GapMind for catabolism of small carbon sources

 

Protein WP_011384270.1 in Magnetospirillum magneticum AMB-1

Annotation: NCBI__GCF_000009985.1:WP_011384270.1

Length: 262 amino acids

Source: GCF_000009985.1 in NCBI

Candidate for 18 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-histidine catabolism Ac3H11_2560 med ABC transporter for L-Histidine, ATPase component (characterized) 44% 89% 185.3 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
putrescine catabolism potA lo PotG aka B0855, component of Putrescine porter (characterized) 40% 58% 147.1 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
L-histidine catabolism hutV lo ABC transporter for L-Histidine, ATPase component (characterized) 40% 78% 146.7 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
D-maltose catabolism aglK lo ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 40% 54% 141 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
D-maltose catabolism thuK lo ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 40% 54% 141 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
sucrose catabolism aglK lo ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 40% 54% 141 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
trehalose catabolism aglK lo ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 40% 54% 141 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
trehalose catabolism malK lo MsmK aka SMU.882, component of The raffinose/stachyose transporter, MsmEFGK (MalK (3.A.1.1.27) can probably substitute for MsmK; Webb et al., 2008). This system may also transport melibiose, isomaltotriose and sucrose as well as isomaltosaccharides (characterized) 38% 53% 140.6 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
D-maltose catabolism musK lo ABC-type maltose transporter (EC 7.5.2.1) (characterized) 35% 66% 137.5 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
sucrose catabolism thuK lo ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) 39% 56% 130.6 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
xylitol catabolism Dshi_0546 lo ABC transporter for Xylitol, ATPase component (characterized) 34% 68% 129.4 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
D-cellobiose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 35% 66% 124.8 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
D-glucose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 35% 66% 124.8 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
lactose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 35% 66% 124.8 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
D-maltose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 35% 66% 124.8 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
sucrose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 35% 66% 124.8 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
trehalose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 35% 66% 124.8 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4
D-cellobiose catabolism TM0027 lo TM0027, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized) 32% 76% 109 Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 45% 201.4

Sequence Analysis Tools

View WP_011384270.1 at NCBI

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

Find the best match in UniProt

Compare to protein structures

Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

Find homologs in fast.genomics

Fitness BLAST: loading...

Sequence

MDALAPVSPPVIRLEGLAFGYPGDRSHAIVLQDLDLEVRHGDFIALVGQSGAGKSTLLRV
IAGLVPAVLGQVYVEPPKEPDSRQIGMVFQDARLLPWRRVLANVEYGLEGLVKSRHERRR
RALAALDLVGLTEFADRWPHHLSGGQRQRVGLARALAVRPALLLMDEPFGALDPATRHGL
QDQLLSIWQATGTSIIFVTHDIDEATYLADRVIVLGGSPARILRQLDVEAPRPRCRNDLA
DDPTATALRSQLYETFFYKDGI

This GapMind analysis is from Sep 17 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