GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Pseudomonas simiae WCS417

Align Inositol ABC transport system, permease protein IatP, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate GFF2365 PS417_12060 sugar ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__WCS417:GFF2365
          Length = 325

 Score =  264 bits (674), Expect = 3e-75
 Identities = 158/324 (48%), Positives = 205/324 (63%), Gaps = 6/324 (1%)

Query: 1   MTAPSSPAPLATDKPRFDLLAFARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVS 60
           M A +  AP+ T  PR  L     +    L  +LL  V   ++E F+T RN ++IL + S
Sbjct: 1   MNAKTITAPV-TAAPRNRLRLSLDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTS 59

Query: 61  IYGIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIALLVSTLIGL 120
           I GI+AVGMT+VIL  GID++VGS+LAFA + +A V T   G      L A+      G 
Sbjct: 60  INGILAVGMTYVILTKGIDLSVGSILAFAGLCSAMVATQGYG-----LLAAVSAGMFAGA 114

Query: 121 AGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWWGSGEILFLP 180
             G V G  V  L +P F+ TLG +++ RG T +LNDG PI+   DAY   G G+I  + 
Sbjct: 115 MLGVVNGFMVANLSIPPFVATLGMLSIARGMTFILNDGSPITDLPDAYLALGIGKIGPIG 174

Query: 181 VPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGL 240
           VP++IFA+VA    + LRYT YGR VYAVGGN ++AR SG+ V  +  SVY + G LAGL
Sbjct: 175 VPIIIFAVVALIFWMVLRYTTYGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSGLLAGL 234

Query: 241 SGFLLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLV 300
           +G +LSAR  SA   AG  YEL  IA+VVIGG SL+GG+G + GT+ GALLIGV++NGL 
Sbjct: 235 AGVVLSARTTSALPQAGVSYELDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVINNGLN 294

Query: 301 MLHVTSYVQQVVIGLIIVAAVAFD 324
           +L V+SY QQV  GLIIV AV  D
Sbjct: 295 LLGVSSYYQQVAKGLIIVFAVLID 318


Lambda     K      H
   0.325    0.140    0.413 

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: 290
Number of extensions: 12
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: 332
Length of database: 325
Length adjustment: 28
Effective length of query: 304
Effective length of database: 297
Effective search space:    90288
Effective search space used:    90288
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 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