Potential Gaps in catabolism of small carbon sources in Pseudoalteromonas arctica A 37-1-2
Found 87 low-confidence and 31 medium-confidence steps on the best paths for 62 pathways.
Pathway | Step | Best candidate | 2nd candidate |
2-oxoglutarate | kgtP: 2-oxoglutarate:H+ symporter KgtP | | |
4-hydroxybenzoate | mhpD: 2-hydroxypentadienoate hydratase | | |
4-hydroxybenzoate | mhpE: 4-hydroxy-2-oxovalerate aldolase | PARC_RS00705 | |
4-hydroxybenzoate | pcaK: 4-hydroxybenzoate transporter pcaK | | |
4-hydroxybenzoate | pobA: 4-hydroxybenzoate 3-monooxygenase | | |
4-hydroxybenzoate | praA: protocatechuate 2,3-dioxygenase | | |
4-hydroxybenzoate | xylF: 2-hydroxymuconate semialdehyde hydrolase | PARC_RS08880 | |
acetate | actP: cation/acetate symporter ActP | PARC_RS14125 | |
arabinose | aldA: (glycol)aldehyde dehydrogenase | PARC_RS09315 | PARC_RS20260 |
arabinose | Echvi_1880: L-arabinose:Na+ symporter | PARC_RS07465 | |
arabinose | gyaR: glyoxylate reductase | PARC_RS13645 | PARC_RS15170 |
arabinose | KDG-aldolase: 2-dehydro-3-deoxy-L-arabinonate aldolase | | |
arabinose | xacB: L-arabinose 1-dehydrogenase | PARC_RS01100 | PARC_RS10530 |
arabinose | xacC: L-arabinono-1,4-lactonase | PARC_RS19220 | |
arabinose | xacD: L-arabinonate dehydratase | PARC_RS09910 | PARC_RS15950 |
arginine | astC: succinylornithine transaminase | PARC_RS01180 | PARC_RS20300 |
arginine | rocE: L-arginine permease | | |
citrate | cit1: citrate:H+ symporter Cit1 | PARC_RS18590 | |
citrulline | AO353_03040: ABC transporter for L-Citrulline, ATPase component | PARC_RS03635 | PARC_RS15615 |
citrulline | AO353_03045: ABC transporter for L-Citrulline, permease component 2 | | |
citrulline | AO353_03050: ABC transporter for L-Citrulline, permease component 1 | | |
citrulline | AO353_03055: ABC transporter for L-Citrulline, periplasmic substrate-binding component | | |
citrulline | citrullinase: putative citrullinase | PARC_RS10665 | |
citrulline | rocD: ornithine aminotransferase | PARC_RS20300 | PARC_RS01180 |
D-alanine | cycA: D-alanine:H+ symporter CycA | | |
D-alanine | dadA: D-alanine dehydrogenase | | |
D-lactate | lctP: D-lactate:H+ symporter LctP or LidP | | |
D-serine | cycA: D-serine:H+ symporter CycA | | |
D-serine | dsdA: D-serine ammonia-lyase | PARC_RS01655 | |
deoxyribonate | deoxyribonate-dehyd: 2-deoxy-D-ribonate 3-dehydrogenase | PARC_RS01100 | PARC_RS10020 |
deoxyribonate | deoxyribonate-transport: 2-deoxy-D-ribonate transporter | | |
deoxyribonate | ketodeoxyribonate-cleavage: 2-deoxy-3-keto-D-ribonate cleavage enzyme | | |
deoxyribose | deoK: deoxyribokinase | | |
deoxyribose | deoP: deoxyribose transporter | PARC_RS20795 | PARC_RS07190 |
fucose | aldA: lactaldehyde dehydrogenase | PARC_RS09315 | PARC_RS18845 |
fucose | fucA: L-fuculose-phosphate aldolase FucA | PARC_RS00545 | |
fucose | fucI: L-fucose isomerase FucI | | |
fucose | fucK: L-fuculose kinase FucK | | |
fucose | fucP: L-fucose:H+ symporter FucP | PARC_RS20795 | PARC_RS07190 |
fucose | fucU: L-fucose mutarotase FucU | | |
