GapMind for catabolism of small carbon sources

 

Aligments 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)



>lcl|FitnessBrowser__Koxy:BWI76_RS03110 BWI76_RS03110 MFS
           transporter
          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.

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