GapMind for catabolism of small carbon sources

 

Protein WP_010936527.1 in Dehalococcoides mccartyi 195

Annotation: NCBI__GCF_000011905.1:WP_010936527.1

Length: 305 amino acids

Source: GCF_000011905.1 in NCBI

Candidate for 24 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-asparagine catabolism aatP lo Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) 35% 91% 125.9 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-aspartate catabolism aatP lo Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) 35% 91% 125.9 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-glutamate catabolism gltL lo Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) 35% 91% 125.9 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-asparagine catabolism glnQ lo 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) 31% 91% 123.6 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-isoleucine catabolism livF lo ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized) 35% 95% 122.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-leucine catabolism livF lo ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized) 35% 95% 122.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-valine catabolism livF lo ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized) 35% 95% 122.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-arginine catabolism artP lo Arginine transport ATP-binding protein ArtM (characterized) 31% 98% 121.3 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-alanine catabolism braG lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 34% 91% 119.8 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-serine catabolism braG lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 34% 91% 119.8 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-threonine catabolism braG lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 34% 91% 119.8 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-phenylalanine catabolism livF lo High-affinity branched-chain amino acid transport ATP-binding protein (characterized, see rationale) 31% 96% 115.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
D-glucosamine (chitosamine) catabolism AO353_21725 lo ABC transporter for D-glucosamine, ATPase component (characterized) 31% 92% 114 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-arabinose catabolism xylGsa lo Xylose/arabinose import ATP-binding protein XylG; EC 7.5.2.13 (characterized, see rationale) 31% 98% 112.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
D-cellobiose catabolism mglA lo glucose transporter, ATPase component (characterized) 31% 84% 110.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
D-glucose catabolism mglA lo glucose transporter, ATPase component (characterized) 31% 84% 110.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
lactose catabolism mglA lo glucose transporter, ATPase component (characterized) 31% 84% 110.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
D-maltose catabolism mglA lo glucose transporter, ATPase component (characterized) 31% 84% 110.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
sucrose catabolism mglA lo glucose transporter, ATPase component (characterized) 31% 84% 110.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
trehalose catabolism mglA lo glucose transporter, ATPase component (characterized) 31% 84% 110.5 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-arginine catabolism braG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 33% 91% 108.6 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-glutamate catabolism braG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 33% 91% 108.6 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-histidine catabolism braG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 33% 91% 108.6 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4
L-proline catabolism HSERO_RS00900 lo ABC-type branched-chain amino acid transport system, ATPase component protein (characterized, see rationale) 31% 95% 104.4 Linearmycin resistance ATP-binding protein LnrL; EC 7.6.2.- 37% 198.4

Sequence Analysis Tools

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Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

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Sequence

MVIQVQDLVKVYGPIRAVDGISFEVKKGEVFGMLGPNGAGKTTTTEIIEGLRDADSGSVT
VMGMDVRKQREQIKQLIGIQLQAPALLPLLNVEEILKLFTSFYRNSLPVDKLLEMVALTE
SRKVLSKNLSGGQQQRLSVAMAMVNNPEITFLDEPTTGLDPQARRGLWSVIEELRAQGKT
VFLTTHYMDEAERLCDRIAVVDHGKIIALDTPKKLISSNFKESAIEFEMEPVPSGELLGS
FPCVTSASVEGFEVILYSADVPKTMGAILDYADKNKGNTELRNLHVRQATLEDVFLKLTG
RKIRE

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