GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Halomonas desiderata SP1

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_086510147.1 BZY95_RS11910 PQQ-dependent sugar dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_002151265.1:WP_086510147.1
          Length = 416

 Score =  186 bits (473), Expect = 7e-52
 Identities = 129/364 (35%), Positives = 178/364 (48%), Gaps = 56/364 (15%)

Query: 21  LRVEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFREGRLSTYAELPVYHRGES----- 75
           L V +VVGG+E PWA+A+LPD  MLI  RPGR+ L     ++    LP     E      
Sbjct: 53  LTVTQVVGGIEHPWAVAWLPDERMLITARPGRLYLVDGDEVTEVGNLPKIDTDEDQLTAP 112

Query: 76  ------GLLGLALHPRFPEAPYVYAYRTVAEGGLRNQVVRLRHLGERGVLDRVVL--DG- 126
                 GLL + +HP +    ++Y   T +  G  + V+     G    L R  L  DG 
Sbjct: 113 EGGNQGGLLDVVVHPDYENNGWIYF--TYSSPGDDDSVMGDDEYGTGTALARARLSDDGS 170

Query: 127 -----------IPARPHGLHSGGRIAFGPDGMLYVTTGEVYERELAQDLASLGGKILRLT 175
                      +P    G H G RI F  DG +  + G+   R  +QDL   GG I+RL 
Sbjct: 171 ELTDLETIYAQVPRTAPGRHYGSRIVFPGDGSVMFSIGDRGIRYPSQDLTDPGGSIIRLH 230

Query: 176 PEGEPAPGNPFLGRR--GARPEVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDE 233
            +G    GNPF+       RPE++S GHRN QGLA HP+TGEL++ +HGPSG    G ++
Sbjct: 231 EDGGAFEGNPFIEAEPGNLRPEIFSYGHRNNQGLALHPETGELWAIDHGPSG----GGEQ 286

Query: 234 VNLIVPGGNYGWPRV-VGRGND-----------PRYRDPLYFWPQGFPPGNLAFFRGD-- 279
           + +   G N+GWP+V  GR  D           P  + P++ W     P  L F+ GD  
Sbjct: 287 LYVAEAGSNHGWPQVSFGREYDTDEFIGIGEVAPGVKPPVHVWEDTLAPSGLTFYTGDEF 346

Query: 280 ------LYVAGLRGQALLRLVLEGERGRWRVLRVETALSGFGRLREVQVGPDGALYVTTS 333
                 L++  L  + L R+VL+GE      + +E  L   GR+R+V+ GPDG LYV T 
Sbjct: 347 PGWQGNLFIGALYAERLHRVVLDGEAIAHEEILLENEL---GRIRDVRQGPDGLLYVLTD 403

Query: 334 NRDG 337
             DG
Sbjct: 404 ESDG 407


Lambda     K      H
   0.322    0.146    0.460 

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: 626
Number of extensions: 45
Number of successful extensions: 7
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: 352
Length of database: 416
Length adjustment: 30
Effective length of query: 322
Effective length of database: 386
Effective search space:   124292
Effective search space used:   124292
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 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