GapMind for catabolism of small carbon sources

 

catabolism of small carbon sources in Desulfotalea psychrophila LSv54

Pathways are sorted by name. Sort by completeness instead.

Pathway Steps
acetate satP, ackA, pta
D-alanine Pf6N2E2_5402, Pf6N2E2_5403, Pf6N2E2_5404, Pf6N2E2_5405, dadA
alanine alsT
arabinose araE, araA, araB, araD
arginine rocE, rocF, rocD, PRO3, put1, putA
asparagine ans, glt
aspartate glt
cellobiose bgl, MFS-glucose, glk
citrate SLC13A5, acn, icd
citrulline AO353_03055, AO353_03050, AO353_03045, AO353_03040, arcB, arcC, rocD, PRO3, put1, putA
deoxyinosine nupC, deoD, deoB, deoC, adh, ackA, pta
deoxyribonate deoxyribonate-transport, deoxyribonate-dehyd, ketodeoxyribonate-cleavage, garK, aacS, atoB
deoxyribose deoP, deoK, deoC, adh, ackA, pta
ethanol etoh-dh-nad, adh, ackA, pta
fructose fruII-ABC, 1pfk, fba, tpi
fucose fucP, fucU, fucI, fucK, fucA, tpi, fucO
fumarate sdcL
galactose galP, galK, galT, galE, pgmA
galacturonate exuT, uxaC, uxaB, uxaA, kdgK, eda
gluconate gntT, gntK, gnd
glucose MFS-glucose, glk
glucose-6-P uhpT
glucosamine gamP, nagB
glucuronate exuT, udh, gci, kdgD, dopDH
glutamate gltP, aspA
glycerol glpF, glpK, glpD, tpi
histidine aapJ, aapQ, aapM, aapP, hutH, hutU, hutI, hutG
isoleucine brnQ, ofo, acdH, ech, ivdG, fadA, pco, hpcD, dddA, iolA
4-hydroxybenzoate pcaK, pobA, praA, xylF, mhpD, mhpE, adh, ackA, pta
D-lactate lctP, D-LDH
L-lactate lctP, DVU3033, DVU3032
lactose lacP, lacZ, galK, galT, galE, pgmA, glk
leucine aapJ, aapQ, aapM, aapP, ilvE, ofo, liuA, liuB, liuD, liuC, liuE, aacS, atoB
lysine lysP, lat, amaB, lysN, hglS, ydiJ
L-malate sdlC
maltose malEIICBA, malA, glk
mannitol mtlA, mtlD
mannose manP, manA
myoinositol iolT, iolG, iolE, iolD, iolB, iolC, iolJ, mmsA, tpi
NAG nagEcba, nagA, nagB
2-oxoglutarate kgtP
phenylacetate paaT, paaK, paaA, paaB, paaC, paaE, paaG, paaZ1, paaZ2, paaJ1, paaF, paaH, paaJ2
phenylalanine livF, livG, livH, livM, livJ, PAH, PCBD, QDPR, HPD, hmgA, maiA, fahA, aacS, atoB
proline proV, proW, proX, put1, putA
propionate lctP, prpE*, pco, hpcD, dddA, iolA
putrescine puuP, patA, patD, gabT, gabD
pyruvate SLC5A8
rhamnose rhaT, rhaM, rhaA, rhaB, rhaD, tpi, fucO
ribose rbsU, rbsK
D-serine cycA, dsdA
serine sstT, sdaB
sorbitol mtlA, srlD
succinate sdc
sucrose ams, MFS-glucose, glk
threonine sstT, ltaE, adh, ackA, pta, gcvP, gcvT, gcvH, lpd
thymidine nupG, deoA, deoB, deoC, adh, ackA, pta
trehalose treF, MFS-glucose, glk
tryptophan aroP, tnaA
tyrosine tyrP, HPD, hmgA, maiA, fahA, aacS, atoB
valine brnQ, ofo, acdH, ech, bch, mmsB, mmsA, pco, hpcD, dddA, iolA
xylitol fruI, x5p-reductase
xylose xylT, 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 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