GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Lentibacillus jeotgali Grbi

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109) (characterized)
to candidate WP_010532456.1 ON01_RS18190 electron transfer flavoprotein subunit alpha/FixB family protein

Query= BRENDA::Q18AQ5
         (336 letters)



>NCBI__GCF_000224785.1:WP_010532456.1
          Length = 321

 Score =  214 bits (546), Expect = 2e-60
 Identities = 122/322 (37%), Positives = 193/322 (59%), Gaps = 8/322 (2%)

Query: 4   VLVVIEQRENVIQTVSLELLGKATEIAKDYDTKVSALLLGSK-VEGLIDTLAHYGADEVI 62
           +LV+ E R+  ++ V+ E +  A +I  D D ++  +L GS  +      + ++GAD V+
Sbjct: 3   LLVIGEARDGELRNVTFEAVAAAKKI--DSDAEIVGVLCGSDDLNESGQEVIYHGADRVV 60

Query: 63  VVDDEALAVYTTEPYTKAAYEAIKAADPIVVLFGATSIGRDLAPRVSARIHTGLTADCTG 122
            V  + L  YT+E Y++A    I+   P  ++ G T+IG+DL P+++A++ TGL +D T 
Sbjct: 61  TVTHDNLESYTSEGYSQAVMAVIEDESPDGIVMGHTAIGKDLTPKLAAKLGTGLISDATD 120

Query: 123 LAVAEDTKLLLMTRPAFGGNIMATIVCKDFRPQMSTVRPGVMKKNEPDETKEAVINRFKV 182
             +  D    + TRP + G      V        +T+RP  +   E D ++   +   +V
Sbjct: 121 --IENDGDKAVFTRPIYSGKAFEKKVMTSGLT-FATIRPNNIPALERDASRSGDVTSKEV 177

Query: 183 EFNDADKLVQVVQVIKEAKKQVKIEDAKILVSAGRGMGGKENLDILYELAEIIGGEVSGS 242
           +  D + +++   VI++A + V + +A ++V+ GRG+   E  + LYELA+I+GG V  S
Sbjct: 178 DVKDINTVIK--DVIRKASEGVDLSEANVIVAGGRGVKSAEGFEPLYELADILGGAVGAS 235

Query: 243 RATIDAGWLDKARQVGQTGKTVRPDLYIACGISGAIQHIAGMEDAEFIVAINKNPEAPIF 302
           R   DA + D + Q+GQTGK V PDLYIA GISGAIQH+AGM +++ IVAINK+PEA IF
Sbjct: 236 RGACDAEYCDYSLQIGQTGKVVTPDLYIAVGISGAIQHLAGMSNSKVIVAINKDPEANIF 295

Query: 303 KYADVGIVGDVHKVLPELISQL 324
             AD GIVGD+ +V+P+L  +L
Sbjct: 296 NVADYGIVGDIFEVIPKLTEEL 317


Lambda     K      H
   0.316    0.135    0.371 

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: 291
Number of extensions: 13
Number of successful extensions: 2
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: 336
Length of database: 321
Length adjustment: 28
Effective length of query: 308
Effective length of database: 293
Effective search space:    90244
Effective search space used:    90244
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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