GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Paraburkholderia bryophila 376MFSha3.1

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 H281DRAFT_02714 H281DRAFT_02714 monosaccharide ABC transporter membrane protein, CUT2 family

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__Burk376:H281DRAFT_02714
          Length = 331

 Score =  215 bits (547), Expect = 1e-60
 Identities = 117/303 (38%), Positives = 182/303 (60%), Gaps = 21/303 (6%)

Query: 29  ILFLLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVILIGGIDVAVGSLLAF 88
           +L + LL++VF   +  FLT  N + +    S+  ++++GM  VI+ GGID++VGS++  
Sbjct: 34  LLLVGLLISVF---SPYFLTTNNLMGVFRSFSLIALMSIGMMLVIITGGIDLSVGSVMGL 90

Query: 89  ASIAAA------YVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHVPAFIVTL 142
           +S+  A      Y   A +G G A           +G+A G   G  +TW+ +P FI TL
Sbjct: 91  SSLVTALVFQHGYNAPAAIGAGLA-----------VGIAVGAFNGFMITWIQLPPFIATL 139

Query: 143 GGMTVWRGATLLLNDGGPIS-GFNDAYRWWGSGEILFLPVPVVIFALVAAAGHVALRYTR 201
           G +++ RG   ++  G P++    D++ + G G I F+P PVVI   + A   V +R TR
Sbjct: 140 GTLSIGRGLMYIITKGVPVTPDVPDSFTFIGQGYIGFVPFPVVILLAMTAVFSVVMRQTR 199

Query: 202 YGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGSAEAVAGTGYE 261
           +GR VYA GGN  AARLSGV    +  +VY + G +A ++G +  +R  SAE  +G G E
Sbjct: 200 FGRYVYATGGNEVAARLSGVRTARVKFTVYVLSGLIASMAGVIAFSRFVSAEPASGFGAE 259

Query: 262 LRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQVVIGLIIVAAV 321
           L VIA+  IGGASL+GG+G V G ++GA L G+++NG+V+L++ +Y QQ + G +I+ AV
Sbjct: 260 LDVIAAAAIGGASLSGGAGSVEGAIIGAALAGIITNGVVLLNIDTYAQQAITGCVILIAV 319

Query: 322 AFD 324
           + D
Sbjct: 320 SID 322


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: 285
Number of extensions: 17
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 332
Length of database: 331
Length adjustment: 28
Effective length of query: 304
Effective length of database: 303
Effective search space:    92112
Effective search space used:    92112
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