GapMind for catabolism of small carbon sources

 

Alignments for a candidate for opuBA in Klebsiella michiganensis M5al

Align BusAA, component of Uptake system for glycine-betaine (high affinity) and proline (low affinity) (OpuAA-OpuABC) or BusAA-ABC of Lactococcus lactis). BusAA, the ATPase subunit, has a C-terminal tandem cystathionine β-synthase (CBS) domain which is the cytoplasmic K+ sensor for osmotic stress (osmotic strength)while the BusABC subunit has the membrane and receptor domains fused to each other (Biemans-Oldehinkel et al., 2006; Mahmood et al., 2006; Gul et al. 2012). An N-terminal amphipathic α-helix of OpuA is necessary for high activity but is not critical for biogenesis or the ionic regulation of transport (characterized)
to candidate BWI76_RS06035 BWI76_RS06035 ferric transporter ATP-binding subunit

Query= TCDB::Q9RQ06
         (407 letters)



>FitnessBrowser__Koxy:BWI76_RS06035
          Length = 348

 Score =  184 bits (466), Expect = 5e-51
 Identities = 91/236 (38%), Positives = 155/236 (65%), Gaps = 6/236 (2%)

Query: 34  ILKKTGATVGVYDTNFEINEGEIFVIMGLSGSGKSTLLRLLNRLIEPTSGKIFIDDQDVA 93
           + K+ G+ + + + N  I +G++  ++G SG GK+T+LRL+  L +P+ G+I+ID +DV 
Sbjct: 12  VTKRFGSNMVIDNINLTIPQGQMVTLLGPSGCGKTTILRLVAGLEKPSEGQIYIDGEDVT 71

Query: 94  TLNKEDLLQVRRKSMSMVFQNFGLFPHRTILENTEYGLEVQNVPKEERRKRAEKALDNAN 153
             +      ++++ + MVFQ++ LFPH ++ +N  YGL++  VP+ + + R ++AL   +
Sbjct: 72  HRS------IQQRDICMVFQSYALFPHMSLGDNVGYGLKMLGVPRGDVKARVKEALAMVD 125

Query: 154 LLDFKDQYPKQLSGGMQQRVGLARALANDPEILLMDEAFSALDPLIRREMQDELLELQAK 213
           L  F+D+Y  Q+SGG QQRV LARAL   P++LL DE  S LD  +RR M+D++ ELQ +
Sbjct: 126 LEGFEDRYVDQISGGQQQRVALARALILKPKVLLFDEPLSNLDANLRRSMRDKIRELQKQ 185

Query: 214 FQKTIIFVSHDLNEALRIGDRIAIMKDGKIMQIGTGEEILTNPANDYVKTFVEDVD 269
           F  T ++V+HD +EA  + D + +M  G IMQIG+ +E+   PA+ ++ +F+ D +
Sbjct: 186 FDITSLYVTHDQSEAFAVSDTVLVMNKGHIMQIGSPQELYRQPASRFMASFMGDAN 241


Lambda     K      H
   0.316    0.135    0.364 

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: 271
Number of extensions: 14
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: 407
Length of database: 348
Length adjustment: 30
Effective length of query: 377
Effective length of database: 318
Effective search space:   119886
Effective search space used:   119886
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 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