GapMind for catabolism of small carbon sources

 

L-serine catabolism in Roseateles aquatilis CCUG 48205

Best path

Ac3H11_2396, Ac3H11_1695, Ac3H11_1694, Ac3H11_1693, Ac3H11_1692, sdaB

Rules

Overview: L-serine degradation in GapMind is based on the MetaCyc pathway (link)

19 steps (12 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
Ac3H11_2396 L-tyrosine ABC transporter, substrate-binding component component CDN99_RS06805
Ac3H11_1695 L-tyrosine ABC transporter, permease component 1 CDN99_RS12005 CDN99_RS22250
Ac3H11_1694 L-tyrosine ABC transporter, permease component 2 CDN99_RS12000 CDN99_RS04350
Ac3H11_1693 L-tyrosine ABC transporter, ATPase component 1 CDN99_RS11995 CDN99_RS22255
Ac3H11_1692 L-tyrosine ABC transporter, ATPase component 2 CDN99_RS11990 CDN99_RS22260
sdaB L-serine ammonia-lyase CDN99_RS06850 CDN99_RS00345
Alternative steps:
AAP1 L-serine transporter AAP1
braC L-alanine/L-serine/L-threonine ABC transporter, substrate binding protein (BraC/NatB) CDN99_RS06805
braD L-alanine/L-serine/L-threonine ABC transporter, permease component 1 (BraD/NatD) CDN99_RS12005 CDN99_RS22250
braE L-alanine/L-serine/L-threonine ABC transporter, permease component 2 (BraE/NatC) CDN99_RS12000 CDN99_RS22255
braF L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 1 (BraF/NatA) CDN99_RS11995 CDN99_RS04360
braG L-alanine/L-serine/L-threonine ABC transporter, ATP-binding component 2 (BraG/NatE) CDN99_RS22260 CDN99_RS11990
dlsT L-serine transporter DlsT
sdaC L-serine transporter:H+ symporter sdaC
sdhA FeS-containing L-serine dehydratase, alpha subunit CDN99_RS06850
sdhB FeS-containing L-serine dehydratase, beta subunit
serP L-serine permease SerP
snatA L-serine transporter
sstT L-serine:Na+ symporter SstT

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