GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Cereibacter sphaeroides ATCC 17029

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_011841961.1 RSPH17029_RS14660 ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>NCBI__GCF_000015985.1:WP_011841961.1
          Length = 330

 Score =  198 bits (504), Expect = 1e-55
 Identities = 118/315 (37%), Positives = 179/315 (56%), Gaps = 11/315 (3%)

Query: 14  KPRFDLLAFARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVI 73
           +PRF L         +L L +L+A+    N  FL+  N  N+L+  +  GIIAVGMTFVI
Sbjct: 8   RPRFHLHVLG----PLLALFVLIALGAWLNPNFLSYGNVTNVLARSAFIGIIAVGMTFVI 63

Query: 74  LIGGIDVAVGSLLAFAS---IAAAYVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAV 130
             GGID++VGS+ AF +   I +   +   +G+G +   + +LV+   GL  G++ G  +
Sbjct: 64  TSGGIDLSVGSMAAFIAGLMILSMNALLPHMGEGVSVIFVGVLVAAGAGLLAGWLNGFLI 123

Query: 131 TWLHVPAFIVTLGGMTVWRGATLLLNDGGPIS---GFNDAYRWWGSGEILFLPVPVVIFA 187
             + +  FIVTLG M ++R     L DGG +S   G    YR    G IL +  P+++FA
Sbjct: 124 AKVGIEPFIVTLGTMGIYRSLVTWLADGGTLSLDFGLRGLYRPVYYGGILGVAWPIIVFA 183

Query: 188 LVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSA 247
           +VA  G + +R T +GR V A+G N + AR S V V  +  + YA++G L G++  +   
Sbjct: 184 IVAILGEIVMRQTAFGRHVAAIGANEQVARYSAVKVPRVRIATYALLGLLVGIATIMYVP 243

Query: 248 RLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTS- 306
           RLGSA    G  +EL  IA+V+IGG  L GG G V GTV+G L++ ++ N L +  + S 
Sbjct: 244 RLGSASGSTGVLWELEAIAAVIIGGTVLKGGYGRVWGTVVGVLILSLIDNILNLASIVSP 303

Query: 307 YVQQVVIGLIIVAAV 321
           Y+   + G+I++ AV
Sbjct: 304 YLNGTIQGVIVILAV 318


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: 294
Number of extensions: 21
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: 330
Length adjustment: 28
Effective length of query: 304
Effective length of database: 302
Effective search space:    91808
Effective search space used:    91808
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 Apr 10 2024. 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