GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16925 in Echinicola vietnamensis KMM 6221, DSM 17526

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

Query= uniprot:B2SYR4
         (338 letters)



>FitnessBrowser__Cola:Echvi_1280
          Length = 318

 Score =  187 bits (476), Expect = 2e-52
 Identities = 101/313 (32%), Positives = 176/313 (56%), Gaps = 11/313 (3%)

Query: 33  ITEYSLIVIFVVMFATMSLTVDHFFSIENMLGLALSISQIGMVSCTMMFCLASRDFDLSV 92
           I ++  ++  +++   +SL  D F ++ N   +   +S    +S  M   + +   DLSV
Sbjct: 4   IAKFQSLIALIILCLVLSLLSDRFLTLANGWNVMRQVSVNICISVGMTLVILTAGIDLSV 63

Query: 93  GSTVAFAGVLCA-MVLNATG----NTFI------AIVAAVAAGGVIGFVNGAVIAYLRIN 141
           GS +A  G + A ++ N       N  I      A++  V  G  +G+ NG  I   ++ 
Sbjct: 64  GSILALCGAVTASLIKNGIAVEGLNLHIGFAPLGAVILGVGLGFGLGWFNGWTITRFKVP 123

Query: 142 ALITTLATMEIVRGLGFIVSHGQAVGVSSDTFIALGGLSFFGVSLPIWVTLLCFIVFGVM 201
             + TLA + I RGL  + + G  +    + F  LG   F G+ +P+W+T +   +  ++
Sbjct: 124 PFVATLAMLTIARGLTMLWTGGFPINGLGEDFAFLGTGWFLGIPMPVWITAVIVALAVLL 183

Query: 202 LNQTVYGRNTLAIGGNPEASRLAGINVERTRVYIFLIQGAVTALAGVILASRITSGQPNA 261
             +T +GR   AIGGN  A+RL+GIN+ R ++ ++ I G + A+ G+I+ SR+ S QPNA
Sbjct: 184 TKKTKFGRYVYAIGGNERAARLSGINISRVKMTVYAIAGGLAAVGGMIVTSRLDSAQPNA 243

Query: 262 AQGFELNVISACVLGGVSLLGGRATISGVVIGVLIMGTVENVMNLMNIDAFYQYLVRGAI 321
              +EL+ I+A V+GG SL GG+ TI G V+G +I+G + N + L+N+  F+Q +V+GA+
Sbjct: 244 GISYELDAIAAVVIGGTSLSGGKGTIMGAVLGGIIIGVLNNGLVLLNVSPFWQQVVKGAV 303

Query: 322 LLAAVLLDQLKNR 334
           +L AV++D+  ++
Sbjct: 304 ILLAVVIDKANSK 316


Lambda     K      H
   0.326    0.139    0.396 

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: 310
Number of extensions: 20
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: 338
Length of database: 318
Length adjustment: 28
Effective length of query: 310
Effective length of database: 290
Effective search space:    89900
Effective search space used:    89900
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 (21.7 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