GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Sinorhizobium meliloti 1021

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 3/3) (EC 1.3.1.109); short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate SM_b20753 SM_b20753 acyl-CoA dehydrogenase

Query= BRENDA::Q18AQ1
         (378 letters)



>FitnessBrowser__Smeli:SM_b20753
          Length = 380

 Score =  290 bits (743), Expect = 3e-83
 Identities = 152/374 (40%), Positives = 231/374 (61%), Gaps = 3/374 (0%)

Query: 5   SKKYQMLKELYVSFAENEVKPLATELDEEERFPYETVEKMAKAGMMGIPYPKEYGGEGGD 64
           S++ + ++ + + FA +E+ P A + D+++ FP ET+   A  GM GI    + GG G  
Sbjct: 6   SEEQEAIRTMALDFARDEIAPHAVDWDQQKHFPVETLRAAAALGMAGIYIRDDVGGTGLT 65

Query: 65  TVGYIMAVEELSRVCGTTGVILSAHTSLGSWPIYQYGNEEQKQKFLRPLASGEKLGAFGL 124
            +   M +E L+  C      +S H       I +YG +EQ+++ L PL + + L ++ L
Sbjct: 66  RLDAAMIIEALATGCPAIASFVSIHNMCAGM-IDRYGTDEQRRRLLPPLLTMDVLASYCL 124

Query: 125 TEPNAGTDASGQQTTAVLDGDEYILNGSKIFITNAIAGDIYVVMAMTDKSKGNKGISAFI 184
           TEP +G+DA+  +T AV +GD Y+L G K FI+ A    +Y+VMA T + +G KGISAF+
Sbjct: 125 TEPGSGSDAAALKTRAVREGDAYLLTGQKQFISGAGESGLYIVMARTGE-EGPKGISAFV 183

Query: 185 VEKGTPGFSFGVKEKKMGIRGSATSELIFEDCRIPKENLLGKEGQGFKIAMSTLDGGRIG 244
           VEK  PG +FG  EKKMG     T  ++ ++ R+  EN LG EG+GF+IAM+ LDGGR+ 
Sbjct: 184 VEKDAPGLTFGANEKKMGWHAQPTRAVMLDNVRVSVENRLGAEGEGFRIAMAGLDGGRLS 243

Query: 245 IAAQALGLAQGALDETVKYVKERVQFGRPLSKFQNTQFQLADMEVKVQAARHLVYQAAIN 304
           IAA +LG AQ A D+ + YV+ER  FG+ + +FQ  QF+LADM   ++ AR  +++AA  
Sbjct: 244 IAAASLGGAQSAFDKALAYVQERRAFGKAIGEFQALQFRLADMATDLEIARTFLWRAACA 303

Query: 305 KDLGKPYGVE-AAMAKLFAAETAMEVTTKAVQLHGGYGYTRDYPVERMMRDAKITEIYEG 363
            D   P   +  AMAK F  +    V   A+QLHGGYGY  DY VE+++RD ++ +I EG
Sbjct: 304 LDAADPEATKLCAMAKRFVTDRCFSVANDALQLHGGYGYLADYGVEKIVRDLRVHQILEG 363

Query: 364 TSEVQRMVISGKLL 377
           T+E+ R+++S  ++
Sbjct: 364 TNEIMRLIVSRAIM 377


Lambda     K      H
   0.315    0.133    0.373 

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: 308
Number of extensions: 16
Number of successful extensions: 4
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: 378
Length of database: 380
Length adjustment: 30
Effective length of query: 348
Effective length of database: 350
Effective search space:   121800
Effective search space used:   121800
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: 42 (22.0 bits)
S2: 50 (23.9 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