GapMind for catabolism of small carbon sources

 

Protein WP_072910078.1 in Malonomonas rubra DSM 5091

Annotation: NCBI__GCF_900142125.1:WP_072910078.1

Length: 244 amino acids

Source: GCF_900142125.1 in NCBI

Candidate for 35 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
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) 60% 97% 285.4 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
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) 60% 97% 285.4 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-arginine catabolism artP med Arginine transport ATP-binding protein ArtM (characterized) 59% 100% 280.8 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-asparagine catabolism bgtA med ATPase (characterized, see rationale) 62% 88% 279.3 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-aspartate catabolism bgtA med ATPase (characterized, see rationale) 62% 88% 279.3 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-asparagine catabolism aatP med Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) 58% 99% 278.1 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-aspartate catabolism aatP med Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) 58% 99% 278.1 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-lysine catabolism hisP med Amino-acid ABC transporter, ATP-binding protein (characterized, see rationale) 57% 92% 270 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-histidine catabolism aapP med ABC transporter for L-Glutamine, L-Histidine, and other L-amino acids, ATPase component (characterized) 61% 86% 263.8 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-asparagine catabolism aapP med 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) 60% 86% 263.1 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-aspartate catabolism aapP med 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) 60% 86% 263.1 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-glutamate catabolism aapP med 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) 60% 86% 263.1 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-leucine catabolism aapP med 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) 60% 86% 263.1 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-proline catabolism aapP med 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) 60% 86% 263.1 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-asparagine catabolism bztD med BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 60% 84% 261.9 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-aspartate catabolism bztD med BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 60% 84% 261.9 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
D-alanine catabolism Pf6N2E2_5405 med ABC transporter for D-Alanine, ATPase component (characterized) 58% 90% 260.8 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-histidine catabolism bgtA med BgtA aka SLR1735, component of Arginine/lysine/histidine/glutamine porter (characterized) 56% 91% 247.3 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-asparagine catabolism peb1C med PEB1C, component of Uptake system for glutamate and aspartate (characterized) 52% 99% 246.9 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-aspartate catabolism peb1C med PEB1C, component of Uptake system for glutamate and aspartate (characterized) 52% 99% 246.9 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-histidine catabolism BPHYT_RS24015 med ABC transporter related (characterized, see rationale) 51% 94% 243.8 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-histidine catabolism hisP med Probable ATP-binding component of ABC transporter, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) 50% 93% 234.2 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-citrulline catabolism AO353_03040 med ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized) 49% 97% 227.3 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
D-glucosamine (chitosamine) catabolism AO353_21725 med ABC transporter for D-glucosamine, ATPase component (characterized) 48% 89% 223.8 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-citrulline catabolism PS417_17605 med 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) 50% 87% 213.8 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-histidine catabolism PA5503 med Methionine import ATP-binding protein MetN 2, component of L-Histidine uptake porter, MetIQN (characterized) 41% 72% 183.3 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-proline catabolism proV lo glycine betaine/l-proline transport atp-binding protein prov (characterized) 41% 56% 167.5 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
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) 42% 58% 164.9 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-histidine catabolism hutV lo ABC transporter for L-Histidine, ATPase component (characterized) 39% 87% 155.6 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
D-maltose catabolism thuK lo Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized) 36% 64% 148.7 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
trehalose catabolism thuK lo Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized) 36% 64% 148.7 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-arabinose catabolism xacJ lo Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) 39% 62% 148.3 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-tryptophan catabolism ecfA1 lo Energy-coupling factor transporter ATP-binding protein EcfA1; Short=ECF transporter A component EcfA; EC 7.-.-.- (characterized, see rationale) 40% 78% 141.7 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
2'-deoxyinosine catabolism nupA lo Purine/cytidine ABC transporter ATP-binding protein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized) 32% 51% 127.9 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2
L-arabinose catabolism xylGsa lo Xylose/arabinose import ATP-binding protein XylG; EC 7.5.2.13 (characterized, see rationale) 31% 94% 125.6 Glutamine transport ATP-binding protein GlnQ; EC 7.4.2.- 62% 291.2

Sequence Analysis Tools

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Sequence

MIKTVDLKKIFTGRGTEVRAVDGVTTHIKSGEVVVVIGPSGSGKSTYLRCLNGLETLTDG
HIMIDGIDLADKKTDLNKVRREVGMVFQQFNLFPHKTVLDNIILAQQVVRKRNRKEAEDK
ARQLLKKVGIADKESVYPGHLSGGQQQRVAIARALAMDPKIMLFDEPTSALDPEMVGEVL
DVMKQLAREGMTMVVVTHEMGFAREVADRVIFMDHGKLVEEGTPEHFFTEPREERAKDFL
RQVL

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