GapMind for catabolism of small carbon sources

 

catabolism of small carbon sources in Pedobacter arcticus A12

Pathways are sorted by completeness. Sort by name instead.

Pathway Steps
glucosamine nagX, nagP, nagK, nagA, nagB
NAG nagP, nagK, nagA, nagB
xylose Echvi_1871, xylA, xylB
asparagine ans, glt
glutamate gltS, gdhA
aspartate glt
fumarate sdcL
L-malate sdlC
succinate sdc
glycerol glpF, glpK, glpD, tpi
cellobiose bgl, MFS-glucose, glk
ethanol etoh-dh-nad, adh, acs
maltose susB, MFS-glucose, glk
proline N515DRAFT_2924, put1, putA
acetate dctA, acs
glucose MFS-glucose, glk
trehalose treF, MFS-glucose, glk
alanine alsT
glucose-6-P uhpT
mannose gluP, mannokinase, manA
rhamnose rhaT, rhaM, rhaA, rhaB, rhaD, tpi, aldA
threonine tdcC, tdh, kbl, gcvP, gcvT, gcvH, lpd
galacturonate exuT, uxaC, uxaB, uxaA, kdgK, eda
fucose fucP, fucU, fdh, fuconolactonase, fucD, fucDH, KDF-hydrolase
galactose HP1174, galK, galT, galE, pgmA
glucuronate exuT, uxaC, uxuB, uxuA, kdgK, eda
deoxyinosine nupG, deoD, deoB, deoC, adh, acs
citrate SLC13A5, acn, icd
lactose lacP, lacZ, galK, galT, galE, pgmA, glk
L-lactate lctP, lldE, lldF, lldG
D-lactate lctP, D-LDH
serine serP, sdaB
sucrose ams, MFS-glucose, glk
fructose fruII-ABC, 1pfk, fba, tpi
2-oxoglutarate kgtP
pyruvate SLC5A8
arginine rocE, rocF, rocD, PRO3, put1, putA
thymidine nupG, deoA, deoB, deoC, adh, acs
gluconate gntT, gntK, gnd
xylitol PLT5, xdhA, xylB
arabinose Echvi_1880, araA, araB, araD
deoxyribose deoP, deoK, deoC, adh, acs
D-alanine cycA, dadA
mannitol mtlA, mtlD
ribose rbsU, rbsK
D-serine cycA, dsdA
sorbitol mtlA, srlD
tryptophan aroP, tnaA
lysine lysP, lat, amaB, lysN, hglS, ydiJ
propionate putP, prpE, pco, hpcD, dddA, iolA
putrescine puuP, patA, patD, gabT, gabD
citrulline AO353_03055, AO353_03050, AO353_03045, AO353_03040, citrullinase, rocD, PRO3, put1, putA
isoleucine Bap2, bkdA, bkdB, bkdC, lpd, acdH, ech, ivdG, fadA, pco, hpcD, dddA, iolA
valine Bap2, bkdA, bkdB, bkdC, lpd, acdH, ech, bch, mmsB, mmsA, pco, hpcD, dddA, iolA
4-hydroxybenzoate pcaK, pobA, praA, xylF, mhpD, mhpE, adh, acs
histidine permease, hutH, hutU, hutI, hutG
deoxyribonate deoxyribonate-transport, deoxyribonate-dehyd, ketodeoxyribonate-cleavage, garK, aacS, atoB
leucine leuT, ilvE, bkdA, bkdB, bkdC, lpd, liuA, liuB, liuD, liuC, liuE, aacS, atoB
myoinositol iolT, iolG, iolM, iolN, iolO, uxaE, uxuB, uxuA, kdgK, eda
tyrosine aroP, HPD, hmgA, maiA, fahA, aacS, atoB
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