GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Sinorhizobium meliloti 1021

Align (S)-2-hydroxy-acid oxidase (EC 1.1.3.15); L-lactate oxidase (EC 1.1.3.2) (characterized)
to candidate SMc01740 SMc01740 L-lactate dehydrogenase (cytochrome) protein

Query= BRENDA::A9QH69
         (390 letters)



>FitnessBrowser__Smeli:SMc01740
          Length = 364

 Score =  154 bits (389), Expect = 4e-42
 Identities = 111/342 (32%), Positives = 155/342 (45%), Gaps = 16/342 (4%)

Query: 25  DFVNVFDLEKMAQKVIPKGAFGYIASGAGDTFTLHENIRSFNHKLIVPHGLKGVENPSTE 84
           DF ++ ++ + AQ  +PK  +  +  GA    TL  N  + +     P  L+ V      
Sbjct: 15  DFESLQEIIQKAQGALPKEKWDSLVGGAETETTLKRNRLAIDSIAFKPRVLRNVSVVDLS 74

Query: 85  ITFDGDKLASPIILAPVAAHKLANEQGEIASAKGVKEFGTIYTTSSYSTTDLPEISQTLG 144
           I   G +L  PI LAP     L    G  A A G + FG  +  SS   T L  +++   
Sbjct: 75  IEHFGRRLRLPIFLAPTGPLNLFGPGGGAAVASGAQVFGVAHMLSS-GCTPLESVAEAAP 133

Query: 145 DSPHWFQFYYSKDDGINRHIMDRLKAEGVKSIVLTVDATVGGNREVDKRNGFVFPVGMPI 204
            +    Q Y   DD      + R  A G  +I LTVD+ V   R+ D            I
Sbjct: 134 SALRMAQLYVRGDDASVHKYVGRALASGCAAICLTVDSAVLARRDRD------------I 181

Query: 205 VQEYLPNGAGKTMDYVYKATKQALSPKDVEYIAQYSGLPVYVKGPQCAEDAFRALEAGAS 264
              +   G GK     Y+A    L  + V+ I     +P+ +KG    EDA  A++ G  
Sbjct: 182 ANRHRTAGLGKWPGQAYQA---GLDWRTVKLIKDSYDIPLVLKGIATVEDARIAVDHGVD 238

Query: 265 GIWVTNHGGRQLDGGPAAFDSLQEVAEAVDRRVPIVFDSGVRRGQHVFKALASGADLVAL 324
            I+V+NHGGRQLD G    D L E+ +AV  +  ++ D G  RG  + KALA GA+LV L
Sbjct: 239 WIYVSNHGGRQLDHGRGTMDVLPEIIDAVGGQAKVMVDGGFCRGTDIIKALAIGANLVGL 298

Query: 325 GRPVIYGLAMGGSVGTRQVFEKINDELKMVMQLAGTQTIDDV 366
           GR   Y LA GG     ++ E I DE+   M L G  TI D+
Sbjct: 299 GRMQCYALAAGGEAAIIRMLELIEDEMLRSMALLGVPTIGDL 340


Lambda     K      H
   0.316    0.135    0.388 

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: 361
Number of extensions: 18
Number of successful extensions: 3
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: 390
Length of database: 364
Length adjustment: 30
Effective length of query: 360
Effective length of database: 334
Effective search space:   120240
Effective search space used:   120240
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 (21.6 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