GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Pseudomonas simiae WCS417

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate GFF2753 PS417_14040 alkyl hydroperoxide reductase

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__WCS417:GFF2753
          Length = 521

 Score =  160 bits (405), Expect = 6e-44
 Identities = 109/316 (34%), Positives = 164/316 (51%), Gaps = 27/316 (8%)

Query: 9   VIILGSGPAGYSAAVYAARANLKPLLITGMQA---GGQLTTTTEVDNWPGDVHGLTGPAL 65
           V+++G GPAG SAA+YAAR  ++    TG+ A   GGQ+  T  ++N+   V    GP L
Sbjct: 214 VLVVGGGPAGSSAAIYAARKGIR----TGVAAERFGGQVLDTMSIENFIS-VQETEGPKL 268

Query: 66  MERMREHAERFETEIVFDHINAVDFAAKPYTLTGD--------SATYTCDALIIATGASA 117
              +  H  +++ +I+  ++     +  P    GD         AT     +I+ATGA  
Sbjct: 269 ASALEAHVRQYDVDIM--NLQRAS-SLVPAKNAGDLHEIRFESGATLKSKTVILATGARW 325

Query: 118 RYLGLPSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHR 177
           R +G+P E+ +  KGV  C  CDG  ++ K VAV+GGGN+ VE A+ LA I S VTL+  
Sbjct: 326 REMGVPGEQEYKAKGVCFCPHCDGPLFKGKRVAVIGGGNSGVEAAIDLAGIVSHVTLLEF 385

Query: 178 RETFRAEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNND-GSFDELKVD 236
               RA+ +L  KL    +   + +  +A   EV GD   VTG   K+ D G F  + ++
Sbjct: 386 DSKLRADAVLQRKL---YSLPNVDVITSALTSEVKGDGQKVTGLAYKDRDSGEFKTIDLE 442

Query: 237 GVFIAIGHTPNTSLFEGQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAIT 296
           G+F+ IG  PNT   +G + L     ++   R      TS+ G+FAAGDV    Y+Q + 
Sbjct: 443 GIFVQIGLLPNTDWLKGTVELTPRGEIIVDARG----ETSLPGVFAAGDVTTVPYKQIVI 498

Query: 297 SAGAGCMAALDTERYL 312
           + G G  A+L    +L
Sbjct: 499 AVGEGAKASLSAFDHL 514


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: 383
Number of extensions: 21
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: 521
Length adjustment: 31
Effective length of query: 289
Effective length of database: 490
Effective search space:   141610
Effective search space used:   141610
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 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