GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Marinobacter adhaerens HP15

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate GFF2249 HP15_2199 glucose/sorbosone dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>FitnessBrowser__Marino:GFF2249
          Length = 511

 Score =  197 bits (501), Expect = 5e-55
 Identities = 128/344 (37%), Positives = 176/344 (51%), Gaps = 39/344 (11%)

Query: 23  VEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFRE----GRLSTYAELPVYHRGESGLL 78
           VE +  GLE PW+LAFLP GG L+ ER GR+R+  E    G+       PV++  ++GL 
Sbjct: 173 VETLTSGLEHPWSLAFLPGGGALVTERAGRLRMISEEWELGQAPITGVPPVFNDAQAGLF 232

Query: 79  GLALHPRFPEAPYVYAYRTVAEGGLRNQVVRLRHLGERGVLDRV-VLDGIPARPHGLHSG 137
            + L P F     V+   +       +  V    L    + + V +    PA+    H G
Sbjct: 233 DVLLSPDFENNQLVFLAYSCGTASANHLCVARGQLQAEALTEVVEIFRAKPAKEGSAHYG 292

Query: 138 GRIAFGPDGMLYVTTGEVYE-RELAQDLASLGGKILRLTPEGEPAPGNPFLGRRGARPEV 196
           GR+A+ PDG L VT G+ ++ RE AQ+L+S  GKI+RL P+G     NPF+GR GA PE+
Sbjct: 293 GRMAWLPDGTLIVTLGDGFDYREQAQNLSSHLGKIVRLNPDGSVPADNPFVGREGALPEI 352

Query: 197 YSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRVVGRGND-- 254
           YS GHRN QGL +      L + EHGP      G DE+N+I PG NYGWP V+  G D  
Sbjct: 353 YSYGHRNVQGLVFDSVENVLIAHEHGPR-----GGDEINIIEPGHNYGWP-VITHGIDYT 406

Query: 255 ----------PRYRDPLYFWPQGFPPGNLAFFRGDLY--------VAGLRGQALLRLVLE 296
                          PL  W     P  +  +RG+L+        V  L  +++ R+ LE
Sbjct: 407 GAMITPFVEREGMEQPLLHWTPSIAPSGMTRYRGELFPDWQGNLLVGALADKSVHRVTLE 466

Query: 297 -GERGRWRVLRVETALSGFG-RLREVQVGPDGALYVTTSNRDGR 338
            GE        VE+     G R+R+V  GPDGA+Y+ T + DGR
Sbjct: 467 AGEAS-----DVESLFEAMGERIRDVATGPDGAVYLLTDSADGR 505


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: 576
Number of extensions: 39
Number of successful extensions: 8
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: 511
Length adjustment: 32
Effective length of query: 320
Effective length of database: 479
Effective search space:   153280
Effective search space used:   153280
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 Sep 17 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