GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Acidovorax sp. GW101-3H11

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 Ac3H11_1841 Ribose ABC transport system, ATP-binding protein RbsA (TC 3.A.1.2.1)

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1841
          Length = 892

 Score =  180 bits (457), Expect = 1e-49
 Identities = 123/329 (37%), Positives = 184/329 (55%), Gaps = 13/329 (3%)

Query: 1   MTAPSSPA-PLATDKPRFDLLAFARKHRTILFLLL-LVAVFGAANERFLTARNALNILSE 58
           M AP++PA P AT        +    +  +L +L  +VA+F + +E F +A   + I +E
Sbjct: 563 MNAPTAPAAPAATPSSASVWRSQLGTYLGLLAVLAGMVALFSSLSEYFWSAETFITIANE 622

Query: 59  VSIYGIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIALLVSTLI 118
           +    ++AVGMTFV++I GID++VGS++A A+  +A  +       PA   +AL    + 
Sbjct: 623 IPALAVMAVGMTFVLIIAGIDLSVGSVMALAAATSAAAILQWGWTVPAAAALALATGLVC 682

Query: 119 GLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWWGS---GE 175
           G   G +   +V W  +P+FIV+LG +   RG+  ++ D        DA  W  +   G 
Sbjct: 683 GTITGAI---SVAW-RLPSFIVSLGMLEAVRGSAYVVTDSRT-QYVGDAISWLSAPFFGG 737

Query: 176 ILFLPVPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIG 235
           I F  +  V+  +VA    + L  T +GR V  +G N EA RL+GV+   I   V+A+ G
Sbjct: 738 ISFAFLLAVVLVVVA---QLVLSRTVFGRCVVGIGTNEEAMRLAGVDPRPIRVIVFAMTG 794

Query: 236 ALAGLSGFLLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVL 295
            LAGL+G + SARL +A+  AGTG EL+VIA+VVIGG SL GG G V  T  G L+I VL
Sbjct: 795 LLAGLAGLMQSARLEAADPNAGTGMELQVIAAVVIGGTSLMGGRGSVVNTAFGVLIIAVL 854

Query: 296 SNGLVMLHVTSYVQQVVIGLIIVAAVAFD 324
             GL  +  +   ++++ G +IVAAV  D
Sbjct: 855 EAGLAQVGASEPSKRIITGFVIVAAVIVD 883


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: 579
Number of extensions: 32
Number of successful extensions: 4
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: 892
Length adjustment: 35
Effective length of query: 297
Effective length of database: 857
Effective search space:   254529
Effective search space used:   254529
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: 52 (24.6 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