_RS09680
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase A6A40_RS14205
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase A6A40_RS27690 A6A40_RS08785
lysP L-lysine:H+ symporter LysP
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase A6A40_RS09870 A6A40_RS17375

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