GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Phaeobacter inhibens BS107

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 GFF2762 PGA1_c28050 putative sugar transport system, permease protein

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__Phaeo:GFF2762
          Length = 353

 Score =  150 bits (380), Expect = 3e-41
 Identities = 105/316 (33%), Positives = 162/316 (51%), Gaps = 27/316 (8%)

Query: 29  ILFLLLLVAVFGAA-NERFLTARNALNILSEVSIYGIIAVGMTFVILIGGIDVAVGSLLA 87
           ++ L+L V VFG     +F +      IL +V I GI+A   + VIL  GID++VG+++ 
Sbjct: 45  LIVLVLSVIVFGLLLGSKFFSPFALTLILQQVGIVGIVACAQSLVILTAGIDLSVGAIMV 104

Query: 88  FASIAAAYVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHVPAFIVTLGGMTV 147
            +S+      T   G  P    +A+    + G   G++ G  V  + +P FIVTLG   +
Sbjct: 105 LSSVVMGQF-TFRYGLPPE---VAVACGLICGTICGFINGWLVARMKLPPFIVTLGMWQI 160

Query: 148 WRGATLLLNDGGPISG------------FNDAYRWWGSG---EILFLPVPVVIFALVAAA 192
              +  L +    I              F +  +  G+     ++F+ + VV+ A V   
Sbjct: 161 VLASNFLYSANETIRSQTIAAEAPLLQLFGEKIKIGGAVFTYGVIFMVILVVLLAYV--- 217

Query: 193 GHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGSA 252
               LR+T +GR VYAVG + EAA LSGV V  +  SVY + G +   +G+ +  R+GS 
Sbjct: 218 ----LRHTAWGRHVYAVGDDPEAAELSGVKVTRVLISVYMLSGLICAFAGWAMIGRIGSV 273

Query: 253 EAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQVV 312
              +G    +  I +VVIGG SL GG G + GT  GAL++GV + GL +L   +    ++
Sbjct: 274 SPTSGQLANIESITAVVIGGISLFGGRGSILGTFFGALIVGVFTLGLRLLGADAQWTYLL 333

Query: 313 IGLIIVAAVAFDHYAR 328
           IGL+I+AAVA D + R
Sbjct: 334 IGLLIIAAVAVDQWIR 349


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: 246
Number of extensions: 11
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: 332
Length of database: 353
Length adjustment: 29
Effective length of query: 303
Effective length of database: 324
Effective search space:    98172
Effective search space used:    98172
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