GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Klebsiella michiganensis M5al

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 BWI76_RS07245 BWI76_RS07245 ABC transporter

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__Koxy:BWI76_RS07245
          Length = 343

 Score =  211 bits (537), Expect = 2e-59
 Identities = 133/333 (39%), Positives = 198/333 (59%), Gaps = 29/333 (8%)

Query: 12  TDKPRFDLLAFAR-KHR----TILFLLLLV-------AVFGAANERFLTARNALN-ILSE 58
           T+KP F    F + +HR    T +F+++LV       A +   ++ FL   N L  I+ +
Sbjct: 12  TEKPSF----FGQLRHRLPKDTGIFIVMLVIALTFEIAGWYVRDQSFLLNTNRLILIVLQ 67

Query: 59  VSIYGIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDGPA-------TWLIA 111
           V+I GIIAVG+T VI+  GID++ GS++A A++ AA +        P          +I 
Sbjct: 68  VAIIGIIAVGVTQVIITTGIDLSSGSVIALAAVVAASLAQTSDSLSPMFPSLVNMPAIIP 127

Query: 112 LLVSTLIGLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWW 171
           +     +GL  G   G  VT   +P FI TLG M   RG       G PIS  +D++   
Sbjct: 128 IGAGIGVGLLCGLTNGFLVTRTGIPPFIATLGMMVSARGLAQYYTQGNPISFLSDSFTAI 187

Query: 172 GSGEILFLPVPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVY 231
           G G +     PV+IF +VAA  H+AL++TRYG+ VYA+GGN  +A++SG+NV+     VY
Sbjct: 188 GQGAM-----PVIIFFVVAAVFHIALKHTRYGKYVYAIGGNMTSAKVSGINVNKYLVIVY 242

Query: 232 AIIGALAGLSGFLLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALL 291
           AI GAL+GL+G +L+AR+ S ++  G  YEL  IA+ VIGG+SL GG G + GT++GA++
Sbjct: 243 AIAGALSGLAGVVLAARVSSGQSSMGMSYELDAIAAAVIGGSSLMGGVGRITGTLIGAMI 302

Query: 292 IGVLSNGLVMLHVTSYVQQVVIGLIIVAAVAFD 324
           +G++ +G   + V +YVQ ++ G+IIVAAV  D
Sbjct: 303 LGLIKSGFTFVGVDAYVQDIIKGIIIVAAVTID 335


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: 270
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: 343
Length adjustment: 28
Effective length of query: 304
Effective length of database: 315
Effective search space:    95760
Effective search space used:    95760
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