GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Phaeobacter inhibens BS107

Align L-lactate oxidase (EC 1.1.3.2) (characterized)
to candidate GFF927 PGA1_c09430 l-lactate dehydrogenase IldD

Query= BRENDA::F8WQN2
         (384 letters)



>FitnessBrowser__Phaeo:GFF927
          Length = 401

 Score =  186 bits (473), Expect = 8e-52
 Identities = 119/386 (30%), Positives = 190/386 (49%), Gaps = 33/386 (8%)

Query: 9   LEEVEEEAKKVMPKMAFDYYSTGSDTCYTVGENRSCFSRYLLLPRMLRNVSRVDTSHELF 68
           L ++ + A++ +P+  ++Y  +G+ T  T   NR+   +    P +L      D S    
Sbjct: 13  LSDLRQRARRRLPRFVWEYLDSGTGTEATKARNRAALDQLGFAPSILHGPQTPDLSRRFL 72

Query: 69  GIRSSMPVWVAPMAMHGLAHPGREVATCRAAAAAGVPFTFSTVATSSLQEIQETGHDNRI 128
           GI   +P  VAP+ M GL  P  E    R AAA G+P+  STVA+ S +++ +       
Sbjct: 73  GIDRPLPFGVAPVGMSGLIWPDAERLLARCAAAQGLPYCLSTVASQSPEDLVDDLGAAPW 132

Query: 129 FQLYVIRNREVVRRWVTEAESRGFKALMVTVDAQRLGNREADARNKFTLPP--------- 179
           FQLY  ++ ++ R  +  A++ GF  L++TVD      RE   R+  T PP         
Sbjct: 133 FQLYPPKDPDIRRDLLARAKAAGFAGLVLTVDVPVASRRERQTRSGLTQPPRLTPRLLAQ 192

Query: 180 ---------GLALRNLEYLSSASTVQARDSQDGSGLMKLFTSEVD----DSLTWEFIPWL 226
                    G+A R L ++ +  T  +     G+G     T+ V      S  W+++ WL
Sbjct: 193 VAMRPAWAVGMARRGLPHMKTLDTYVS-----GAGASLSSTAHVGYLLRTSPDWDYVQWL 247

Query: 227 RGVTKLPIIVKGLLSPADAELAVQYGVDGIVVSNHGGRQLDYAPSGLHMLPAVVAAVRGC 286
           R     P+I+KG++   DA      G D + VSNH GRQ D APS +  LP + AA R  
Sbjct: 248 RDHWDGPLIIKGVMRAEDAAPLEAIGADALWVSNHAGRQFDAAPSTIEALPGIRAATR-- 305

Query: 287 GSSIPVLVDGGVRRGTDVIKALALGASGVLLGRPVLYGLAVGGQAGVERVLQLLRSEIEL 346
              +P++ D G+  G D+++ALALGA  V+LGR   + LA  G  G + ++ +LR +++ 
Sbjct: 306 ---LPLIFDSGIESGLDILRALALGADYVMLGRAFHFALAALGSRGPDHLVDILRKDLDA 362

Query: 347 SMALAGCSSVQQIGPQLLLPAPSAGP 372
           +M   G  ++  + P+ L  A  A P
Sbjct: 363 NMGQLGLETLSAL-PRPLGLASFANP 387


Lambda     K      H
   0.320    0.135    0.396 

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: 299
Number of extensions: 16
Number of successful extensions: 6
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: 384
Length of database: 401
Length adjustment: 31
Effective length of query: 353
Effective length of database: 370
Effective search space:   130610
Effective search space used:   130610
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: 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