Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
L-histidine catabolism | PA5503 | med | Methionine import ATP-binding protein MetN 2, component of L-Histidine uptake porter, MetIQN (characterized) | 44% | 96% | 263.1 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-arginine catabolism | artP | med | Arginine transport ATP-binding protein ArtM (characterized) | 40% | 99% | 184.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-asparagine catabolism | glnQ | med | Glutamine ABC transporter ATP-binding protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized) | 42% | 96% | 184.1 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-glutamate catabolism | gltL | med | Glutamine ABC transporter ATP-binding protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized) | 42% | 96% | 184.1 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-mannose catabolism | TM1750 | lo | TM1750, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized) | 39% | 75% | 173.7 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-histidine catabolism | BPHYT_RS24015 | lo | ABC transporter related (characterized, see rationale) | 38% | 94% | 171.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-cellobiose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-galactose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-glucose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
lactose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-maltose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-mannose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
sucrose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
trehalose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 38% | 72% | 170.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-histidine catabolism | hisP | lo | Histidine transport ATP-binding protein HisP (characterized) | 37% | 95% | 170.2 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-lysine catabolism | hisP | lo | Histidine transport ATP-binding protein HisP (characterized) | 37% | 95% | 170.2 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-asparagine catabolism | peb1C | lo | PEB1C, component of Uptake system for glutamate and aspartate (characterized) | 37% | 98% | 166 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-aspartate catabolism | peb1C | lo | PEB1C, component of Uptake system for glutamate and aspartate (characterized) | 37% | 98% | 166 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-proline catabolism | proV | lo | Glycine betaine/proline betaine transport system ATP-binding protein ProV (characterized) | 37% | 67% | 165.2 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
putrescine catabolism | potA | lo | PotG aka B0855, component of Putrescine porter (characterized) | 39% | 62% | 165.2 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-arabinose catabolism | araV | lo | AraV, component of Arabinose, fructose, xylose porter (characterized) | 34% | 84% | 162.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-fructose catabolism | araV | lo | AraV, component of Arabinose, fructose, xylose porter (characterized) | 34% | 84% | 162.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
sucrose catabolism | araV | lo | AraV, component of Arabinose, fructose, xylose porter (characterized) | 34% | 84% | 162.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-xylose catabolism | araV | lo | AraV, component of Arabinose, fructose, xylose porter (characterized) | 34% | 84% | 162.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-asparagine catabolism | aapP | lo | AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) | 36% | 92% | 162.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-aspartate catabolism | aapP | lo | AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) | 36% | 92% | 162.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-citrulline catabolism | AO353_03040 | lo | ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized) | 34% | 98% | 162.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-glutamate catabolism | aapP | lo | AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) | 36% | 92% | 162.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-histidine catabolism | aapP | lo | AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) | 36% | 92% | 162.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-leucine catabolism | aapP | lo | AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) | 36% | 92% | 162.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-proline catabolism | aapP | lo | AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) | 36% | 92% | 162.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-asparagine catabolism | aatP | lo | Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) | 37% | 98% | 159.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-aspartate catabolism | aatP | lo | Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) | 37% | 98% | 159.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-alanine catabolism | Pf6N2E2_5405 | lo | ABC transporter for D-Alanine, ATPase component (characterized) | 35% | 94% | 158.7 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-asparagine catabolism | bgtA | lo | ATPase (characterized, see rationale) | 38% | 91% | 157.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-aspartate catabolism | bgtA | lo | ATPase (characterized, see rationale) | 38% | 91% | 157.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-citrulline catabolism | PS417_17605 | lo | ATP-binding cassette domain-containing protein; SubName: Full=Amino acid transporter; SubName: Full=Histidine ABC transporter ATP-binding protein; SubName: Full=Histidine transport system ATP-binding protein (characterized, see rationale) | 36% | 88% | 156.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-glucosamine (chitosamine) catabolism | AO353_21725 | lo | ABC transporter for D-glucosamine, ATPase component (characterized) | 35% | 94% | 156 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-histidine catabolism | hutV | lo | ABC transporter for L-Histidine, ATPase component (characterized) | 36% | 95% | 156 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-proline catabolism | opuBA | lo | BusAA, component of Uptake system for glycine-betaine (high affinity) and proline (low affinity) (OpuAA-OpuABC) or BusAA-ABC of Lactococcus lactis). BusAA, the ATPase subunit, has a C-terminal tandem cystathionine β-synthase (CBS) domain which is the cytoplasmic K+ sensor for osmotic stress (osmotic strength)while the BusABC subunit has the membrane and receptor domains fused to each other (Biemans-Oldehinkel et al., 2006; Mahmood et al., 2006; Gul et al. 2012). An N-terminal amphipathic α-helix of OpuA is necessary for high activity but is not critical for biogenesis or the ionic regulation of transport (characterized) | 35% | 54% | 154.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-histidine catabolism | bgtA | lo | BgtA aka SLR1735, component of Arginine/lysine/histidine/glutamine porter (characterized) | 37% | 94% | 149.1 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-mannose catabolism | TM1749 | lo | TM1749, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized) | 33% | 81% | 145.6 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-cellobiose catabolism | cbtD | lo | CbtD, component of Cellobiose and cellooligosaccharide porter (characterized) | 35% | 73% | 143.3 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-maltose catabolism | thuK | lo | Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized) | 30% | 81% | 141.7 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
