GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Echinicola vietnamensis KMM 6221, DSM 17526

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate Echvi_1280 Echvi_1280 Ribose/xylose/arabinose/galactoside ABC-type transport systems, permease components

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__Cola:Echvi_1280
          Length = 318

 Score =  182 bits (461), Expect = 1e-50
 Identities = 108/309 (34%), Positives = 170/309 (55%), Gaps = 5/309 (1%)

Query: 44  LPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAESLIVLTGKFDLSLESTVGI 103
           L AL +L ++ + +S  FLT AN  +V+   +    + +  +L++LT   DLS+ S + +
Sbjct: 10  LIALIILCLVLSLLSDRFLTLANGWNVMRQVSVNICISVGMTLVILTAGIDLSVGSILAL 69

Query: 104 APAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGF----INGFLVVRLRLNAFIVT 159
             AV A L+    +   G+        L  V++G  +GF     NG+ + R ++  F+ T
Sbjct: 70  CGAVTASLIKNGIAVE-GLNLHIGFAPLGAVILGVGLGFGLGWFNGWTITRFKVPPFVAT 128

Query: 160 LAMLIVLRGMLVGATKGGTLFDMPTSFFALATTIVLGLPLSVWLAAAAFAIAAFMLRYHR 219
           LAML + RG+ +  T G  +  +   F  L T   LG+P+ VW+ A   A+A  + +  +
Sbjct: 129 LAMLTIARGLTMLWTGGFPINGLGEDFAFLGTGWFLGIPMPVWITAVIVALAVLLTKKTK 188

Query: 220 LGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYVGAINANQGNGMI 279
            GR +YAIGGN  AAR +GI + R+   V+ +   LA+VGG+IVT  + +   N G    
Sbjct: 189 FGRYVYAIGGNERAARLSGINISRVKMTVYAIAGGLAAVGGMIVTSRLDSAQPNAGISYE 248

Query: 280 FTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFWIQAIYGAIILGSL 339
               AA VIGG SL GGKGT+ GA+ G +++GV+ N L L  V  FW Q + GA+IL ++
Sbjct: 249 LDAIAAVVIGGTSLSGGKGTIMGAVLGGIIIGVLNNGLVLLNVSPFWQQVVKGAVILLAV 308

Query: 340 MVARLASGE 348
           ++ +  S E
Sbjct: 309 VIDKANSKE 317


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: 294
Number of extensions: 17
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: 318
Length adjustment: 28
Effective length of query: 323
Effective length of database: 290
Effective search space:    93670
Effective search space used:    93670
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