GapMind for catabolism of small carbon sources

 

Protein WP_099020204.1 in Marinicella litoralis KMM 3900

Annotation: NCBI__GCF_002591915.1:WP_099020204.1

Length: 228 amino acids

Source: GCF_002591915.1 in NCBI

Candidate for 28 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
sucrose catabolism thuK lo ABC transporter (characterized, see rationale) 34% 56% 134 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
putrescine catabolism potA lo Spermidine/putrescine import ATP-binding protein PotA, component of The spermidine/putrescine uptake porter, PotABCD (characterized) 34% 56% 132.5 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
L-asparagine catabolism peb1C lo PEB1C, component of Uptake system for glutamate and aspartate (characterized) 32% 89% 130.2 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
L-aspartate catabolism peb1C lo PEB1C, component of Uptake system for glutamate and aspartate (characterized) 32% 89% 130.2 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
L-glutamate catabolism gltL lo PEB1C, component of Uptake system for glutamate and aspartate (characterized) 32% 89% 130.2 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-mannitol catabolism mtlK lo ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component (characterized) 36% 57% 129.8 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
L-histidine catabolism BPHYT_RS24015 lo ABC transporter related (characterized, see rationale) 35% 86% 129.4 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-sorbitol (glucitol) catabolism mtlK lo ABC transporter for D-Sorbitol, ATPase component (characterized) 34% 63% 127.1 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
trehalose catabolism thuK lo Trehalose import ATP-binding protein SugC; EC 7.5.2.- (characterized) 31% 54% 126.3 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
N-acetyl-D-glucosamine catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 34% 64% 125.6 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-glucosamine (chitosamine) catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 34% 64% 125.6 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
xylitol catabolism HSERO_RS17020 lo ABC-type sugar transport system, ATPase component protein (characterized, see rationale) 32% 53% 123.2 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
lactose catabolism lacK lo ABC transporter for Lactose, ATPase component (characterized) 32% 55% 122.5 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-cellobiose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 31% 60% 122.1 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-glucose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 31% 60% 122.1 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
lactose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 31% 60% 122.1 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-maltose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 31% 60% 122.1 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
sucrose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 31% 60% 122.1 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
trehalose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 31% 60% 122.1 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
L-fucose catabolism SM_b21106 lo ABC transporter for L-Fucose, ATPase component (characterized) 33% 54% 119.4 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-maltose catabolism malK lo Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized) 32% 55% 115.5 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-cellobiose catabolism msiK lo MsiK protein, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized) 34% 51% 114 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
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% 66% 108.6 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-cellobiose catabolism SMc04256 lo ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) 32% 56% 107.8 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
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) 31% 88% 105.9 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
D-maltose catabolism malK_Sm lo MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized) 30% 53% 104 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
trehalose catabolism malK lo MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized) 30% 53% 104 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7
L-proline catabolism HSERO_RS00900 lo ABC-type branched-chain amino acid transport system, ATPase component protein (characterized, see rationale) 30% 89% 86.3 lipoprotein releasing system, ATP-binding protein; EC 3.6.3.- 53% 237.7

Sequence Analysis Tools

View WP_099020204.1 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

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Sequence

MSDSVVLKCENLSKFFTDGQRKIQIFEGLDFQVKAGESVAIMGASGSGKSTLLHLLGGLD
TANAGDINIQGQQLSKLSGRQRGLLRNQHLGFVYQFHHLLPEFSALENVMMPLLIGKTAK
AAAKQQATEILQQVGLSDRLTHRPAQLSGGERQRAAIARAMVTSPACILADEPTGNLDEK
TASSVMDLLINLKEQLNTSLVLVTHDQKVADKMQHQYLLQQGALIKLS

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