GapMind for catabolism of small carbon sources

 

Protein WP_028310092.1 in Derxia gummosa DSM 723

Annotation: NCBI__GCF_000482785.1:WP_028310092.1

Length: 338 amino acids

Source: GCF_000482785.1 in NCBI

Candidate for 19 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
sucrose catabolism thuK med ABC transporter (characterized, see rationale) 40% 92% 242.7 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
xylitol catabolism Dshi_0546 med ABC transporter for Xylitol, ATPase component (characterized) 43% 94% 239.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
L-fucose catabolism SM_b21106 med ABC transporter for L-Fucose, ATPase component (characterized) 40% 97% 237.3 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
N-acetyl-D-glucosamine catabolism SMc02869 med N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 40% 90% 224.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
D-glucosamine (chitosamine) catabolism SMc02869 med N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 40% 90% 224.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
lactose catabolism lacK med LacK, component of Lactose porter (characterized) 40% 89% 220.7 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
D-maltose catabolism aglK med ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 43% 77% 218.4 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
sucrose catabolism aglK med ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 43% 77% 218.4 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
trehalose catabolism aglK med ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 43% 77% 218.4 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
D-sorbitol (glucitol) catabolism mtlK med ABC transporter for D-Sorbitol, ATPase component (characterized) 42% 83% 216.1 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
D-cellobiose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 39% 97% 232.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
D-glucose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 39% 97% 232.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
lactose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 39% 97% 232.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
D-maltose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 39% 97% 232.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
sucrose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 39% 97% 232.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
trehalose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 39% 97% 232.6 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
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) 38% 97% 229.9 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
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) 37% 98% 219.9 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6
L-histidine catabolism hutV lo ABC transporter for L-Histidine, ATPase component (characterized) 35% 90% 156 Uncharacterized ABC transporter ATP-binding protein YdcT 47% 269.6

Sequence Analysis Tools

View WP_028310092.1 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

MRSASDIELVKVSKLYGGSTRAVDAIDLRIAAGSYCCLLGPSGCGKTSTLRMIAGHEEAS
DGDIIIGGHNVTLLPPSERGTAMMFQSYALFPHMSAIDNVAYSLKVRGQDKVTRRKRAAE
VLELVSMTPYAERKPAQLSGGQQQRVALARALVNEPRVLLLDEPLSALDPFLRVKMRAEL
KRWQKDLGITFVHVTHSQEEAMALSDLAVVMSHGRIEQAGSPHDIFNRPRTEFVARFLGG
HNVIRADAGRPAPIAVRADKVKLAAGAPATAGFDGSSIAGLVRGVEYQGVHVLVTLDAAG
DQELVAMVDEASYYAAPLQPGEACTLSWNSADAHLLAA

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