GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Amycolatopsis xylanica CPCC 202699

Best path

lysP, davB, davA, 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
lysP L-lysine:H+ symporter LysP BLV57_RS32970 BLV57_RS20100
davB L-lysine 2-monooxygenase BLV57_RS29700
davA 5-aminovaleramidase BLV57_RS29695 BLV57_RS39840
davT 5-aminovalerate aminotransferase BLV57_RS39900 BLV57_RS16625
davD glutarate semialdehyde dehydrogenase BLV57_RS16620 BLV57_RS05155
gcdG succinyl-CoA:glutarate CoA-transferase BLV57_RS16500 BLV57_RS02345
gcdH glutaryl-CoA dehydrogenase BLV57_RS34500 BLV57_RS20510
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase BLV57_RS35310 BLV57_RS23875
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase BLV57_RS10700 BLV57_RS16705
atoB acetyl-CoA C-acetyltransferase BLV57_RS25480 BLV57_RS23280
Alternative steps:
alr lysine racemase BLV57_RS27945
amaA L-pipecolate oxidase BLV57_RS17150
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) BLV57_RS16620 BLV57_RS23815
amaD D-lysine oxidase BLV57_RS24125
argT L-lysine ABC transporter, substrate-binding component ArgT BLV57_RS11175
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit BLV57_RS16765 BLV57_RS29200
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
cadA lysine decarboxylase BLV57_RS29420 BLV57_RS15290
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit BLV57_RS07065
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit BLV57_RS07060
dpkA 1-piperideine-2-carboxylate reductase BLV57_RS38920 BLV57_RS37180
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit BLV57_RS35545 BLV57_RS11490
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit BLV57_RS35540
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
hisM L-lysine ABC transporter, permease component 1 (HisM) BLV57_RS11980 BLV57_RS31000
hisP L-lysine ABC transporter, ATPase component HisP BLV57_RS33970 BLV57_RS11975
hisQ L-lysine ABC transporter, permease component 2 (HisQ) BLV57_RS11980 BLV57_RS11165
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase BLV57_RS05880
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 BLV57_RS16625 BLV57_RS39900
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) BLV57_RS41050
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase
lysL L-lysine transporter LysL
lysN 2-aminoadipate transaminase BLV57_RS39900 BLV57_RS16625
patA cadaverine aminotransferase BLV57_RS37845 BLV57_RS24140
patD 5-aminopentanal dehydrogenase BLV57_RS10935 BLV57_RS23815
Slc7a1 L-lysine transporter Slc7a1 BLV57_RS17200 BLV57_RS22090
ydiJ (R)-2-hydroxyglutarate dehydrogenase

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