GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Rhizorhabdus wittichii RW1

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_011952282.1 SWIT_RS07285 PQQ-dependent sugar dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_000016765.1:WP_011952282.1
          Length = 530

 Score =  184 bits (466), Expect = 6e-51
 Identities = 136/373 (36%), Positives = 177/373 (47%), Gaps = 74/373 (19%)

Query: 22  RVEEVVGG--LEVPWALAFLPDGGMLIAERPGRIRLFREGRL--STYAELP--VYHRGES 75
           R E VVG   L+ PW++ FL    ML++ERPGR+R+   G       A +P  V+  G+ 
Sbjct: 152 RFETVVGEGRLDTPWSILFLSPDRMLVSERPGRLRIVTTGGEVGPPIANVPAIVHDFGQG 211

Query: 76  GLLGLALHPRFPEAPYVYAYRTVAE----GGLRN--------------QVVRLRHLGERG 117
           G+LGLA HP +    Y+Y   T       G  R               +V+R R  G   
Sbjct: 212 GILGLARHPDYRRNGYLYLAYTDEMPDRFGEARKCAGRIYCFSTASQLKVIRFRLAGN-A 270

Query: 118 VLDRVVLDGIPARPHGLHS--GGRIAFGPDGMLYVTTGE-VYERELAQDLASLGGKILRL 174
           ++DR  +       + L    GGR+AFG DGMLY+T G+  Y    AQD+A+  GKI R+
Sbjct: 271 MVDRTTIWQAAPESYRLSPSFGGRLAFGSDGMLYITVGDRAYSAMEAQDIATPNGKIHRV 330

Query: 175 TPEGEPAPGNPFLGRRGARPEVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEV 234
             +G   P NPF+G  GA P ++S GHRNPQGLA  P++G L+SSEHGP G      DE+
Sbjct: 331 ADDGHVPPDNPFVGVPGADPTIWSFGHRNPQGLAVDPRSGRLWSSEHGPRGG-----DEL 385

Query: 235 NLIVPGGNYGWPRVV-GRGNDPRYRDPLY----------------------------FWP 265
           NLI  GGNYGWP    G G D R  DP Y                             W 
Sbjct: 386 NLIRRGGNYGWPLATFGMGYDGRPFDPAYPLGHSQAAIELTAPSRPIDRAGFIAPVVHWT 445

Query: 266 QGFPPGNLAFFRG--------DLYVAGLRGQALLRLVLEGERGRWRVLRVETALSGFGRL 317
                 ++ F+ G         L V  LR Q LLRL +E +     V   E      G +
Sbjct: 446 PSIAVSSILFYSGTAFPAWRDSLLVTSLRQQKLLRLTIEHDA----VTEQELLFERHGNV 501

Query: 318 REVQVGPDGALYV 330
           R+V   PDG+LYV
Sbjct: 502 RDVAEAPDGSLYV 514


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: 669
Number of extensions: 51
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 1
Length of query: 352
Length of database: 530
Length adjustment: 32
Effective length of query: 320
Effective length of database: 498
Effective search space:   159360
Effective search space used:   159360
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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