GapMind for catabolism of small carbon sources

 

catabolism of small carbon sources in Thiohalospira halophila HL 3

Pathways are sorted by completeness. Sort by name instead.

Pathway Steps
glutamate gltP, gdhA
alanine alsT
aspartate dauA
fumarate dauA
succinate dauA
pyruvate yjcH, actP
threonine tdcC, ltaE, adh, acs, gcvP, gcvT, gcvH, lpd
D-lactate lctP, glcD, glcE, glcF
sucrose sut, ams, scrK, glk
citrate SLC13A5, acn, icd
acetate actP, acs
asparagine ans, dauA
fructose Slc2a5, scrK
glucose MFS-glucose, glk
L-lactate lctP, L-LDH
mannose manP, manA
ethanol etoh-dh-nad, adh, acs
sorbitol SOT, sdh, scrK
cellobiose cdt, cbp, pgmA, glk
trehalose TRET1, PsTP, pgmA, glk
glucose-6-P uhpT
L-malate sdlC
2-oxoglutarate kgtP
serine serP, sdaB
gluconate gntT, gntK, gnd
maltose malEIICBA, malA, glk
mannitol PLT5, mt2d, scrK
arginine rocE, adiA, aguA, aguB, patA, patD, gabT, gabD
galactose galP, galK, galT, galE, pgmA
D-alanine cycA, dadA
glucosamine gamP, nagB
ribose rbsU, rbsK
D-serine cycA, dsdA
tryptophan aroP, tnaA
xylitol fruI, x5p-reductase
proline ectP, put1, putA
lactose lacP, lacZ, galK, galT, galE, pgmA, glk
glycerol glpF, glpK, glpD, tpi
deoxyribose deoP, deoK, deoC, adh, acs
deoxyinosine nupC, deoD, deoB, deoC, adh, acs
thymidine nupG, deoA, deoB, deoC, adh, acs
propionate putP, prpE, prpC, prpD, acn, prpB
NAG nagEcba, nagA, nagB
xylose xylT, xylA, xylB
putrescine puuP, patA, patD, gabT, gabD
arabinose araE, araA, araB, araD
histidine permease, hutH, hutU, hutI, hutG
fucose fucP, fucU, fucI, fucK, fucA, tpi, aldA
glucuronate exuT, udh, gci, kdgD, dopDH
deoxyribonate deoxyribonate-transport, deoxyribonate-dehyd, ketodeoxyribonate-cleavage, garK, aacS, atoB
lysine lysP, lat, amaB, lysN, hglS, ydiJ
rhamnose rhaT, rhaM, rhaA, rhaB, rhaD, tpi, aldA
4-hydroxybenzoate pcaK, pobA, praA, xylF, mhpD, mhpE, adh, acs
galacturonate exuT, uxaC, uxaB, uxaA, kdgK, eda
citrulline AO353_03055, AO353_03050, AO353_03045, AO353_03040, arcB, arcC, rocD, rocA
tyrosine aroP, HPD, hmgA, maiA, fahA, aacS, atoB
myoinositol iolT, iolG, iolE, iolD, iolB, iolC, iolJ, mmsA, tpi
phenylalanine aroP, PAH, PCBD, QDPR, HPD, hmgA, maiA, fahA, aacS, atoB
isoleucine Bap2, ofo, acdH, ech, ivdG, fadA, prpC, prpD, acn, prpB
leucine leuT, ilvE, ofo, liuA, liuB, liuD, liuC, liuE, aacS, atoB
valine Bap2, ofo, acdH, ech, bch, mmsB, mmsA, prpC, prpD, acn, prpB
phenylacetate paaT, paaK, paaA, paaB, paaC, paaE, paaG, paaZ1, paaZ2, paaJ1, paaF, paaH, paaJ2

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