GapMind for catabolism of small carbon sources

 

Alignments for a candidate for drdehyd-cytc in Pseudomonas fluorescens GW456-L13

Align cytochrome c component of deoxyribose dehydrogenase (characterized)
to candidate PfGW456L13_3925 Putative diheme cytochrome c-553

Query= reanno::WCS417:GFF2133
         (447 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3925
          Length = 412

 Score =  228 bits (580), Expect = 4e-64
 Identities = 133/401 (33%), Positives = 201/401 (50%), Gaps = 28/401 (6%)

Query: 46  EPALVSRGEYVARLSDCVACHSLAGKAPFAGGLEMATPLGAIHATNITPDKSTGIGTYSL 105
           + A V +GEY+AR +DC+ACH+  G AP+AGGL + +P G I+ TNITP K  GIG Y+ 
Sbjct: 24  DDAQVKQGEYLARAADCMACHTAPGGAPYAGGLPIVSPFGTIYGTNITPSKEHGIGLYND 83

Query: 106 ADFDRAVRHGVAPGGRRLYPAMPYPSYVKLSDDDIKALYAFFMQGIKPANQPNIPSDIPW 165
            +F  A+  G    G  LYPAMPY SY  +   D  A++A +++ ++P  +    + + +
Sbjct: 84  DEFFAALTEGKRRDGANLYPAMPYTSYHLIPRADSDAIHA-YLKTVEPIERAAPVTSLSF 142

Query: 166 PLNMRWPIALWNGVFAPTATYAAKPDQDALWNRGAYIVQGPGHCGSCHTPRGLAFNEKAL 225
           P N+R  +  WN ++           +   W RG Y+V   GHCG CHTPRGL      +
Sbjct: 143 PFNVRLGLMGWNMMYGKDVKLEPAEGKSEAWKRGQYMVDVLGHCGECHTPRGLP-GAMQM 201

Query: 226 DEAGAPFLAGALLDGWYAPSLRQDPNTGLGRWSEPQIVQFLKTGRNAHAVVYGSMTEAFN 285
           D+     + G +L+G+ APSL        G W+   +  FLK G +A   ++  M   F+
Sbjct: 202 DKR----MTGGILNGYLAPSLLATDLAARG-WNHQDLSSFLKHGMSAQGTMFNEMFPVFH 256

Query: 286 NSTQFMQDDDLAAIARYLKSLPGDPQRDGAPWQYQAVAAVQDAP----------GAHTYA 335
           NSTQ + D DLAA+A +L    GD        Q  A   + + P          G   Y 
Sbjct: 257 NSTQGLSDPDLAAMATFLL---GD--------QPPAAKVLVEVPLDKLSPSVQRGRQEYL 305

Query: 336 TRCASCHGLDGKGQPEWMPPLAGATSALAKESASAINITLNGSQRVVASGVPDAYRMPAF 395
             CA CH   G+G+P     + G T+   ++  + + +  +G      SG      MP F
Sbjct: 306 NVCAGCHAPGGEGKPHIAVAMRGNTTLRLEDPRNLVRVIDDGIGEQKFSGFEHMQPMPGF 365

Query: 396 REQLSDTEIAEVLSYVRSTWGNNGGAVDANAVGKLRGHTDP 436
            ++L+D ++ ++L+Y+R  WG     +  N V KLR    P
Sbjct: 366 VDKLNDEQLTDLLNYLRQGWGGQPNDLAVNDVQKLRADAPP 406


Lambda     K      H
   0.318    0.133    0.423 

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: 559
Number of extensions: 32
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: 447
Length of database: 412
Length adjustment: 32
Effective length of query: 415
Effective length of database: 380
Effective search space:   157700
Effective search space used:   157700
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.

Links

Downloads

Related tools

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