GapMind for catabolism of small carbon sources

 

Aligments for a candidate for rhaQ in Dinoroseobacter shibae DFL-12

Align RhaQ (characterized, see rationale)
to candidate 3609042 Dshi_2431 Monosaccharide-transporting ATPase (RefSeq)

Query= uniprot:Q7BSH2
         (337 letters)



>FitnessBrowser__Dino:3609042
          Length = 328

 Score =  466 bits (1200), Expect = e-136
 Identities = 242/315 (76%), Positives = 272/315 (86%), Gaps = 1/315 (0%)

Query: 11  RIIPDRLGTPLRRIAASWEVLLFAVAVLIFVFNSLASPYFLDAWNLSDATFNFTEKAMIA 70
           R+IPDRL +P+ +   SWE LL  VA+ IFV NS ASPYFL+AWNLSDATFNFTEKAMIA
Sbjct: 6   RMIPDRLRSPMEQRLKSWETLLLLVAIGIFVANSFASPYFLNAWNLSDATFNFTEKAMIA 65

Query: 71  FAMALLVISGEIDLSVAAIIALASTAMGAAVQIGIGTPGLVLIGIGTGLACGVFNGVLVS 130
           FAMALL+ISGEIDLSVA+IIALASTAMGAAVQ+G+GTPGLVLIG+G GL CG FNGVLV+
Sbjct: 66  FAMALLIISGEIDLSVASIIALASTAMGAAVQMGVGTPGLVLIGLGVGLLCGAFNGVLVT 125

Query: 131 VLKLPSIVVTIGTMSLFRGISYIVLGDQAYGKYPADFAYFGQGYVVWVFSFEFVLFIVLA 190
            + LPSIVVTIGTMSLFRGISYIVLGDQA+  YP  F++FGQGYV WV SFE VLF ++A
Sbjct: 126 RMGLPSIVVTIGTMSLFRGISYIVLGDQAFRGYPESFSWFGQGYVWWVISFELVLFAIIA 185

Query: 191 VLFAILLHATNFGRQVYAIGNNDFAARFSGIPVERVKSILFLLTGIMSGIAAVCLTSRLG 250
           V++A+LLH TNFGR VYAIGNN   A FSGI V+RVK ILFLLTG+MSG+AA+CLT+RLG
Sbjct: 186 VIYAMLLHKTNFGRAVYAIGNNATGAMFSGIRVQRVKFILFLLTGLMSGVAAICLTARLG 245

Query: 251 STRPSIAQGWELEVVTMVVLGGISILGGFRHDRGVFVIAAFVMGLVTFGLGLLNLPGIVM 310
           STRPSIA GWELEVVTMVVLGG+SILGG     GV VIAAFVMGLVTFGLGLLN+PGIVM
Sbjct: 246 STRPSIAMGWELEVVTMVVLGGVSILGGSGTILGV-VIAAFVMGLVTFGLGLLNVPGIVM 304

Query: 311 SIFIGLLIIVTIAIP 325
           SI IG L+I  IA+P
Sbjct: 305 SIVIGALLIGVIALP 319


Lambda     K      H
   0.330    0.145    0.423 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 494
Number of extensions: 27
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 337
Length of database: 328
Length adjustment: 28
Effective length of query: 309
Effective length of database: 300
Effective search space:    92700
Effective search space used:    92700
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 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