trehalose catabolism | thuK | lo | Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized) | 30% | 81% | 141.7 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-proline catabolism | hutV | lo | HutV aka HISV aka R02702 aka SMC00670, component of Uptake system for hisitidine, proline, proline-betaine and glycine-betaine (characterized) | 33% | 95% | 139.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-cellobiose catabolism | cbtF | lo | CbtF, component of Cellobiose and cellooligosaccharide porter (characterized) | 31% | 86% | 137.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-tryptophan catabolism | ecfA1 | lo | Energy-coupling factor transporter ATP-binding protein EcfA1; Short=ECF transporter A component EcfA; EC 7.-.-.- (characterized, see rationale) | 37% | 78% | 137.1 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-maltose catabolism | malK1 | lo | MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized) | 32% | 65% | 136.3 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-alanine catabolism | braF | lo | NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 35% | 90% | 134.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-histidine catabolism | natA | lo | NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 35% | 90% | 134.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-leucine catabolism | natA | lo | NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 35% | 90% | 134.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-proline catabolism | natA | lo | NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 35% | 90% | 134.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-serine catabolism | braF | lo | NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 35% | 90% | 134.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-sorbitol (glucitol) catabolism | mtlK | lo | ABC transporter for D-Sorbitol, ATPase component (characterized) | 31% | 80% | 134.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-threonine catabolism | braF | lo | NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 35% | 90% | 134.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-mannitol catabolism | mtlK | lo | SmoK aka POLK, component of Hexitol (glucitol; mannitol) porter (characterized) | 32% | 72% | 134 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-isoleucine catabolism | livG | lo | ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized) | 31% | 99% | 131.7 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-leucine catabolism | livG | lo | ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized) | 31% | 99% | 131.7 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-valine catabolism | livG | lo | ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized) | 31% | 99% | 131.7 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-tryptophan catabolism | ecfA2 | lo | Energy-coupling factor transporter ATP-binding protein EcfA2; Short=ECF transporter A component EcfA2; EC 7.-.-.- (characterized, see rationale) | 35% | 79% | 127.5 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-isoleucine catabolism | natA | lo | NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 32% | 88% | 125.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-valine catabolism | natA | lo | NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 32% | 88% | 125.9 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
2'-deoxyinosine catabolism | nupA | lo | RnsB, component of The (deoxy)ribonucleoside permease; probably takes up all deoxy- and ribonucleosides (cytidine, uridine, adenosine and toxic analogues, fluorocytidine and fluorouridine tested), but not ribose or nucleobases (characterized) | 31% | 53% | 124.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-proline catabolism | HSERO_RS00895 | lo | ABC-type branched-chain amino acid transport system, ATPase component protein (characterized, see rationale) | 31% | 98% | 124.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-arabinose catabolism | xylGsa | lo | Xylose/arabinose import ATP-binding protein XylG; EC 7.5.2.13 (characterized, see rationale) | 33% | 86% | 121.3 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-phenylalanine catabolism | livG | lo | ABC transporter ATP-binding protein (characterized, see rationale) | 30% | 96% | 114.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-serine catabolism | Ac3H11_1693 | lo | ABC transporter ATP-binding protein (characterized, see rationale) | 30% | 96% | 114.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
L-tyrosine catabolism | Ac3H11_1693 | lo | ABC transporter ATP-binding protein (characterized, see rationale) | 30% | 96% | 114.8 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-cellobiose catabolism | mglA | lo | glucose transporter, ATPase component (characterized) | 31% | 88% | 114.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-glucose catabolism | mglA | lo | glucose transporter, ATPase component (characterized) | 31% | 88% | 114.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
lactose catabolism | mglA | lo | glucose transporter, ATPase component (characterized) | 31% | 88% | 114.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
D-maltose catabolism | mglA | lo | glucose transporter, ATPase component (characterized) | 31% | 88% | 114.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
sucrose catabolism | mglA | lo | glucose transporter, ATPase component (characterized) | 31% | 88% | 114.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
trehalose catabolism | mglA | lo | glucose transporter, ATPase component (characterized) | 31% | 88% | 114.4 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
glycerol catabolism | glpS | lo | ABC transporter for Glycerol, ATPase component 1 (characterized) | 32% | 56% | 105.1 | Methionine import ATP-binding protein MetN; EC 7.4.2.11 | 51% | 351.3 |
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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.
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).
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know