GapMind for catabolism of small carbon sources

 

Protein H281DRAFT_05701 in Paraburkholderia bryophila 376MFSha3.1

Annotation: H281DRAFT_05701 glycerol 3-phosphate ABC transporter ATP-binding protein

Length: 362 amino acids

Source: Burk376 in FitnessBrowser

Candidate for 22 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
D-mannitol catabolism mtlK med MtlK, component of The polyol (mannitol, glucitol (sorbitol), arabitol (arabinitol; lyxitol)) uptake porter, MtlEFGK (characterized) 55% 96% 365.5 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-sorbitol (glucitol) catabolism mtlK med MtlK, component of The polyol (mannitol, glucitol (sorbitol), arabitol (arabinitol; lyxitol)) uptake porter, MtlEFGK (characterized) 55% 96% 365.5 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
L-fucose catabolism SM_b21106 med ABC transporter for L-Fucose, ATPase component (characterized) 53% 99% 356.3 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
lactose catabolism lacK med ABC transporter for Lactose, ATPase component (characterized) 57% 87% 345.9 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-maltose catabolism malK med Maltose-transporting ATPase (EC 3.6.3.19) (characterized) 53% 95% 342.8 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
sucrose catabolism thuK med ABC transporter (characterized, see rationale) 50% 93% 335.9 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-maltose catabolism malK1 med MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized) 49% 99% 334.7 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
trehalose catabolism thuK med MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized) 49% 99% 334.7 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
xylitol catabolism HSERO_RS17020 med ABC-type sugar transport system, ATPase component protein (characterized, see rationale) 50% 90% 332 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-cellobiose catabolism msiK med 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) 49% 100% 329.3 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-maltose catabolism malK_Sm med 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) 48% 100% 327.4 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
trehalose catabolism malK med 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) 48% 100% 327.4 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-glucosamine (chitosamine) catabolism SM_b21216 med ABC transporter for D-Glucosamine, ATPase component (characterized) 49% 99% 322.4 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-maltose catabolism malK_Bb med ABC-type maltose transport, ATP binding protein (characterized, see rationale) 47% 99% 313.2 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
N-acetyl-D-glucosamine catabolism SMc02869 med N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 50% 95% 310.8 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-glucosamine (chitosamine) catabolism SMc02869 med N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 50% 95% 310.8 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-maltose catabolism musK med ABC-type maltose transporter (EC 7.5.2.1) (characterized) 47% 100% 309.3 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
xylitol catabolism Dshi_0546 med ABC transporter for Xylitol, ATPase component (characterized) 46% 100% 308.1 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
L-arabinose catabolism xacK med Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale) 47% 95% 307.8 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
D-galactose catabolism PfGW456L13_1897 med ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized) 47% 95% 305.8 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
trehalose catabolism treV med TreV, component of Trehalose porter (characterized) 47% 76% 234.6 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6
glycerol catabolism glpT lo ABC transporter for Glycerol, ATPase component 2 (characterized) 37% 93% 219.9 sn-glycerol-3-phosphate import ATP-binding protein UgpC; EC 7.6.2.10 65% 452.6

Sequence Analysis Tools

View H281DRAFT_05701 at FitnessBrowser

PaperBLAST (search for papers about homologs of this protein)

Search CDD (the Conserved Domains Database, which includes COG and superfam)

Search PFam (including for weak hits, up to E = 1)

Predict protein localization: PSORTb (Gram negative bacteria)

Predict transmembrane helices and signal peptides: Phobius

Check the SEED with FIGfam search

Fitness BLAST: loading...

Sequence

MAALTLQGVKKTYDGKQFVLHGIDVDVNDGEFVVMVGPSGCGKSTLLRMVAGLERISEGT
ISIAGKVVNELEPKDRNIAMVFQNYALYPHMSVAENMGYALKIAGVDRAQIAQRVNAAAQ
ILELEPLLQRKPRELSGGQRQRVAMGRAIVREPAVFLFDEPLSNLDARLRVQMRLEIQRL
HARLATTSLYVTHDQIEAMTLAQRVIVMNKGHAEQIGAPTEVYERPATVFVAGFIGSPGM
NLLEGRVSDDGSTFDVAGNGPQLPLAGVASIGREVAKGREWTLGIRPEHMSPGQADAPHT
TLTVDSCELLGADNLAHGRWGKHDVTARLPHAHRPAAGEALQVALPARHLHFFDPASGRR
VN

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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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