GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Lutibaculum baratangense AMV1

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 WP_023430416.1 N177_RS01320 ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>NCBI__GCF_000496075.1:WP_023430416.1
          Length = 336

 Score =  199 bits (507), Expect = 6e-56
 Identities = 123/327 (37%), Positives = 179/327 (54%), Gaps = 13/327 (3%)

Query: 2   TAPSSPAPLATDKPRFDLLAFARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVSI 61
           +A   P+P A  +  F  L        +L L LL+ +    N  FL+  N  N+L+  + 
Sbjct: 6   SAARQPSPPARRRINFSALG------PLLALALLIVIGMLLNPNFLSYGNLTNVLARSAF 59

Query: 62  YGIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIALL---VSTLI 118
            GIIAVGMTFVI  GG+D++VGS+ AF +     V+  +V    A+WL+ L       L+
Sbjct: 60  IGIIAVGMTFVITSGGLDLSVGSMAAFIAGTMIIVMNLLVPSLGASWLVVLCGLGTGLLL 119

Query: 119 GLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPIS---GFNDAYRWWGSGE 175
           G   G V G  VT   + AFIVTLG M ++R     L DGG +S      + YR +  G 
Sbjct: 120 GALAGAVNGLLVTVGRIEAFIVTLGTMGIFRSLVTWLADGGTLSLDFTVREIYRPFYYGG 179

Query: 176 ILFLPVPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIG 235
           I  +  P+++FA+VA  G + +R T +GR   A+G N + AR S V VD +  S Y ++G
Sbjct: 180 IFGVAWPIIVFAIVAIIGEIVMRKTPFGRHCAAIGSNEQVARYSAVRVDLVRLSTYVLLG 239

Query: 236 ALAGLSGFLLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVL 295
            L G++  +   RLGSA +  G  +EL  IA+V+IGG  L GG G V GTV+G L++  +
Sbjct: 240 VLVGIATIMYVPRLGSASSSTGVLWELEAIAAVIIGGTVLKGGFGRVWGTVVGVLILSFI 299

Query: 296 SNGLVMLHVTS-YVQQVVIGLIIVAAV 321
            N L +  + S Y+   + G+II+ AV
Sbjct: 300 GNLLNLAALVSPYLNGAIQGVIIILAV 326


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: 17
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: 332
Length of database: 336
Length adjustment: 28
Effective length of query: 304
Effective length of database: 308
Effective search space:    93632
Effective search space used:    93632
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 24 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