GapMind for catabolism of small carbon sources

 

Alignments for a candidate for opuBA in Frankia alni ACN14a

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 WP_083867024.1 FRAAL_RS19080 ABC transporter ATP-binding protein

Query= TCDB::Q9RQ06
         (407 letters)



>NCBI__GCF_000058485.1:WP_083867024.1
          Length = 397

 Score =  160 bits (405), Expect = 6e-44
 Identities = 80/227 (35%), Positives = 133/227 (58%), Gaps = 6/227 (2%)

Query: 39  GATVGVYDTNFEINEGEIFVIMGLSGSGKSTLLRLLNRLIEPTSGKIFIDDQDVATLNKE 98
           G    V D + E+ +G+  V++G SG GK+TLLR++  L+EP+ G+I + ++D+  L   
Sbjct: 14  GDVRAVDDISLEVADGDFLVLLGPSGCGKTTLLRMIAGLLEPSEGRILLGERDITHL--- 70

Query: 99  DLLQVRRKSMSMVFQNFGLFPHRTILENTEYGLEVQNVPKEERRKRAEKALDNANLLDFK 158
                R++ ++MVFQ++ L+PH ++  N  + L    VP+ E R+R  +      L    
Sbjct: 71  ---PARQRDLAMVFQSYALYPHLSVERNIGFPLRAARVPRAEIRRRVREVAGQLELDHLL 127

Query: 159 DQYPKQLSGGMQQRVGLARALANDPEILLMDEAFSALDPLIRREMQDELLELQAKFQKTI 218
            + P++LSGG +QRV L RAL  DP+  LMDE  S LD  +R   + EL  L  +  +T 
Sbjct: 128 ARRPRELSGGQRQRVALGRALVRDPQAFLMDEPLSNLDAKLRTATRTELTALHRRLGRTF 187

Query: 219 IFVSHDLNEALRIGDRIAIMKDGKIMQIGTGEEILTNPANDYVKTFV 265
           ++V+HD  EA+ +  R+A++  G++ Q+GT  E+   PA+ +V  F+
Sbjct: 188 VYVTHDQVEAMSMATRVALLSGGRVEQVGTPTEVYDTPASVFVAGFL 234


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: 318
Number of extensions: 13
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: 397
Length adjustment: 31
Effective length of query: 376
Effective length of database: 366
Effective search space:   137616
Effective search space used:   137616
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 Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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