GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Dinoroseobacter shibae DFL-12

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 3609042 Dshi_2431 Monosaccharide-transporting ATPase (RefSeq)

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__Dino:3609042
          Length = 328

 Score =  168 bits (426), Expect = 1e-46
 Identities = 100/297 (33%), Positives = 167/297 (56%), Gaps = 9/297 (3%)

Query: 30  LFLLLLVAVFGA---ANERFLTARNALNILSEVSIYGIIAVGMTFVILIGGIDVAVGSLL 86
           L LL+ + +F A   A+  FL A N  +     +   +IA  M  +I+ G ID++V S++
Sbjct: 26  LLLLVAIGIFVANSFASPYFLNAWNLSDATFNFTEKAMIAFAMALLIISGEIDLSVASII 85

Query: 87  AFASIAAAYVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHVPAFIVTLGGMT 146
           A AS A    V   VG  P   LI L V    GL  G   G  VT + +P+ +VT+G M+
Sbjct: 86  ALASTAMGAAVQMGVGT-PGLVLIGLGV----GLLCGAFNGVLVTRMGLPSIVVTIGTMS 140

Query: 147 VWRGATLLLNDGGPISGFNDAYRWWGSGEILF-LPVPVVIFALVAAAGHVALRYTRYGRQ 205
           ++RG + ++       G+ +++ W+G G + + +   +V+FA++A    + L  T +GR 
Sbjct: 141 LFRGISYIVLGDQAFRGYPESFSWFGQGYVWWVISFELVLFAIIAVIYAMLLHKTNFGRA 200

Query: 206 VYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGSAEAVAGTGYELRVI 265
           VYA+G NA  A  SG+ V  +   ++ + G ++G++   L+ARLGS       G+EL V+
Sbjct: 201 VYAIGNNATGAMFSGIRVQRVKFILFLLTGLMSGVAAICLTARLGSTRPSIAMGWELEVV 260

Query: 266 ASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQVVIGLIIVAAVA 322
             VV+GG S+ GGSG + G V+ A ++G+++ GL +L+V   V  +VIG +++  +A
Sbjct: 261 TMVVLGGVSILGGSGTILGVVIAAFVMGLVTFGLGLLNVPGIVMSIVIGALLIGVIA 317


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: 262
Number of extensions: 16
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: 328
Length adjustment: 28
Effective length of query: 304
Effective length of database: 300
Effective search space:    91200
Effective search space used:    91200
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