GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Pedobacter sp. GW460-11-11-14-LB5

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate CA265_RS06300 CA265_RS06300 glucose dehydrogenase

Query= BRENDA::Q8ZUN8
         (371 letters)



>FitnessBrowser__Pedo557:CA265_RS06300
          Length = 362

 Score =  202 bits (514), Expect = 1e-56
 Identities = 126/349 (36%), Positives = 190/349 (54%), Gaps = 32/349 (9%)

Query: 30  PSEEWKFKISEVASDLEVPWSIAPLGGGRYLVTERPGRLVLISPSGKKLVASFDVANV-- 87
           P  + K K+  + S L +PW +          TE+ G++  ++P+  ++     +  V  
Sbjct: 31  PDVDLKSKV--IVSGLSLPWEMVYGPDNFIWFTEKAGKISRLNPANGQVTPLLTITEVRT 88

Query: 88  -GEAGLLGLALHPEFPKKSWVYLYASYFAEGGHIRNRVIRGRLDGSTFKLKEVKTLIDGI 146
            GE GLLG+ LHP+F    +VY+   Y   G   + +V+R    G      +V  L+D I
Sbjct: 89  NGEGGLLGMTLHPDFAGNPYVYVVYGY---GSTYKAKVVRYTYSGGGLTSPQV--LLDQI 143

Query: 147 PGAYIHNGGRIRFGPDGMLYITTGDAADPRLAQDLSSLAGKILRVDEEGRPPADNPFPNS 206
           P A IHNG R+     G L+I+TGDAAD    Q+++SLAGKILR++ +G  PADNP+PN+
Sbjct: 144 PAASIHNGSRLLIS-GGKLFISTGDAADTGNPQNVNSLAGKILRINLDGTIPADNPYPNN 202

Query: 207 PIWSYGHRNPQGIDWHRASGVMVATEHGPVGHDEVNIILKGGNYGWPLATG---KAGRGE 263
           P+WS GHRN QG+   +    + ++EHGP   DE+NII KG NYGWP   G   ++G   
Sbjct: 203 PLWSLGHRNAQGL--IQVGNKIFSSEHGPDSDDEINIIEKGRNYGWPNIKGYCNESGEQS 260

Query: 264 F------VDPVIDTGSETWAPSGASFVHGDMFPGLRGWLLIACLRGSMLAAVNFGD-NME 316
           F       +P+I+  + T APSG ++ + D  P  +  LL+A L+G+ L  +   D   +
Sbjct: 261 FCSSNNVAEPLIN-WTPTIAPSGLAYYNSDYIPQFKNSLLLAVLKGTKLMQLKLDDAQTK 319

Query: 317 VRKISTFFKNVFGRLRDVVIDDDGGILISTSNRDGRGSLRAGDDKILKI 365
           +     F+ N +GR+R +    +G I I TSN          DDKI++I
Sbjct: 320 ITGTKDFYVNTYGRIRAICQSPEGKIYICTSN--------GSDDKIVEI 360


Lambda     K      H
   0.320    0.140    0.432 

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: 377
Number of extensions: 18
Number of successful extensions: 7
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: 371
Length of database: 362
Length adjustment: 30
Effective length of query: 341
Effective length of database: 332
Effective search space:   113212
Effective search space used:   113212
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 (21.7 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