GapMind for catabolism of small carbon sources

 

D-fructose catabolism in Cronobacter universalis NCTC 9529

Best path

fruA, fruB, 1pfk, fba, tpi

Rules

Overview: Many bacteria take up fructose by a phosphotransferase (PTS) system that forms fructose 1-phosphate; this can be consumed via 1-phosphofructokinase and glycolysis (link). Alternatively, some PTS systems form fructose 6-phosphate, which is a central metabolic intermediate. Fructose can also be taken up directly and then phosphorylated to fructose 6-phosphate, a central metabolic intermediate. Another path is known in Aeromonas hydrophila -- phosphofructomutase converts fructose 1-phosphate (formed by a PTS system) to fructose 6-phosphate (PMID:9579084). This path is not included in GapMind because phosphofructomutase has not been linked to sequence. Also, in eukaryotes, fructose-1,6-bisphosphate aldolase is reported to cleave fructose 1-phosphate to glycerone phosphate and glyceraldehyde (link). This would make 1-phosphofructokinase unnececessary. It's not clear that this occurs in prokaryotes, so this is not listed.

37 steps (27 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
fruA fructose-specific PTS system (fructose 1-phosphate forming), EII-B'BC components AFK65_RS13270
fruB fructose-specific PTS system (fructose 1-phosphate forming), Hpr and EII-A components AFK65_RS13280
1pfk 1-phosphofructokinase AFK65_RS13275 AFK65_RS08360
fba fructose 1,6-bisphosphate aldolase AFK65_RS16005 AFK65_RS13015
tpi triose-phosphate isomerase AFK65_RS00405 AFK65_RS16010
Alternative steps:
araS fructose ABC transporter, substrate-binding component AraS
araT fructose ABC transporter, permease component 2 (AraT)
araU fructose ABC transporter, permease component 1 (AraU)
araV fructose ABC transporter, ATPase component AraV AFK65_RS18480 AFK65_RS05695
BT1758 fructose transporter
ffz fructose facilitator (uniporter)
frcA fructose ABC transporter, ATPase component FrcA AFK65_RS19710 AFK65_RS12175
frcB fructose ABC transporter, substrate-binding component FrcB
frcC fructose ABC transporter, permease component FrcC AFK65_RS19705 AFK65_RS13205
frt1 fructose:H+ symporter Frt1 AFK65_RS04490 AFK65_RS16050
fruD fructose-specific PTS system (fructose 1-phosphate forming), EII-A component
fruE fructose ABC transporter, substrate-binding component FruE AFK65_RS16910
fruF fructose ABC transporter, permease component 1 (FruF) AFK65_RS16900 AFK65_RS19705
fruG fructose ABC transporter, permease component 2 (FruG) AFK65_RS16895 AFK65_RS19705
fruI fructose-specific PTS system (fructose 1-phosphate forming), EI, Hpr, and EII-A components AFK65_RS14170 AFK65_RS15665
fruII-A fructose-specific PTS system (fructose 1-phosphate forming), EII-A component AFK65_RS02010
fruII-ABC fructose-specific PTS system (fructose 1-phosphate forming), EII-ABC components AFK65_RS13270
fruII-B fructose-specific PTS system (fructose 1-phosphate forming), EII-B component AFK65_RS13270
fruII-C fructose-specific PTS system (fructose 1-phosphate forming), EII-C component AFK65_RS13270
fruK fructose ABC transporter, ATPase component FruK AFK65_RS16905 AFK65_RS19710
fruP fructose porter FruP
ght6 high-affinity fructose transporter ght6
glcP fructose:H+ symporter GlcP AFK65_RS04490 AFK65_RS16050
levD fructose PTS system (fructose 6-phosphate forming), EII-A component AFK65_RS11735
levDE fructose PTS system (fructose 6-phosphate forming), EII-AB component AFK65_RS11735
levE fructose PTS system (fructose 6-phosphate forming), EII-B component AFK65_RS11735
levF fructose PTS system (fructose 6-phosphate forming), EII-C component AFK65_RS11740
levG fructose PTS system (fructose 6-phosphate forming), EII-D component AFK65_RS11745
scrK fructokinase AFK65_RS04815 AFK65_RS02370
Slc2a5 fructose:H+ symporter AFK65_RS16050 AFK65_RS04490
STP6 sugar transport protein 6 AFK65_RS16050 AFK65_RS04760
THT2A fructose THT2A

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