GapMind for catabolism of small carbon sources

 

catabolism of small carbon sources in Intestinibacter bartlettii DSM 16795

Pathways are sorted by name. Sort by completeness instead.

Pathway Steps
acetate actP, ackA, pta
D-alanine cycA, dadA
alanine alsT
arabinose araE, araA, araB, araD
arginine rocE, rocF, rocD, PRO3, put1*, putA
asparagine ans, glt
aspartate glt
cellobiose bgl, ptsG-crr
citrate SLC13A5, acn, icd
citrulline AO353_03055, AO353_03050, AO353_03045, AO353_03040, arcB, arcC, rocD, PRO3, put1*, putA
deoxyinosine nupA, nupB, nupC', bmpA, deoD, deoB, deoC, ald-dh-CoA
deoxyribonate deoxyribonate-transport, deoxyribonate-dehyd, ketodeoxyribonate-cleavage, garK, aacS, atoB
deoxyribose deoP, deoK, deoC, ald-dh-CoA
ethanol etoh-dh-nad, ald-dh-CoA
fructose fruII-ABC, 1pfk, fba, tpi
fucose fucP, fucU, fucI, fucK, fucA, tpi, fucO
fumarate dctA
galactose galP, galK, galT, galE, pgmA
galacturonate exuT, uxaC, uxaB, uxaA, kdgK, eda
gluconate gntT, gntK, edd, eda
glucose ptsG-crr
glucose-6-P uhpT
glucosamine gamP, nagB
glucuronate exuT, uxaC, uxuB, uxuA, kdgK, eda
glutamate gltP, gdhA
glycerol glpF, glpK, glpO, tpi
histidine LAT2, hutH, hutU, hutI, hutG
isoleucine brnQ, vorA*, vorB, vorC, acdH, ech, ivdG, fadA, pccA, pccB, epi, mcmA
4-hydroxybenzoate pcaK, pobA, praA, xylF, mhpD, mhpE, ald-dh-CoA
D-lactate lctP, lctB, lctC, lctD
L-lactate lctP, L-LDH
lactose lacP, lacZ, galK, galT, galE, pgmA, glk
leucine leuT, ilvE, vorA*, vorB, vorC, liuA, liuB, liuD, liuC, liuE, aacS, atoB
lysine lysP, lat, amaB, lysN, hglS, ydiJ
L-malate sdlC
maltose susB, ptsG-crr
mannitol cmtA, cmtB, mtlD
mannose manP, manA
myoinositol iolT, iolG, iolM, iolN, iolO, uxaE, uxuB, uxuA, kdgK, eda
NAG nagEcba, nagA, nagB
2-oxoglutarate kgtP
phenylacetate paaT, paaK, paaA, paaB, paaC, paaE, paaG, paaZ1, paaZ2, paaJ1, paaF, paaH, paaJ2
phenylalanine aroP, PAH, PCBD, QDPR, HPD, hmgA, maiA, fahA, aacS, atoB
proline putP, put1*, putA
propionate putP, prpE, pccA, pccB, epi, mcmA
putrescine potA, potB, potC, potD, patA, patD, gabT, gabD
pyruvate SLC5A8
rhamnose rhaT, rhaM, rhaA, rhaB, rhaD, tpi, fucO
ribose rbsA, rbsB, rbsC, rbsK
D-serine cycA, dsdA
serine serP, sdaB
sorbitol srlA, srlB, srlE, srlD
succinate sdc
sucrose ams, fruII-ABC, 1pfk, fba, tpi
threonine tdcC, ltaE, ald-dh-CoA, gcvP, gcvT, gcvH, lpd
thymidine nupC, deoA, deoB, deoC, ald-dh-CoA
trehalose treF, ptsG-crr
tryptophan trpP, ecfA1, ecfA2, ecfT, tnaA
tyrosine tyt1, HPD, hmgA, maiA, fahA, aacS, atoB
valine brnQ, vorA*, vorB, vorC, acdH, ech, bch, mmsB, mmsA, pccA, pccB, epi, mcmA
xylitol fruI, x5p-reductase
xylose xylF, xylG, xylH, xylA, xylB

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 Jun 28 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