GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Escherichia coli BW25113

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 16645 b2546 predicted sugar transporter subunit: membrane component of ABC superfamily (NCBI)

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__Keio:16645
          Length = 332

 Score =  201 bits (511), Expect = 2e-56
 Identities = 124/325 (38%), Positives = 187/325 (57%), Gaps = 12/325 (3%)

Query: 1   MTAPSSPAPLATDKPRFDLLAFARKHRTILFLLLLVA----VFGAANERFLTARNALNIL 56
           M+A S P P         L  F  +H   + LL+++A    VF      F++  N +N+L
Sbjct: 1   MSASSLPLPQGKS---VSLKQFVSRHINEIGLLVVIAILYLVFSLNAPGFISLNNQMNVL 57

Query: 57  SEVSIYGIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIALLVST 116
            + +  GI A  MT +I+ G IDV+VG ++AF S+  A+++   V    A  L+ LL+  
Sbjct: 58  RDAATIGIAAWAMTLIIISGEIDVSVGPMVAFVSVCLAFLLQFEVPLAVAC-LLVLLLGA 116

Query: 117 LIGLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWWGSGEI 176
           L+G   G ++G      +VP+F+ TLG  +  RG  L + +  P+    +    W  G+ 
Sbjct: 117 LMGTLAGVLRGV----FNVPSFVATLGLWSALRGMGLFMTNALPVPIDENEVLDWLGGQF 172

Query: 177 LFLPVPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGA 236
           L +PV  +I  ++ A      R T +GR V+AVGGNA AA+L G+NV  +   ++ + G 
Sbjct: 173 LGVPVSALIMIVLFALFVFISRKTAFGRSVFAVGGNATAAQLCGINVRRVRILIFTLSGL 232

Query: 237 LAGLSGFLLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLS 296
           LA ++G LL+ARLGS  A A  G E  VIA+VV+GG +L+GG G + GT+LG L+I ++ 
Sbjct: 233 LAAVTGILLAARLGSGNAGAANGLEFDVIAAVVVGGTALSGGRGSLFGTLLGVLVITLIG 292

Query: 297 NGLVMLHVTSYVQQVVIGLIIVAAV 321
           NGLV+L + S+ QQVV G+IIV AV
Sbjct: 293 NGLVLLGINSFFQQVVRGVIIVVAV 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: 253
Number of extensions: 14
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: 332
Length adjustment: 28
Effective length of query: 304
Effective length of database: 304
Effective search space:    92416
Effective search space used:    92416
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