GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gguB in Echinicola vietnamensis KMM 6221, DSM 17526

Align GguB aka ATU2346 aka AGR_C_4262, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate Echvi_1280 Echvi_1280 Ribose/xylose/arabinose/galactoside ABC-type transport systems, permease components

Query= TCDB::O05177
         (398 letters)



>FitnessBrowser__Cola:Echvi_1280
          Length = 318

 Score =  163 bits (412), Expect = 7e-45
 Identities = 121/376 (32%), Positives = 182/376 (48%), Gaps = 62/376 (16%)

Query: 23  NIREYGMLIALVAIMVFFQFYTGGILFRPVNLTNLILQNSFIVIMALGMLLVIVAGHIDL 82
           +I ++  LIAL+ + +     +   L    N  N++ Q S  + +++GM LVI+   IDL
Sbjct: 3   SIAKFQSLIALIILCLVLSLLSDRFLTL-ANGWNVMRQVSVNICISVGMTLVILTAGIDL 61

Query: 83  SVGSIVAFVGAIAAILTVQWGMNPFLAALICLVIGGIIGAAQGYWIAYHRIPSFIVTLAG 142
           SVGSI+A  GA+ A L                                         +  
Sbjct: 62  SVGSILALCGAVTASL-----------------------------------------IKN 80

Query: 143 MLVFRGLTLFVLGGKNIGPFPTDFQVISTGFLPDIGGIEGLNTTSMILTVLI-TVALFYL 201
            +   GL L      +IG  P    ++  G    +G   G   T   +   + T+A+  +
Sbjct: 81  GIAVEGLNL------HIGFAPLGAVILGVGLGFGLGWFNGWTITRFKVPPFVATLAMLTI 134

Query: 202 AWRRRVVNVKHGIDVEPFGFFIVQNLLISGAILFLGYQLSTYRGLPNVLIVMLVLIALYS 261
           A          G+ +   G F +  L    A L  G+ L    G+P  + +  V++AL  
Sbjct: 135 A---------RGLTMLWTGGFPINGLGEDFAFLGTGWFL----GIPMPVWITAVIVALAV 181

Query: 262 FVTRRTTIGRRVYAMGGNEKATKLSGINTERLSFLTFVNMGVLAGLAGMIIATRLNSATP 321
            +T++T  GR VYA+GGNE+A +LSGIN  R+    +   G LA + GMI+ +RL+SA P
Sbjct: 182 LLTKKTKFGRYVYAIGGNERAARLSGINISRVKMTVYAIAGGLAAVGGMIVTSRLDSAQP 241

Query: 322 KAGVGFELDVIAACFIGGASASGGVGKITGAVIGAFIMGVMNNGMSIVGLGIDFQQMVKG 381
            AG+ +ELD IAA  IGG S SGG G I GAV+G  I+GV+NNG+ ++ +   +QQ+VKG
Sbjct: 242 NAGISYELDAIAAVVIGGTSLSGGKGTIMGAVLGGIIIGVLNNGLVLLNVSPFWQQVVKG 301

Query: 382 LVLLAAVFFDVYNKNK 397
            V+L AV  D  N  +
Sbjct: 302 AVILLAVVIDKANSKE 317


Lambda     K      H
   0.329    0.145    0.422 

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: 477
Number of extensions: 24
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 398
Length of database: 318
Length adjustment: 29
Effective length of query: 369
Effective length of database: 289
Effective search space:   106641
Effective search space used:   106641
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.

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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