GapMind for catabolism of small carbon sources

 

Alignments for a candidate for opuBA in Sphingomonas koreensis DSMZ 15582

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 Ga0059261_1870 Ga0059261_1870 ABC-type transport system involved in resistance to organic solvents, ATPase component

Query= TCDB::Q9RQ06
         (407 letters)



>FitnessBrowser__Korea:Ga0059261_1870
          Length = 273

 Score =  125 bits (313), Expect = 2e-33
 Identities = 73/210 (34%), Positives = 122/210 (58%), Gaps = 6/210 (2%)

Query: 48  NFEINEGEIFVIMGLSGSGKSTLLRLLNRLIEPTSGKIFIDDQDVATLNKEDLLQVRRKS 107
           + ++ +GEI  ++G SG+GKS L+R +  L EP +G I +  +DV  LN E+ +++R++ 
Sbjct: 35  DLDVRQGEILGVVGGSGTGKSVLMRSIIGLQEPDAGSIEVFGEDVQHLNTEEAIELRKR- 93

Query: 108 MSMVFQNFGLFPHRTILENTEYGLEVQNVPKEERRKRAEKALDNANLL----DFKDQYPK 163
             ++FQ   LF   T+ EN +  L+ +  P  ++    E A     +     D   +YP 
Sbjct: 94  WGVLFQGGALFSTLTVAENVQVPLK-EFYPAFDQALLDEIAAYKVVMTGLPSDAGPKYPA 152

Query: 164 QLSGGMQQRVGLARALANDPEILLMDEAFSALDPLIRREMQDELLELQAKFQKTIIFVSH 223
           +LSGGM++R GLAR+LA DPE+L +DE  + LDP+      +  L LQ     T+  ++H
Sbjct: 153 ELSGGMKKRAGLARSLALDPELLFLDEPTAGLDPIGAAAFDELTLALQRTLGLTVFLITH 212

Query: 224 DLNEALRIGDRIAIMKDGKIMQIGTGEEIL 253
           DL+    I DR+A++ D  ++ +GT +E+L
Sbjct: 213 DLDTLYAICDRVAVLADKHVIAVGTIDELL 242


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: 238
Number of extensions: 17
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: 407
Length of database: 273
Length adjustment: 28
Effective length of query: 379
Effective length of database: 245
Effective search space:    92855
Effective search space used:    92855
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: 49 (23.5 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