GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Shewanella sp. ANA-3

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 7024901 Shewana3_2075 inner-membrane translocator (RefSeq)

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__ANA3:7024901
          Length = 405

 Score =  127 bits (318), Expect = 6e-34
 Identities = 86/271 (31%), Positives = 146/271 (53%), Gaps = 7/271 (2%)

Query: 53  LNILSEVSIYGIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIAL 112
           ++IL+  +   ++++GM+ VI  GGID++VG+++A A    A ++       P   L+ +
Sbjct: 98  IDILNRSAPVALLSIGMSLVIATGGIDLSVGAVMAIAGAVCANLLLV-----PDISLVTV 152

Query: 113 LVSTLI-GLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWW 171
           + + LI GL  G + G  V++L +   + TL  M   RG   L+N G  I+  +  +   
Sbjct: 153 IAAGLIVGLLAGCINGGLVSFLGIQPIVATLLLMVAGRGVAQLINQGQIITFQHPGFAAI 212

Query: 172 GSGEILFLPVPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVY 231
           G G+ L LP+PV I   +     + LR T  G  + AVG NA+A+R  G+N   I    Y
Sbjct: 213 GVGQFLGLPMPVWIVIGMLTFSQLLLRKTALGLFIEAVGCNAKASRYLGINDKSIKLFAY 272

Query: 232 AIIGALAGLSGFLLSARL-GSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGAL 290
            I G  A L+G + +A + GS    AG   EL  + +VVIGGA+LTGG   +  +V+GAL
Sbjct: 273 GIAGLCAALAGMISTADIQGSDANNAGLWLELDAVLAVVIGGAALTGGRFSLILSVVGAL 332

Query: 291 LIGVLSNGLVMLHVTSYVQQVVIGLIIVAAV 321
           +I  L+  +++  + +    ++  ++I+  +
Sbjct: 333 IIQTLATTIIVSGLPAKFNLLIKAIVILTVL 363


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: 248
Number of extensions: 15
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: 405
Length adjustment: 30
Effective length of query: 302
Effective length of database: 375
Effective search space:   113250
Effective search space used:   113250
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.

Links

Downloads

Related tools

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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