GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fdh in Halomonas desiderata SP1

Align D-threo-aldose 1-dehydrogenase (EC 1.1.1.122) (characterized)
to candidate WP_086510112.1 BZY95_RS11780 alcohol dehydrogenase AdhP

Query= BRENDA::Q97YM2
         (349 letters)



>NCBI__GCF_002151265.1:WP_086510112.1
          Length = 342

 Score =  136 bits (343), Expect = 7e-37
 Identities = 102/343 (29%), Positives = 167/343 (48%), Gaps = 15/343 (4%)

Query: 10  KAALLKKFSEPLSIEDVNIPEPQGEEVLIRIGGAGVCRTDLRVWKGVEAKQGFRLPIILG 69
           +AA+++KF EPL+IE+V +P P   EVL++I  +GVC TDL    G +       P I G
Sbjct: 6   RAAVVRKFGEPLAIEEVEVPRPGPGEVLVKIAASGVCHTDLHAAHG-DWPVKPNPPFIPG 64

Query: 70  HENAGTIVEVGELAK-VKKGDNVVV---YATWGDLTCRYCREGKFNICKNQIIPGQTTNG 125
           HE  G +  VG   K +K+GD + V   ++  G   C +C  G   +C++Q   G + NG
Sbjct: 65  HEGVGHVAAVGAGVKHLKEGDRIGVPWLHSACGH--CEHCLGGWETLCESQQNTGYSVNG 122

Query: 126 GFSEYMLVKSSRWLVKLNSLSPVEAAPLADAGTTSMGAIRQALPFISKFAEPVVIVNGIG 185
           GF++Y L  +       +++  VE AP+  AG T    + + L          V+++GIG
Sbjct: 123 GFADYTLAVADYAGHLPDNVGFVEVAPVLCAGVT----VYKGLKVTDTRPGQWVVISGIG 178

Query: 186 GLAVYTIQILKALMKNITIVGISRSKKHRDFALELGADYVSEMKDAESLINKLTDGLGAS 245
           GL    +Q  KA+  N+  V I  +K     A  LGA         +  +  L   +G +
Sbjct: 179 GLGHMAVQYAKAMGLNVAAVDIDDAK--LALAERLGASVTVNAAKTDP-VAYLKKAIGGA 235

Query: 246 IAIDLVGTEETTYNLGK-LLAQEGAIILVGMEGKRVSLEAFDTAVWNKKLLGSNYGSLND 304
             + +       +   + ++ + G I L G+      L  F+T +    + GS  G+  D
Sbjct: 236 HGVLVTAVSPKAFEQAQGMVRRGGTISLNGLPPGDFPLPIFETVLNGITVRGSIVGTRQD 295

Query: 305 LEDVVRLSESGKIKPYIIKVPLDDINKAFTNLDEGRVDGRQVI 347
           L++ +  +  GK+K  +    L++IN  F  L EGR++GR V+
Sbjct: 296 LQESLDFAGEGKVKATVSTDRLENINDVFQRLHEGRIEGRVVL 338


Lambda     K      H
   0.317    0.136    0.389 

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: 304
Number of extensions: 17
Number of successful extensions: 5
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: 349
Length of database: 342
Length adjustment: 29
Effective length of query: 320
Effective length of database: 313
Effective search space:   100160
Effective search space used:   100160
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: 49 (23.5 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