galacturonate | exuT: D-galacturonate transporter ExuT | PARC_RS11445 | |
galacturonate | kdgK: 2-keto-3-deoxygluconate kinase | PARC_RS11440 | PARC_RS09430 |
galacturonate | uxaA: D-altronate dehydratase | | |
galacturonate | uxaB: tagaturonate reductase | PARC_RS18740 | |
galacturonate | uxaC: D-galacturonate isomerase | | |
glucosamine | gamP: glucosamine PTS system, EII-CBA components (GamP/NagE) | | |
glucosamine | nagB: glucosamine 6-phosphate deaminase (isomerizing) | PARC_RS17365 | |
glucose-6-P | uhpT: glucose-6-phosphate:phosphate antiporter | | |
glucuronate | exuT: D-glucuronate:H+ symporter ExuT | PARC_RS11445 | |
glucuronate | kdgK: 2-keto-3-deoxygluconate kinase | PARC_RS11440 | PARC_RS09430 |
glucuronate | uxaC: D-glucuronate isomerase | | |
glucuronate | uxuA: D-mannonate dehydratase | PARC_RS15950 | PARC_RS09565 |
glucuronate | uxuB: D-mannonate dehydrogenase | PARC_RS18740 | |
glycerol | glpF: glycerol facilitator glpF | | |
histidine | hutG: N-formiminoglutamate formiminohydrolase | PARC_RS01815 | |
histidine | permease: L-histidine permease | | |
isoleucine | Bap2: L-isoleucine permease Bap2 | | |
L-lactate | lctO: L-lactate oxidase or 2-monooxygenase | | |
lactose | lacY: lactose:proton symporter LacY | PARC_RS02350 | |
leucine | leuT: L-leucine:Na+ symporter LeuT | PARC_RS07245 | |
lysine | amaB: L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) | PARC_RS02425 | PARC_RS09315 |
lysine | hglS: D-2-hydroxyglutarate synthase | | |
lysine | lat: L-lysine 6-aminotransferase | PARC_RS20300 | PARC_RS01180 |
lysine | lysN: 2-aminoadipate transaminase | PARC_RS01180 | PARC_RS20300 |
lysine | lysP: L-lysine:H+ symporter LysP | | |
mannitol | mtlG: polyol ABC transporter, permease component 2 (MtlG/SmoG) | PARC_RS08895 | |
mannose | gluP: mannose:Na+ symporter | PARC_RS20795 | PARC_RS07190 |
myoinositol | iolB: 5-deoxy-D-glucuronate isomerase | | |
myoinositol | iolC: 5-dehydro-2-deoxy-D-gluconate kinase | | |
myoinositol | iolD: 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase | | |
myoinositol | iolE: scyllo-inosose 2-dehydratase | | |
myoinositol | iolG: myo-inositol 2-dehydrogenase | | |
myoinositol | iolJ: 5-dehydro-2-deoxyphosphogluconate aldolase | PARC_RS14085 | |
myoinositol | iolT: myo-inositol:H+ symporter | PARC_RS05575 | PARC_RS02340 |
NAG | nagA: N-acetylglucosamine 6-phosphate deacetylase | | |
NAG | nagB: glucosamine 6-phosphate deaminase (isomerizing) | PARC_RS17365 | |
NAG | nagEcba: N-acetylglucosamine phosphotransferase system, EII-CBA components | | |
phenylacetate | paaA: phenylacetyl-CoA 1,2-epoxidase, subunit A | | |
phenylacetate | paaB: phenylacetyl-CoA 1,2-epoxidase, subunit B | | |
phenylacetate | paaC: phenylacetyl-CoA 1,2-epoxidase, subunit C | | |
phenylacetate | paaE: phenylacetyl-CoA 1,2-epoxidase, subunit E | | |
phenylacetate | paaF: 2,3-dehydroadipyl-CoA hydratase | PARC_RS09095 | PARC_RS12325 |
phenylacetate | paaG: 1,2-epoxyphenylacetyl-CoA isomerase / 2-(oxepinyl)acetyl-CoA isomerase / didehydroadipyl-CoA isomerase | PARC_RS04290 | PARC_RS09130 |
