GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Dinoroseobacter shibae DFL-12

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate 3608017 Dshi_1424 inner-membrane translocator (RefSeq)

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__Dino:3608017
          Length = 343

 Score =  130 bits (326), Expect = 7e-35
 Identities = 102/337 (30%), Positives = 159/337 (47%), Gaps = 24/337 (7%)

Query: 10  FGAAQAGAQSQLALPASRGKRARSELARLRELALLPALALLIVIGAFISPSFLTKANLIS 69
           F  A  GA +     + R KR R+E   L   +LL  L  L    + +   F +  N+ S
Sbjct: 5   FPTADTGAHAM----SRRPKRLRAEHRGLVLGSLL--LVALFTAASILVEGFASANNIRS 58

Query: 70  VLGASAALALVVLAESLIVLTGKFDLSLESTVGIAPAVGAMLVMPAASAGFGMQWPAAAG 129
           +L  +A L L  L ++++   G  DLS+   +G +  + A L        FG   PA   
Sbjct: 59  ILLLAAFLGLAALGQTMVATVGGLDLSIPFVIGASNILLAYL--------FGTSLPAPLA 110

Query: 130 LLAIVVVGAVIGFINGFLVVRLRLNAFIVTLAMLIVLRG-----MLVGATKGGTLFDMPT 184
           +L I+ +GA+IG +NG +  R++  A I+TL +   + G       +G+   GT+F    
Sbjct: 111 ILCILAMGALIGVLNGVMSYRIQGQALILTLGVGFAVVGGAQIFTSLGSQFSGTVFSQVP 170

Query: 185 SFFA-----LATTIVLGLPLSVWLAAAAFAIAAFMLRYHRLGRALYAIGGNPEAARAAGI 239
            +F+       TT  L LP  + + AA  A   F +   R GRA+YAIGGN  AA    I
Sbjct: 171 GWFSNIASISGTTFGLKLPPVILIWAAIAASLIFWINRTRAGRAIYAIGGNRTAAARLRI 230

Query: 240 RVERITWGVFVLGSILASVGGLIVTGYVGAINANQGNGMIFTVFAAAVIGGISLDGGKGT 299
              R+    + +  + A+  G ++ G+ G      G+  +FT  AA V+GG SL GG G 
Sbjct: 231 SEFRVWVSTYTISGLTAAATGCLLLGFSGGGFVGVGDPYLFTTVAAVVVGGTSLLGGTGG 290

Query: 300 MFGALTGVLLLGVVQNLLTLAQVPSFWIQAIYGAIIL 336
               + GVL+L V+ + L    +     Q ++G +IL
Sbjct: 291 YGATVIGVLVLQVLTSFLVGMGLDYAAQQTVFGLLIL 327


Lambda     K      H
   0.326    0.140    0.397 

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: 293
Number of extensions: 16
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: 351
Length of database: 343
Length adjustment: 29
Effective length of query: 322
Effective length of database: 314
Effective search space:   101108
Effective search space used:   101108
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 (21.6 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