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 GFF2674 PS417_13640 ribose ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__WCS417:GFF2674
          Length = 325

 Score =  210 bits (535), Expect = 3e-59
 Identities = 123/299 (41%), Positives = 178/299 (59%), Gaps = 6/299 (2%)

Query: 32  LLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVILIGGIDVAVGSLLAFASI 91
           L+LL+  F  A+E FLT +N   I  + S+  ++A GMTFVIL  GID++VG++LA    
Sbjct: 28  LILLLVGFALASENFLTMQNLSIISQQASVNVVLAAGMTFVILTAGIDLSVGAILA---- 83

Query: 92  AAAYVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGA 151
            A+ VV       P   +  +      GL  G V G  + ++ +P FIVTLG +T  RG 
Sbjct: 84  -ASAVVALQASMSPQFGMFGIAAGIGFGLLLGLVNGGLIAFMRLPPFIVTLGALTAMRGL 142

Query: 152 TLLLNDGGPISGFNDAYRWWGSGEILFLPVPVVIFALVAAAGHVALRYTRYGRQVYAVGG 211
             LL D   +   +  + + G+  +L +P  V+I   V A     LR T  G Q+Y+VGG
Sbjct: 143 ARLLADDKTVFNPDLPFAFIGNDSLLGVPWLVIIAVAVVALSWFILRRTVMGVQIYSVGG 202

Query: 212 NAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGSAEAV-AGTGYELRVIASVVI 270
           N EAARLSG+ V  +   VYA+ GALAGL   + ++RL +A  +  G  YEL  IA+V++
Sbjct: 203 NPEAARLSGIKVWKVLLFVYAMSGALAGLGAVMSASRLFAANGLQLGQSYELDAIAAVIL 262

Query: 271 GGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQVVIGLIIVAAVAFDHYART 329
           GG S TGG G +GGT++GAL+I VL+NGLV+L V+   Q ++ G++I+ AVA D Y ++
Sbjct: 263 GGTSFTGGVGTIGGTLIGALIIAVLTNGLVLLGVSDIWQYIIKGIVIIGAVALDRYRQS 321


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: 256
Number of extensions: 15
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: 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