GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Polaromonas naphthalenivorans CJ2

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_011801983.1 PNAP_RS13005 ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>NCBI__GCF_000015505.1:WP_011801983.1
          Length = 317

 Score =  169 bits (427), Expect = 1e-46
 Identities = 102/300 (34%), Positives = 160/300 (53%), Gaps = 7/300 (2%)

Query: 32  LLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVILIGGIDVAVGSLLAFASI 91
           LLL    F   NERFLT +N   I+ +V + G+IA+G T +IL  GID++ G ++A   I
Sbjct: 18  LLLACVFFATQNERFLTLQNFSLIMQQVMVVGVIAIGQTLIILTAGIDLSCGMVMALGGI 77

Query: 92  AAAYVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGA 151
               V+T +  D      +A+     + +  G + G  VT + +P FIVTLG + +    
Sbjct: 78  ----VMTKLSADFGLPTPVAIACGMAVTMLFGLINGLLVTRIKLPPFIVTLGTLNIAFAI 133

Query: 152 TLLLNDGGPISGFNDAYRWWGSGEIL---FLPVPVVIFALVAAAGHVALRYTRYGRQVYA 208
           T L +    ++       + G+   +    +   VV+   +  A  + LR T  GR +YA
Sbjct: 134 TQLYSQSQTVTDIPAGMTFLGNTFTIGNTSMGYGVVLMLALYVATWLWLRETAPGRHIYA 193

Query: 209 VGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGSAEAVAGTGYELRVIASV 268
           VG + EA RL+G+  D +   VY + G   G++  L  AR G+ +  AG    L  I +V
Sbjct: 194 VGNSPEATRLTGIATDRVLLGVYVLAGLFYGIASLLSVARTGAGDPNAGQTENLDAITAV 253

Query: 269 VIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQVVIGLIIVAAVAFDHYAR 328
           V+GG SL GG G + GT++GAL++GV  NGL ++ V+S  Q +V G++++ AV  D  +R
Sbjct: 254 VLGGTSLFGGRGMLLGTLVGALIVGVFRNGLTLMGVSSVYQVLVTGILVILAVTTDQMSR 313


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: 240
Number of extensions: 16
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: 317
Length adjustment: 28
Effective length of query: 304
Effective length of database: 289
Effective search space:    87856
Effective search space used:    87856
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: 48 (23.1 bits)

This GapMind analysis is from Apr 09 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