GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dgoD in Phaeobacter inhibens BS107

Align gluconate/galactonate dehydratase (EC 4.2.1.140); gluconate dehydratase (EC 4.2.1.39) (characterized)
to candidate GFF443 PGA1_c04540 putative d-galactonate dehydratase

Query= BRENDA::Q6L1T2
         (391 letters)



>FitnessBrowser__Phaeo:GFF443
          Length = 410

 Score =  185 bits (470), Expect = 2e-51
 Identities = 130/365 (35%), Positives = 181/365 (49%), Gaps = 19/365 (5%)

Query: 14  SPGEKSSPWSSTILIVKLTSSNGNIGYGEAPTTFMTLP-VKESMREV-ERVFKDQNYFNI 71
           +PG     W    ++VK+T+  G  G+GE     +    +   +R+V ER  +  N  NI
Sbjct: 15  APGWGGRYW----ILVKVTTDTGITGWGECYAASVGPDAMTHVIRDVFERHMQGMNPENI 70

Query: 72  EKNMREFYKHSFYLSRSMEATSALSAFEIASWDLIGKDLGTPVYNLLGGEYNSELRAYAN 131
           E   R  Y   F     +    A S  EIA WD++GKD   PV+ L+GG  N  LRAY  
Sbjct: 71  EWMFRRAYSSGFTQRPDLSVMGAFSGLEIACWDILGKDRDRPVHALIGGRMNDRLRAYTY 130

Query: 132 GWYSDCLEPDDF-------VSRAKEYIKKGYTAFKFDPFRNNFDRIGN----DGIKKAVD 180
            +     + D F          A   ++KGYTA KFDP      R G+      I ++V 
Sbjct: 131 LYPLPHHDIDAFWNTPELAAESAIAAVEKGYTAVKFDPAGPYTMRGGHMPAQSDITQSVA 190

Query: 181 IVSAMRSELGENIDLLIECHGRFSTKYAIKVGQALDEFNPLFIEEPIHPEMELGLFDFKR 240
              A+R  +G+  DLL   HG+F+   AI++GQAL+ + PL+ EEP  P++   +     
Sbjct: 191 FCRAIREAVGDRADLLFGTHGQFTPAGAIRLGQALESYEPLWFEEPTPPDLVADMARVAD 250

Query: 241 YVNTPVALGERLLNKEDFARYISQGMVDIVQADLTNSKGILEAKKISAIVESFGGLMAFH 300
            V  PVA GERL  K +FA  +  G  +I+Q  L  S GI E KKI+AI E FG  MA H
Sbjct: 251 RVRIPVATGERLTTKAEFAAILRAGAAEILQPALGRSGGIWETKKIAAIAEVFGAQMAPH 310

Query: 301 NAFGPVQTAATLNVDYTLTNFLIQESFEDSWPDWKRNLFSGYRIENGHFKLSGKPGLGIT 360
              GPV+ AA + +  ++ N L+ E+ E   P     +  G  +E+G    S  PGLGI 
Sbjct: 311 LYAGPVEWAANIQLAASIPNLLMIETIET--PFHTALIKQGITVEDGFVIPSDTPGLGIE 368

Query: 361 ADEKL 365
            DE L
Sbjct: 369 VDEDL 373


Lambda     K      H
   0.317    0.136    0.401 

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: 353
Number of extensions: 16
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: 391
Length of database: 410
Length adjustment: 31
Effective length of query: 360
Effective length of database: 379
Effective search space:   136440
Effective search space used:   136440
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: 50 (23.9 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