GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HMIT in Klebsiella michiganensis M5al

Align Proton myo-inositol cotransporter; H(+)-myo-inositol cotransporter; Hmit; H(+)-myo-inositol symporter; Solute carrier family 2 member 13 (characterized)
to candidate BWI76_RS03110 BWI76_RS03110 MFS transporter

Query= SwissProt::Q96QE2
         (648 letters)



>FitnessBrowser__Koxy:BWI76_RS03110
          Length = 499

 Score =  228 bits (580), Expect = 6e-64
 Identities = 128/349 (36%), Positives = 201/349 (57%), Gaps = 10/349 (2%)

Query: 76  ETPA--FVYVVAVFSALGGFLFGYDTGVVSGAMLLLKRQLSLDALWQELLVSSTVGAAAV 133
           ETP   FV VVA+ + LGG LFGYDTGV+SGA+L +  +L L      L+ SS +  AA 
Sbjct: 18  ETPTTPFVKVVALIATLGGLLFGYDTGVISGALLFMGTELHLTPFTTGLVTSSLLFGAAF 77

Query: 134 SALAGGALNGVFGRRAAILLASALFTAGSAVLAAANNKETLLAGRLVVGLGIGIASMTVP 193
            AL  G L    GR+  IL  + LF  G+   + A +   ++  RL++G+ +G A+ TVP
Sbjct: 78  GALLSGNLANAAGRKKIILWLAVLFAIGAIGTSMAPDVNWMIFFRLILGVAVGGAAATVP 137

Query: 194 VYIAEVSPPNLRGRLVTINTLFITGGQFFASVVDGAFSYL--QKDGWRYMLGLAAVPAVI 251
           VYIAE++P N RG+LVT+  L I  GQ  A + +  F  +   +  WR+ML +A +PAV+
Sbjct: 138 VYIAEIAPANKRGQLVTLQELMIVSGQLLAYISNATFHEVWGGESTWRWMLAVATLPAVL 197

Query: 252 QFFGFLFLPESPRWLIQKGQTQKARRILSQMRGNQTIDEEYDSIKNNIEEEEKEVGSAGP 311
            +FG +F+P+SPRW   KG+  +ARR+L + R    ++ E   I   ++E+     + G 
Sbjct: 198 LWFGMMFMPDSPRWYAMKGRLAEARRVLERTRHKDDVEWELLEITETLDEQR----NLGK 253

Query: 312 VICRMLSYPPTRRALIVGCGLQMFQQLSGINTIMYYSATILQMSGVEDDRLAIWLASVTA 371
                +  P   +  ++G G+ + QQL+G+NTIMYY+ T+L   G+ D+  A++      
Sbjct: 254 PRFSEIMTPWLFKLFMIGIGIAVIQQLTGVNTIMYYAPTVLTSVGMTDN-AALFATIANG 312

Query: 372 FTNFIFTLVGVWLVEKVGRRKLTFGSLAGTTVALIIL-ALGFVLSAQVS 419
             + + T VG+W++ K+GRR +T     G T  L+ + A+ ++L   V+
Sbjct: 313 VVSVLMTFVGIWMLGKIGRRPMTMIGQFGCTACLVFIGAVSYLLPETVN 361


Lambda     K      H
   0.321    0.136    0.410 

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: 744
Number of extensions: 46
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 2
Length of query: 648
Length of database: 499
Length adjustment: 36
Effective length of query: 612
Effective length of database: 463
Effective search space:   283356
Effective search space used:   283356
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 53 (25.0 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