GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gadh2 in Azospirillum brasilense Sp245

Align gluconate 2-dehydrogenase (EC 1.1.1.215) (characterized)
to candidate AZOBR_RS04080 AZOBR_RS04080 cytochrome C

Query= BRENDA::Q5FRK5
         (437 letters)



>FitnessBrowser__azobra:AZOBR_RS04080
          Length = 288

 Score =  118 bits (296), Expect = 2e-31
 Identities = 95/305 (31%), Positives = 137/305 (44%), Gaps = 45/305 (14%)

Query: 6   VIACFLGMGLTAEATAQDSDKAIVEKGRYLA-AASDCAACHSVHGKP------EYSGGVS 58
           V AC +  G+ A A A+   ++ VE+GR L      C  CH+  G        E +GG  
Sbjct: 10  VAACLMLSGMIATAGAETPPESPVERGRALVNGIVACGNCHTPQGPNGPVAGRELAGGTP 69

Query: 59  FSLPMGKIYSTNITPDPDHGIGRYTEAQFGQALRQGIRRDGSTLYPAMPFPSYARLTDSD 118
           F       Y++NITPDP+ GIGR+T+ Q   A+R+G R DGS + P MPF  Y  L+D D
Sbjct: 70  FVEEPFTAYASNITPDPETGIGRWTDEQLIAAIREGRRPDGSLIGPPMPFGFYRGLSDGD 129

Query: 119 IHALFVYFRDGVKAVPVSAPRNEIPWPLSIRWPLTFWRWAFAPTPHKAITSTAGEF--TD 176
           + A+  Y R  V  V  S P++E    L              P  +     +  E   TD
Sbjct: 130 LRAIVAYLR-SVPPVRHSVPKSEYRMAL--------------PAAYGPPVGSVAEIPRTD 174

Query: 177 PLLARGAYLVEGPAHCGACHSPRAITMQEKALIAHDGSLYL----AGGAPVDG-W---TP 228
           P +  GAY+     HC  CH+P          +  DG L +    AGG    G W     
Sbjct: 175 P-VTYGAYMAGPLGHCMECHTP----------MLPDGRLDMTRMGAGGRNFTGPWGNAVS 223

Query: 229 PSLRQENRTGLGRWSEEDIVSFLRTGRSNPGSVFGSMTSAVLHGTQKLTDNDLHAIAHYL 288
            ++ Q+   GLG W++ +I   +  G    G           H  + ++D +L A+  YL
Sbjct: 224 RNITQDKEHGLGGWTDAEIRKAITEGVRPDGHRLSPPMG--YHYYKSMSDGELGALVAYL 281

Query: 289 KSLPP 293
           ++LPP
Sbjct: 282 RTLPP 286


Lambda     K      H
   0.319    0.133    0.420 

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: 497
Number of extensions: 39
Number of successful extensions: 10
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 437
Length of database: 288
Length adjustment: 29
Effective length of query: 408
Effective length of database: 259
Effective search space:   105672
Effective search space used:   105672
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. 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