GapMind for catabolism of small carbon sources

 

catabolism of small carbon sources in Thermophagus xiamenensis HS1

Pathways are sorted by completeness. Sort by name instead.

Pathway Steps
galactose sglS, galK, galT, galE, pgmA
arabinose Echvi_1880, araA, araB, araD
maltose malI, malP, pgmB, glk
trehalose BT2158, klh, SSS-glucose, glk
cellobiose bgl, SSS-glucose, glk
xylose xylT, xylA, xylB
glucose SSS-glucose, glk
alanine alsT
asparagine ans, glt
fructose BT1758, scrK
aspartate glt
lactose lacP, lacZ, galK, galT, galE, pgmA, glk
threonine tdcC, tdh, kbl, gcvP, gcvT, gcvH, lpd
rhamnose rhaT, rhaM, rhaA, rhaB, rhaD, tpi, aldA
glucuronate dctP, dctQ, dctM, uxaC, uxuB, uxuA, kdgK, eda
arginine rocE, arcA, arcB, arcC, rocD, rocA
acetate actP, ackA, pta
citrate SLC13A5, acn, icd
sucrose ams, SSS-glucose, glk
deoxyinosine nupC, deoD, deoB, deoC, adh, ackA, pta
propionate putP, prpE, pccA, pccB, epi, mcm-large, mcm-small
ethanol etoh-dh-nad, adh, ackA, pta
NAG nagP, nagK, nagA, nagB
glucosamine nagX, nagP, nagK, nagA, nagB
glutamate gltS, gdhA
D-lactate lctP, D-LDH
mannitol mtlA, mtlD
mannose STP6, mannokinase, manA
proline proY, put1, putA
fumarate dctA
glucose-6-P uhpT
L-malate sdlC
2-oxoglutarate kgtP
pyruvate SLC5A8
succinate sdc
L-lactate lctP, L-LDH
D-serine cycA, dsdA
serine serP, sdaB
sorbitol mtlA, srlD
isoleucine Bap2, vorA*, vorB, vorC, acdH, ech, ivdG, fadA, pccA, pccB, epi, mcm-large, mcm-small
leucine leuT, ilvE, vorA*, vorB, vorC, liuA, liuB, liuD, liuC, liuE, aacS, atoB
deoxyribose deoP, deoK, deoC, adh, ackA, pta
galacturonate exuT, uxaC, uxaB, uxaA, kdgK, eda
gluconate gntT, gntK, gnd
xylitol PLT5, xdhA, xylB
fucose fucP, fucU, fucI, fucK, fucA, tpi, aldA
thymidine nupC, deoA, deoB, deoC, adh, ackA, pta
glycerol glpF, dhaD, dhaK', tpi
D-alanine cycA, dadA
ribose rbsU, rbsK
tryptophan aroP, tnaA
valine Bap2, vorA*, vorB, vorC, acdH, ech, bch, mmsB, mmsA, pccA, pccB, epi, mcm-large, mcm-small
citrulline AO353_03055, AO353_03050, AO353_03045, AO353_03040, arcB, arcC, rocD, rocA
deoxyribonate deoxyribonate-transport, deoxyribonate-dehyd, ketodeoxyribonate-cleavage, garK, aacS, atoB
histidine permease, hutH, hutU, hutI, hutG
putrescine puuP, patA, patD, gabT, gabD
lysine lysP, lat, amaB, lysN, hglS, ydiJ
myoinositol iolT, iolG, iolM, iolN, iolO, uxaE, uxuB, uxuA, kdgK, eda
tyrosine aroP, HPD, hmgA, maiA, fahA, aacS, atoB
4-hydroxybenzoate pcaK, pobA, praA, xylF, mhpD, mhpE, adh, ackA, pta
phenylalanine aroP, PAH, PCBD, QDPR, HPD, hmgA, maiA, fahA, aacS, atoB
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