asp-kinase, asd, dapA, dapB, DAPtransferase, dapF, lysA
Overview: Lysine biosynthesis in GapMind is based on MetaCyc pathways L-lysine biosynthesis I via diaminopimelate (DAP) and succinylated intermediates (link), II with DAP and acetylated intermediates (link), III with DAP and no blocking group (link), V via 2-aminoadipate and LysW carrier protein (link), and VI with DAP aminotransferase (link). Most of these pathways involve tetrahydrodipicolinate and meso-diaminopimelate, with variations in how the amino group is introduced. Pathway V instead involves L-2-aminoadipate and LysW-attached intermediates. Lysine biosynthesis IV (link), via 2-aminoadipate and saccharopine, is only reported to occur in eukaryotes and is not described here.
Or see definitions of steps
Step | Description | Best candidate | 2nd candidate |
---|---|---|---|
asp-kinase | aspartate kinase | HM1_RS08725 | HM1_RS10585 |
asd | aspartate semi-aldehyde dehydrogenase | HM1_RS10580 | |
dapA | 4-hydroxy-tetrahydrodipicolinate synthase | HM1_RS10590 | |
dapB | 4-hydroxy-tetrahydrodipicolinate reductase | HM1_RS10565 | |
DAPtransferase | L,L-diaminopimelate aminotransferase | HM1_RS04450 | HM1_RS10910 |
dapF | diaminopimelate epimerase | HM1_RS09585 | |
lysA | diaminopimelate decarboxylase | HM1_RS08460 | |
Alternative steps: | |||
dapC | N-succinyldiaminopimelate aminotransferase | HM1_RS09160 | HM1_RS05100 |
dapD | tetrahydrodipicolinate succinylase | ||
dapE | succinyl-diaminopimelate desuccinylase | ||
dapH | tetrahydrodipicolinate acetyltransferase | HM1_RS06160 | HM1_RS05640 |
dapL | N-acetyl-diaminopimelate deacetylase | ||
dapX | acetyl-diaminopimelate aminotransferase | HM1_RS11430 | HM1_RS02935 |
ddh | meso-diaminopimelate D-dehydrogenase | ||
hcs | homocitrate synthase | HM1_RS13635 | HM1_RS05075 |
hicdh | homo-isocitrate dehydrogenase | HM1_RS06690 | HM1_RS06905 |
lysJ | [LysW]-2-aminoadipate semialdehyde transaminase | HM1_RS08735 | HM1_RS06545 |
lysK | [LysW]-lysine hydrolase | ||
lysN | 2-aminoadipate:2-oxoglutarate aminotransferase | HM1_RS02935 | HM1_RS11430 |
lysT | homoaconitase large subunit | HM1_RS06895 | HM1_RS00460 |
lysU | homoaconitase small subunit | HM1_RS06900 | HM1_RS00460 |
lysW | 2-aminoadipate/glutamate carrier protein | ||
lysX | 2-aminoadipate-LysW ligase | ||
lysY | [LysW]-2-aminoadipate 6-phosphate reductase | HM1_RS06530 | |
lysZ | [LysW]-2-aminoadipate 6-kinase | HM1_RS06540 |
Confidence: high confidence medium confidence low confidence
? – known gap: despite the lack of a good candidate for this step, this organism (or a related organism) performs the pathway
This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.
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:
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