GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Cupriavidus basilensis 4G11

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 RR42_RS32890 RR42_RS32890 ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__Cup4G11:RR42_RS32890
          Length = 322

 Score =  194 bits (492), Expect = 3e-54
 Identities = 126/317 (39%), Positives = 179/317 (56%), Gaps = 18/317 (5%)

Query: 19  LLAFARKHRTILFLL-LLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVILIGG 77
           L A AR     LF L LL  +   A++ FLT  N LN+L + S+  ++A G+T VIL GG
Sbjct: 10  LSADARSFAYRLFALGLLCLLLAVASDAFLTLGNILNVLRQASLLFLLASGVTLVILTGG 69

Query: 78  IDVAVGSLLAFASIAAAYVVTAV------VGDGPATWLIALLVSTLIGLAGGYVQGKAVT 131
           +D++VG+ +A ++  AA V+ A       VG G  T         LIGLA G +    V 
Sbjct: 70  LDLSVGANVAMSACVAATVMKATGSTMLGVGAGLGT-------GALIGLANGLL----VA 118

Query: 132 WLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWWGSGEILFLPVPVVIFALVAA 191
            L +P FI T G + V  G T     G  I GF  A+R  GSG +  +P+PV +  +   
Sbjct: 119 MLRIPPFIATYGMLWVLHGVTYWFMAGETIHGFPPAFRAIGSGYLWGVPIPVYLMLVFLV 178

Query: 192 AGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGS 251
           AG    + T YG+++YA+G N  AARLSGV V      VY + GA+AG++  +  ARL S
Sbjct: 179 AGTAMSQKTTYGQEIYAIGANPVAARLSGVPVRRRLVLVYLVSGAMAGIASLVFLARLNS 238

Query: 252 AEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQV 311
           AE   G    L  IA+V+IGG SL GG G V GT++GA+++ ++ NG+ +L V++  Q +
Sbjct: 239 AEGDIGEALTLPAIAAVLIGGTSLFGGVGRVSGTLVGAIILTLVLNGMNLLTVSANWQPL 298

Query: 312 VIGLIIVAAVAFDHYAR 328
           V G+I+V AV  D  +R
Sbjct: 299 VTGVIVVLAVFLDTLSR 315


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: 260
Number of extensions: 19
Number of successful extensions: 2
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: 322
Length adjustment: 28
Effective length of query: 304
Effective length of database: 294
Effective search space:    89376
Effective search space used:    89376
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 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