GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Phaeacidiphilus oryzae TH49

Align Sugar ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_084704012.1 BS73_RS12870 ABC transporter ATP-binding protein

Query= uniprot:A0A165KQ08
         (355 letters)



>NCBI__GCF_000744815.1:WP_084704012.1
          Length = 406

 Score =  224 bits (572), Expect = 2e-63
 Identities = 136/327 (41%), Positives = 186/327 (56%), Gaps = 16/327 (4%)

Query: 15  GKGDKSVEVLRKVDIHVAPGEFLILVGPSGCGKSTLLNIIAGLDEPTEGEIRIGGKNVVG 74
           GK       L +VD  VAPG F++L+GPSG GK+TLL  +AG++ P  G IR+GG+ +  
Sbjct: 12  GKDYAGKTALHQVDFTVAPGRFMVLLGPSGSGKTTLLRCLAGIERPDRGSIRLGGRVLAQ 71

Query: 75  ----MPPRDRDIAMVFQSYALYPTLSVADNIGFALEMRKMPKPERQKRIDEVAAMLQ--- 127
               +PP  RD+AMVFQ YAL+P ++ A N+GFAL  R+   P+R     EVAA+L+   
Sbjct: 72  DRTHLPPDRRDLAMVFQDYALWPHMTAAANVGFALRRRR---PDRAAAAREVAAVLEQVG 128

Query: 128 ISHLLDRRPSQLSGGQRQRVAMGRALARQPQLFLFDEPLSNLDAKLRVEMRAEIKRLHQA 187
           + H  D  P QLSGG++QRVA+ RAL  +P L LFDEPLSNLDA LR  +R EI RL + 
Sbjct: 129 LGHRTDHYPHQLSGGEQQRVALARALVARPGLLLFDEPLSNLDADLRERLRVEIARLTRE 188

Query: 188 SGITSVYVTHDQVEAMTLGSRIAVMKGGVVQQLGTPDEIYNRPANTYVATFIG-SPTMNL 246
           SG T VY+THDQ EA  L   + V+  G + QLG+P+ IY RPA   VA F G S     
Sbjct: 189 SGATVVYITHDQAEAFALADEVGVLLDGRLAQLGSPEAIYRRPATASVARFTGVSAEFRG 248

Query: 247 LRGAVTGGQFGIQGAALNLAPPPSSANEVLLGVRPEHLVMQETAPWRGRVSVVEPTGPDT 306
             G   GG+ G      +  P  ++ +E +   R   ++++  A     +   +P+G D 
Sbjct: 249 RTGGAVGGEGGQVLVQTDAGPLRATVSEAVAADRAVRVMVRPDAV---GLRPADPSGND- 304

Query: 307 YVMVDTAAGSVTLRTDAQTRVQPGEHV 333
                 A G +    DA  R +  +HV
Sbjct: 305 -ARPGPAGGPLGRVVDAAFRGRGYDHV 330


Lambda     K      H
   0.318    0.135    0.388 

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: 437
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: 355
Length of database: 406
Length adjustment: 30
Effective length of query: 325
Effective length of database: 376
Effective search space:   122200
Effective search space used:   122200
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 (21.7 bits)
S2: 50 (23.9 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