GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate WP_068171234.1 HTA01S_RS11580 ABC transporter permease

Query= uniprot:B2T9V8
         (351 letters)



>NCBI__GCF_001592305.1:WP_068171234.1
          Length = 345

 Score =  176 bits (447), Expect = 6e-49
 Identities = 116/319 (36%), Positives = 175/319 (54%), Gaps = 10/319 (3%)

Query: 28  GKRARSELARLRELALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAESLI 87
           GK    +L  +RE+ LL  +A+L V  +F SP FLT  N+ ++L + +   +VV+  +++
Sbjct: 27  GKPGGHKLTSMREMGLLAIIAVLCVGMSFASPYFLTWDNIRAMLLSFSIEGIVVVGMTIL 86

Query: 88  VLTGKFDLSLESTVGIAPAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFINGFL 147
           ++ G  DLS+ S V  A  V   L +           P  AGL+AI    A+IG + G  
Sbjct: 87  LIVGGIDLSVGSVVCFAMVVTGKLFLMGLD-------PWTAGLIAIAA-SAMIGAMIGGC 138

Query: 148 VVRLRLNAFIVTLAMLIVLRGMLVGATKGG--TLFDMPTSFFALATTIVLGLPLSVWLAA 205
           VVR+ LN FI +LA ++++RG+ +  T+G   +LF +P SF  +    V G+P  + +  
Sbjct: 139 VVRIGLNHFIASLAFMVIVRGLSLALTQGTPQSLFSLPESFKFIGQGTVFGMPAVIIIFL 198

Query: 206 AAFAIAAFMLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTG 265
               ++ F+LR   L R ++  G N +AA  +GIRV R+ + V VL +  A + G+I T 
Sbjct: 199 VIVVVSDFVLRRASLMRRVFYTGSNEKAALYSGIRVGRVKFWVTVLCAASAGLAGVIYTA 258

Query: 266 YVGAINANQGNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSF 325
             GA     G GM   V AAAVIGG SL GG GT+ GA+ G+ LL VV + L L  V  +
Sbjct: 259 RFGAATPTFGIGMELNVIAAAVIGGASLKGGSGTVLGAVLGLALLSVVTSSLILLDVSPY 318

Query: 326 WIQAIYGAIILGSLMVARL 344
           W   I G I+L ++ +  L
Sbjct: 319 WQDVIKGLILLAAVTIDHL 337


Lambda     K      H
   0.326    0.140    0.397 

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: 275
Number of extensions: 16
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: 351
Length of database: 345
Length adjustment: 29
Effective length of query: 322
Effective length of database: 316
Effective search space:   101752
Effective search space used:   101752
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 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