GapMind for catabolism of small carbon sources

 

Aligments for a candidate for SMc04257 in Dyella japonica UNC79MFTsu3.2

Align ABC transporter for D-Cellobiose and D-Salicin, permease component 1 (characterized)
to candidate N515DRAFT_3133 N515DRAFT_3133 carbohydrate ABC transporter membrane protein 2, CUT1 family (TC 3.A.1.1.-)

Query= reanno::Smeli:SMc04257
         (305 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3133
          Length = 273

 Score =  124 bits (312), Expect = 2e-33
 Identities = 84/281 (29%), Positives = 147/281 (52%), Gaps = 22/281 (7%)

Query: 31  IVYGTLIVVALYYLLPLYVMIVTSLKGMPEIRVGNIFAPPL---EITFEPWVKAWAEACT 87
           +V G LI   L  + PL  M+  S     E    +   PPL     T   + + +  A  
Sbjct: 9   LVNGLLIGSTLVAVFPLLWMLSVSFMRPGE---ASALPPPLLPTHATLANYHELFERA-- 63

Query: 88  GLNCDGLSRGFWNSVRITVPSVIISIAIASVNGYALANWRFKGADLFFTILIVGAFIPYQ 147
                G+ R   NS+ ++    ++S+A   + GYA A  RF G +  F +L+ G  IP Q
Sbjct: 64  -----GMGRYLLNSLGVSSAITLLSLAFNLMAGYAFAKLRFSGRERLFQVLLGGLVIPAQ 118

Query: 148 VMIYPIVIVLREMGVYGTLTGLII--VHTIFGMPILTLLFRNYFAGLPEELFKAARVDGA 205
           V + P+ ++L+ +G+  +   +++  + TIFG+     L R Y  G+P++L +AAR+DGA
Sbjct: 119 VAMLPLFLLLKYLGLVNSYAAVVVPAMATIFGI----FLVRQYARGIPDDLMEAARIDGA 174

Query: 206 GFWTIYFKIMLPMSLPIFVVAMILQVTGIWNDFLFGVV-FTRPEYYPMTVQLNNIVNSVQ 264
           G   I+ +I+LP+  PI V   I      WNDF++ ++  T  E+Y + + L ++  S +
Sbjct: 175 GELRIFVQIVLPLLKPIMVTLAIFTFLTAWNDFMWPLIALTGQEHYTLPIALASL--SRE 232

Query: 265 GVKEYNVNMAATILTGLVPLTVYFVSGRLFVRGIAAGAVKG 305
            V++  + MA +++T L  L ++    R +++G+  G+VKG
Sbjct: 233 HVQDSELMMAGSVVTVLPVLVLFLALQRYYLQGLLLGSVKG 273


Lambda     K      H
   0.329    0.145    0.450 

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: 197
Number of extensions: 10
Number of successful extensions: 2
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: 305
Length of database: 273
Length adjustment: 26
Effective length of query: 279
Effective length of database: 247
Effective search space:    68913
Effective search space used:    68913
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: 48 (23.1 bits)

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 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