GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Halomonas desiderata SP1

Align L-iditol 2-dehydrogenase (EC 1.1.1.14) (characterized)
to candidate WP_086509112.1 BZY95_RS06260 formaldehyde dehydrogenase, glutathione-independent

Query= BRENDA::P35497
         (357 letters)



>NCBI__GCF_002151265.1:WP_086509112.1
          Length = 397

 Score =  107 bits (267), Expect = 5e-28
 Identities = 100/312 (32%), Positives = 143/312 (45%), Gaps = 49/312 (15%)

Query: 1   MSQNSNPAVVLEKVGDIAIEQRPIPTI-----KDPHYVKLAIKATGICGSDIHYYRSGGI 55
           MSQ +N  VV +  G + +E  P P +     K  H V L +  T ICGSD H  R    
Sbjct: 1   MSQ-ANRGVVYKGPGKVDVESIPYPELALGNRKCDHGVILKVVTTNICGSDQHMVR---- 55

Query: 56  GKYILKAPMVLGHESSGQVVEVGDAVTRVKVGDRVAIEPGVPSRYSDETKEGRYNLC--- 112
           G+    A +VLGHE +G VVE G  V  +K GD V++   +        KEGR  +C   
Sbjct: 56  GRTTAPAGLVLGHEITGLVVECGRDVEFIKPGDLVSVPFNIACGRCRNCKEGRTGICLNV 115

Query: 113 -PHMAFAATPPID-----GTLVKYYLSP-EDF-LVKLPEGVSYEEGA-----CVEPLSVG 159
            P    AA   +D     G   +Y + P  DF L+K P+     E         +    G
Sbjct: 116 NPARPGAAYGYVDMGGWVGGQTEYVMVPYADFNLLKFPDSDQAMEKIRDLTLLSDIFPTG 175

Query: 160 VHSNKLAGVRFGTKVVVFGAGPVGLLTGAVARAFGATDVIFVDVFDNKLQRAKDFGATNT 219
            H    AGV  G+ V + GAGPVGL   A A+  GA  VI  D+ + +L +A+ FG   T
Sbjct: 176 FHGCVTAGVGPGSTVYIAGAGPVGLAAAASAQLLGAACVIVGDMIEERLAQARSFGC-ET 234

Query: 220 FNSSQFSTDKAQDLADGVQKLLGGNHADVVFECSG--ADVC------------IDAAVKT 265
            + +Q       D+AD ++ +LG    D   +C G  A  C            +++A++ 
Sbjct: 235 IDLTQ-----EGDMADKLEAILGEREVDCFVDCVGFEAHACGCNHDKEAPATVLNSAMQM 289

Query: 266 TKVGGTMVQVGM 277
           T+ GG   Q+G+
Sbjct: 290 TRAGG---QIGI 298


Lambda     K      H
   0.318    0.137    0.403 

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: 373
Number of extensions: 22
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: 357
Length of database: 397
Length adjustment: 30
Effective length of query: 327
Effective length of database: 367
Effective search space:   120009
Effective search space used:   120009
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 24 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