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_012050571.1 SWIT_RS22230 PQQ-dependent sugar dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_000016765.1:WP_012050571.1
          Length = 377

 Score =  164 bits (414), Expect = 5e-45
 Identities = 131/347 (37%), Positives = 174/347 (50%), Gaps = 48/347 (13%)

Query: 22  RVEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFR-EGRLSTYAE-LPVYHRGESGLLG 79
           +VEEV    + PWA+ FLP G ML+ E+ GR+ L   +G   T  E +P       G LG
Sbjct: 41  KVEEVAR-FDSPWAMTFLPGGHMLVTEKAGRLLLLSPDGARRTAVEGVPAVDSSGQGALG 99

Query: 80  -LALHPRFPEAPYVYAYRTVAEGGLRNQVVRLRHLGER-GVLDRVVLDGIPA--RPHGLH 135
            +  HP F     VY   + +  G  N +V  R  G+  G L    L+G+    R H L 
Sbjct: 100 EVVAHPDFATNGLVYF--SYSAPGSPNGIVLAR--GKLVGDLGGARLEGVTTLYRAHPLK 155

Query: 136 SGG----RIAFGPDGMLYVTTGEVYERELAQDLASLGGKILRLTPEGEPAPGNPFLGRRG 191
           SGG    RIAF PDG L+ + GE  +   AQ+   + GK++RLT +G+PAPGNP L  +G
Sbjct: 156 SGGHYAGRIAFSPDGHLFFSMGERQKFTPAQEPDGVLGKVVRLTMDGQPAPGNP-LAAKG 214

Query: 192 ARPEVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRVVGR 251
             P V+S GHRNP GLA+  + G L+ +E GP      G DEVNLI+PG NYGWP +V  
Sbjct: 215 FDPAVWSYGHRNPLGLAFDLE-GRLWDAEMGPK-----GGDEVNLILPGRNYGWP-IVSN 267

Query: 252 GND------------PRYRDPLYFWPQGFPPGNLAFFRGDLY--------VAGLRGQALL 291
           G+             P +  P   W     P +L  + G L+        V  L G+ L+
Sbjct: 268 GDHYDGKPIPDHVTRPEFEAPKVSWNPSISPSSLLVYSGKLFPQWRGKALVGALSGEMLI 327

Query: 292 RLVLEGERGRWRVLRVETALSGFGRLREVQVGPDGALYVTTSNRDGR 338
            LV  GE G     + E   +   R+R V  GPDGA+YV      GR
Sbjct: 328 -LVDLGEEG----AKEEARYAMGQRIRAVDQGPDGAVYVLEDKAGGR 369


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: 585
Number of extensions: 54
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: 352
Length of database: 377
Length adjustment: 29
Effective length of query: 323
Effective length of database: 348
Effective search space:   112404
Effective search space used:   112404
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: 49 (23.5 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