GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Sinorhizobium meliloti 1021

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 2/3) (EC 1.3.1.109); short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate SMa0819 SMa0819 FixB electron transfer flavoprotein alpha chain

Query= BRENDA::D2RIQ3
         (340 letters)



>FitnessBrowser__Smeli:SMa0819
          Length = 353

 Score =  229 bits (583), Expect = 1e-64
 Identities = 129/324 (39%), Positives = 185/324 (57%), Gaps = 5/324 (1%)

Query: 13  KDLWVYVEHYKGEPVHVVYELLGECRKLADKCNQKLAAVLITDDAKDVPSKLIAR----G 68
           +++WV++E   G+   V  ELLGE RKLADK    LA V+I        +  IA     G
Sbjct: 13  RNVWVFIELEHGQVHPVSIELLGEGRKLADKLGVHLAGVVIGPPGGQGTANAIADAFAYG 72

Query: 69  ADLVYVCQDPAFKYYSTDEYTNAFCEMIDEYQPSSVFIGATNDGRDLGPRIAARVNTGLC 128
           ADL Y+ + P   +Y  + +T A  +++   +P  + +GAT  GRDL   +A  + TGL 
Sbjct: 73  ADLSYLVESPLLAHYRNEPFTKALTDLVLANKPEILLLGATTLGRDLAGSVATTLKTGLT 132

Query: 129 ADCTILDAEEDGLIEWTRPAAGGNIMATILCKEHRPQMGTVRPKTFKAMEPDASRTGEVI 188
           ADCT L+ + DG +  TRP  GG+++ TI   + RPQM TVRP      +     TG +I
Sbjct: 133 ADCTELNVDSDGSLAATRPTFGGSLLCTIYTLKCRPQMATVRPSVMATPQRVNRPTGSII 192

Query: 189 NYTLKNHVDDRVTCIRREEVVSEGEMA-IDDAPFVCSGGRGMKAKENFSLLYDLAHALGG 247
            + LK   ++  T +       +  +A +  A  V +GG G+ A +N  LL DLA  LGG
Sbjct: 193 RHDLKMLEEEIATKVLAFFSDCDSTIANLAYADVVVAGGLGLGAVQNLQLLKDLARTLGG 252

Query: 248 AVGGSRAAVDEGFIEHPRQVGQSGKTVTPKIYFACGISGSVQHKAGMSKSDTIVCINKDP 307
             G SR  V +G++   RQ+GQ+G T+ PK+Y A GISG+VQH+ G+  SD IV IN DP
Sbjct: 253 DFGCSRPLVQKGWMPFDRQIGQTGNTIRPKLYIAAGISGAVQHRVGVEGSDLIVAINTDP 312

Query: 308 DAPMFEISKYGIVGDALKILPLLT 331
           +AP+F+ +  G+V DA+  LP LT
Sbjct: 313 NAPIFDFAHLGVVADAISFLPALT 336


Lambda     K      H
   0.318    0.136    0.406 

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: 307
Number of extensions: 18
Number of successful extensions: 3
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: 340
Length of database: 353
Length adjustment: 29
Effective length of query: 311
Effective length of database: 324
Effective search space:   100764
Effective search space used:   100764
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: 49 (23.5 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