GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ibpA in Escherichia coli BW25113

Align Inositol ABC transporter, periplasmic inositol-binding protein IbpA, 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 18116 b4088 D-allose transporter subunit (NCBI)

Query= TCDB::B8H228
         (326 letters)



>FitnessBrowser__Keio:18116
          Length = 311

 Score =  122 bits (305), Expect = 1e-32
 Identities = 99/299 (33%), Positives = 140/299 (46%), Gaps = 25/299 (8%)

Query: 13  GLAAGLGLGTAALGLMTGCARGGAEAEVVVSFNDLSQPFFVAMRRELEDEAAKLGVKVQV 72
           G   GL L T+A           A AE  V    LS PF+V M++ +EDEA  LGV V +
Sbjct: 10  GTLVGLMLSTSAF----------AAAEYAVVLKTLSNPFWVDMKKGIEDEAKTLGVSVDI 59

Query: 73  L--DAQNNSSKQISDLQAAAVQGAKVVIVAPTDSKALAGAADDLVEQGVAVISVDRNI-- 128
               ++ +   Q+   +  + +  K +  AP  S  L        ++G+ ++++D  I  
Sbjct: 60  FASPSEGDFQSQLQLFEDLSNKNYKGIAFAPLSSVNLVMPVARAWKKGIYLVNLDEKIDM 119

Query: 129 -----AGGKTAVPHVGADNVAGGRAMADWVVKTYPA-GARVVVITNDPGSSSSIERVKGV 182
                AGG      V  DNVA G   A +++    A G  V +I    G++S   R  G 
Sbjct: 120 DNLKKAGGNVEA-FVTTDNVAVGAKGASFIIDKLGAEGGEVAIIEGKAGNASGEARRNGA 178

Query: 183 HDGLAAGGPAFKIVTEQTANSKRDQALTVTQNILTSMRDTPPDVILCLNDDMAMGALEAV 242
            +         K+V  Q A+  R +AL V  N+L   R+     I C ND MAMG  +AV
Sbjct: 179 TEAFKKASQ-IKLVASQPADWDRIKALDVATNVL--QRNPNIKAIYCANDTMAMGVAQAV 235

Query: 243 RAAGLDSAKVKVIGFDAIPEALARIKAGEMVATVEQNPGLQIRTALRQAVDKIKSGAAL 301
             AG  + KV V+G D IPEA   ++AG+M ATV QNP     T L+  VD  KSG  +
Sbjct: 236 ANAG-KTGKVLVVGTDGIPEARKMVEAGQMTATVAQNPADIGATGLKLMVDAEKSGKVI 293


Lambda     K      H
   0.315    0.130    0.353 

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: 219
Number of extensions: 18
Number of successful extensions: 4
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: 326
Length of database: 311
Length adjustment: 27
Effective length of query: 299
Effective length of database: 284
Effective search space:    84916
Effective search space used:    84916
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 48 (23.1 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