GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Desulfovibrio vulgaris Miyazaki F

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate 8499635 DvMF_0401 Thioredoxin-disulfide reductase (RefSeq)

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Miya:8499635
          Length = 307

 Score =  171 bits (433), Expect = 2e-47
 Identities = 105/309 (33%), Positives = 165/309 (53%), Gaps = 13/309 (4%)

Query: 10  IILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPALMERM 69
           I++G GPAG +AA+Y  R+ +    +  +  GGQ+  T E++N+PG   G+ G  L +  
Sbjct: 7   IVIGGGPAGMTAALYLLRSGVSVAFVEKLSPGGQVLMTAEIENYPGFPKGIQGWELADLF 66

Query: 70  REHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYLGLPSEEAFM 129
             H ER+  +   D + A + A     +           +++ +GA  + LGLP E+  +
Sbjct: 67  AAHLERYPHDKYNDAVTAFEPAPGANRVRVGDEWIVGKTVVVCSGARYKKLGLPDEDRLI 126

Query: 130 GKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAEKILID 189
           GKG+S CA CDG F+R + V VVGGGN+A+EE+LYLA + + + LIHRR+ FR  K   +
Sbjct: 127 GKGISYCALCDGNFFRGQKVGVVGGGNSALEESLYLAKLVANLHLIHRRDEFRGCKCYQE 186

Query: 190 KLNARVAEGKIILKLNANLDEVLGDN--MGVTGARLKNNDGSFDELKVDGVFIAIGHTP- 246
           K+    +   I ++ ++ + ++ GD    G+T A +K  +  F  L +DG+FI IG  P 
Sbjct: 187 KVQ---SAPNIDIEFSSVVRKLHGDTGLTGITLADVKTGEERF--LPLDGLFIFIGFEPV 241

Query: 247 NTSLFEGQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAGCMAAL 306
              L +G      G+++           TS+ G+FAAGD+     RQ  T+ G G  AA 
Sbjct: 242 GDFLPDGIDKDPQGFIITD-----TEMRTSLPGVFAAGDIRSKACRQVTTAVGDGATAAT 296

Query: 307 DTERYLDGL 315
               YL+ L
Sbjct: 297 AAFTYLEQL 305


Lambda     K      H
   0.318    0.135    0.386 

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: 19
Number of successful extensions: 4
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: 320
Length of database: 307
Length adjustment: 27
Effective length of query: 293
Effective length of database: 280
Effective search space:    82040
Effective search space used:    82040
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: 48 (23.1 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