GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Marinobacter adhaerens HP15

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate GFF2209 HP15_2163 sugar ABC transporter, ATP-binding protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__Marino:GFF2209
          Length = 366

 Score =  211 bits (537), Expect = 2e-59
 Identities = 125/328 (38%), Positives = 185/328 (56%), Gaps = 15/328 (4%)

Query: 26  IDH----GEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQIFIKDRNVTWEEPKDRGIGMVF 81
           +DH    G    LLG SGCGKST+LN I+GL+  S+G +    + V    P+DR I  VF
Sbjct: 28  LDHVWHKGGAYALLGPSGCGKSTMLNIISGLVQPSEGDVLFDGKRVNELSPRDRNIAQVF 87

Query: 82  QSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEILQIQPLLKRKPSELSGGQRQR 141
           Q   +Y  MTV  NL+F LK  K+P ++I+ RV   +E+L+I+  L +K   L+  ++Q+
Sbjct: 88  QFPVIYDSMTVYDNLAFPLKNNKVPASKIKARVHEIAEVLEIEDKLYKKAKNLTADEKQK 147

Query: 142 VAIGRALVR-DVDVFLFDEPLSNLDAKLRSELRVEIKRLHQSLKNTMIYVTHDQIEALTL 200
           V++GR LVR DV   LFDEPL+ +D +L+ +LR ++K++H+    TM+YVTHDQ+EA T 
Sbjct: 148 VSMGRGLVREDVSAILFDEPLTVIDPQLKWKLRRKLKQIHEQFDITMVYVTHDQLEASTF 207

Query: 201 ADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMNFFRGEVEPKD---GRSFVRA 257
           AD+IAVM  G I Q   P  ++  P + FV  FIGSP MN    +  P+    G + V  
Sbjct: 208 ADKIAVMYGGQIVQFGTPTELFEQPNHTFVGFFIGSPGMNLIEVQRCPRGVCFGSTVVSL 267

Query: 258 GGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDGEPTHQAVVDIEEPMGADNLLW 317
                DV      T ++      +G+RPE V+V      +     V+D+E+ +G   ++ 
Sbjct: 268 ESWQVDVLQRTRSTNIK------IGIRPEFVEVSSVASDDTFEAEVLDVED-LGTYKIVT 320

Query: 318 LTFAGQSMSVRIAGQRRYPPGSTVRLSF 345
           +    + M VR + +     GS V LSF
Sbjct: 321 VQLDHEKMKVRQSEEFAASIGSKVHLSF 348


Lambda     K      H
   0.320    0.137    0.392 

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: 336
Number of extensions: 13
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: 361
Length of database: 366
Length adjustment: 29
Effective length of query: 332
Effective length of database: 337
Effective search space:   111884
Effective search space used:   111884
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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.

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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