GapMind for catabolism of small carbon sources

 

2'-deoxyinosine catabolism in Rhizobium leguminosarum bv. trifolii WSM1325

Best path

H281DRAFT_01115, H281DRAFT_01114, H281DRAFT_01113, H281DRAFT_01112, deoD, deoB, deoC, adh, acs

Rules

Overview: In the known pathway for deoxyinosine utilization, a phosphorylase forms deoxyribose 1-phosphate, phosphopentomutase forms deoxyribose 5-phosphate, and an aldolase produces 3-phosphoglycerate (an intermediate in glycolysis) and acetaldehyde (link). MetaCyc also describes a purine deoxyribonucleosidase (EC 3.2.2.M2), yielding deoxyribose, but this enzyme has not been linked to sequence, so it is not included in GapMind. This reaction might also occur non-specifically via ribonucleosidases. The fitness data for Paraburkholderia bryophila 376MFSha3.1 does suggest cytoplasmic hydrolysis of purine deoxynucleosides, but did not identify the deoxyribonucleosidase.

18 steps (15 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
H281DRAFT_01115 deoxynucleoside transporter, permease component 1 RLEG_RS26315 RLEG_RS03525
H281DRAFT_01114 deoxynucleoside transporter, substrate-binding component RLEG_RS26300 RLEG_RS27470
H281DRAFT_01113 deoxynucleoside transporter, ATPase component RLEG_RS26305 RLEG_RS32730
H281DRAFT_01112 deoxynucleoside transporter, permease component 2 RLEG_RS26310 RLEG_RS26350
deoD deoxyinosine phosphorylase RLEG_RS22150
deoB phosphopentomutase RLEG_RS22180
deoC deoxyribose-5-phosphate aldolase RLEG_RS11270 RLEG_RS22155
adh acetaldehyde dehydrogenase (not acylating) RLEG_RS11275 RLEG_RS18780
acs acetyl-CoA synthetase, AMP-forming RLEG_RS21015 RLEG_RS21030
Alternative steps:
ackA acetate kinase RLEG_RS17140
ald-dh-CoA acetaldehyde dehydrogenase, acylating
bmpA deoxyinosine ABC transporter, substrate-binding component RLEG_RS22125
nupA deoxyinosine ABC transporter, ATPase component RLEG_RS22130 RLEG_RS33530
nupB deoxyinosine ABC transporter, permease component 1 RLEG_RS22135 RLEG_RS33525
nupC deoxyinosine:H+ symporter NupC
nupC' deoxyinosine ABC transporter, permease component 2 RLEG_RS22140 RLEG_RS33520
nupG deoxyinosine permease NupG/XapB
pta phosphate acetyltransferase RLEG_RS00240 RLEG_RS10915

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 Apr 09 2024. 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