GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-c in Pseudomonas fluorescens GW456-L13

Align alcohol dehydrogenase (cytochrome c) (EC 1.1.2.8) (characterized)
to candidate PfGW456L13_3925 Putative diheme cytochrome c-553

Query= BRENDA::D2SZY5
         (472 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3925
          Length = 412

 Score =  251 bits (641), Expect = 3e-71
 Identities = 156/420 (37%), Positives = 221/420 (52%), Gaps = 21/420 (5%)

Query: 12  AVAVGLLAGTSLAHAQNADEDLIKKGEYVARLGDCVACHTSLNGQKYAGGLSIKTPIGTI 71
           A+AVGL A    AHA +A    +K+GEY+AR  DC+ACHT+  G  YAGGL I +P GTI
Sbjct: 9   ALAVGLAAPVVAAHADDAQ---VKQGEYLARAADCMACHTAPGGAPYAGGLPIVSPFGTI 65

Query: 72  YSTNITPDPTYGIGTYTFKEFDEAVRHGVRKDGATLYPAMPYPSFARMTQDDMKALYAYF 131
           Y TNITP   +GIG Y   EF  A+  G R+DGA LYPAMPY S+  + + D  A++AY 
Sbjct: 66  YGTNITPSKEHGIGLYNDDEFFAALTEGKRRDGANLYPAMPYTSYHLIPRADSDAIHAY- 124

Query: 132 MHGVQPIAQKNHPTDISWPMSMRWPLSIWRSVFAPAPKDFTPAPGTDAEIARGEYLVTGP 191
           +  V+PI +    T +S+P ++R  L  W  ++    K   PA G      RG+Y+V   
Sbjct: 125 LKTVEPIERAAPVTSLSFPFNVRLGLMGWNMMYGKDVK-LEPAEGKSEAWKRGQYMVDVL 183

Query: 192 GHCGACHTPRGFGMQEKALDASGGPDFLGGGGVIDNWIAPSLRNDPVLGLGRWSDEDLFL 251
           GHCG CHTPRG       L  +   D    GG+++ ++APSL    +   G W+ +DL  
Sbjct: 184 GHCGECHTPRG-------LPGAMQMDKRMTGGILNGYLAPSLLATDLAARG-WNHQDLSS 235

Query: 252 FLKSGRTDHSAAFGGMADVVGWSTQYYTDADLHAMVKYIKSLPPVPPARGDYSYDASTAQ 311
           FLK G +     F  M  V   STQ  +D DL AM  ++  L   PPA            
Sbjct: 236 FLKHGMSAQGTMFNEMFPVFHNSTQGLSDPDLAAMATFL--LGDQPPAA-----KVLVEV 288

Query: 312 MLDSNNFSGNAGAKTYVEQCAICHRNDGGGVARMFPPLAGNPVVVSDNPTSVAHIVVDGG 371
            LD  + S   G + Y+  CA CH   G G   +   + GN  +  ++P ++  ++ DG 
Sbjct: 289 PLDKLSPSVQRGRQEYLNVCAGCHAPGGEGKPHIAVAMRGNTTLRLEDPRNLVRVIDDGI 348

Query: 372 VLPPTNWAPSAVAMPDYKNILSDQQIADVVNFIRSAWGNRAPANTTAADIQKLRLDHTPL 431
                +       MP + + L+D+Q+ D++N++R  WG + P +    D+QKLR D  PL
Sbjct: 349 GEQKFSGFEHMQPMPGFVDKLNDEQLTDLLNYLRQGWGGQ-PNDLAVNDVQKLRADAPPL 407


Lambda     K      H
   0.318    0.135    0.430 

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: 33
Number of successful extensions: 9
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: 472
Length of database: 412
Length adjustment: 32
Effective length of query: 440
Effective length of database: 380
Effective search space:   167200
Effective search space used:   167200
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 (21.7 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