phenylacetate | paaJ1: 3-oxo-5,6-dehydrosuberyl-CoA thiolase | PARC_RS00050 | PARC_RS08685 |
phenylacetate | paaJ2: 3-oxoadipyl-CoA thiolase | PARC_RS00050 | PARC_RS08685 |
phenylacetate | paaK: phenylacetate-CoA ligase | PARC_RS20720 | |
phenylacetate | paaT: phenylacetate transporter Paa | | |
phenylacetate | paaZ1: oxepin-CoA hydrolase | PARC_RS09095 | |
phenylacetate | paaZ2: 3-oxo-5,6-didehydrosuberyl-CoA semialdehyde dehydrogenase | | |
phenylalanine | aroP: L-phenylalanine:H+ symporter AroP | | |
propionate | putP: propionate transporter; proline:Na+ symporter | PARC_RS04895 | |
putrescine | gabT: gamma-aminobutyrate transaminase | PARC_RS01180 | PARC_RS20300 |
putrescine | patA: putrescine aminotransferase (PatA/SpuC) | PARC_RS01180 | PARC_RS20300 |
putrescine | patD: gamma-aminobutyraldehyde dehydrogenase | PARC_RS20260 | PARC_RS18845 |
putrescine | puuP: putrescine:H+ symporter PuuP/PlaP | | |
pyruvate | actP: large subunit of pyruvate transporter (actP-like) | PARC_RS14125 | |
pyruvate | yjcH: putative small subunit of pyruvate transporter (yjcH-like) | PARC_RS14130 | |
rhamnose | aldA: lactaldehyde dehydrogenase | PARC_RS09315 | PARC_RS18845 |
rhamnose | rhaA: L-rhamnose isomerase | | |
rhamnose | rhaB: L-rhamnulokinase | | |
rhamnose | rhaD: rhamnulose 1-phosphate aldolase | | |
rhamnose | rhaM: L-rhamnose mutarotase | | |
ribose | rbsK: ribokinase | | |
ribose | rbsU: probable D-ribose transporter RbsU | | |
sorbitol | sdh: sorbitol dehydrogenase | PARC_RS18740 | PARC_RS13765 |
threonine | snatA: L-threonine transporter snatA | PARC_RS02930 | PARC_RS08735 |
trehalose | treF: trehalase | PARC_RS09975 | |
tryptophan | aroP: tryptophan:H+ symporter AroP | | |
tryptophan | tnaA: tryptophanase | | |
valine | acdH: isobutyryl-CoA dehydrogenase | PARC_RS09100 | PARC_RS09120 |
valine | Bap2: L-valine permease Bap2 | | |
valine | ech: (S)-3-hydroxybutanoyl-CoA hydro-lyase | PARC_RS09095 | PARC_RS12325 |
valine | mmsB: 3-hydroxyisobutyrate dehydrogenase | PARC_RS09085 | PARC_RS06645 |
xylitol | fruI: xylitol PTS, enzyme IIABC (FruI) | | |
xylitol | x5p-reductase: D-xylulose-5-phosphate 2-reductase | PARC_RS13765 | PARC_RS09325 |
xylose | xylA: xylose isomerase | | |
xylose | xylB: xylulokinase | | |
xylose | xylT: D-xylose transporter | PARC_RS05575 | PARC_RS02340 |
Confidence: high confidence medium confidence low confidence
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:
- ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
- HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.
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:
- ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
- ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
- HMMer finds a hit (regardless of coverage or other bits).
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:
- our ignorance of proteins' functions,
- omissions in the gene models,
- frame-shift errors in the genome sequence, or
- the organism lacks the pathway.
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