GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Paraburkholderia bryophila 376MFSha3.1

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109) (characterized)
to candidate H281DRAFT_03367 H281DRAFT_03367 electron transfer flavoprotein alpha subunit apoprotein

Query= BRENDA::Q18AQ5
         (336 letters)



>FitnessBrowser__Burk376:H281DRAFT_03367
          Length = 314

 Score =  155 bits (391), Expect = 2e-42
 Identities = 110/318 (34%), Positives = 164/318 (51%), Gaps = 17/318 (5%)

Query: 5   LVVIEQRENVIQTVSLELLGKATEIAKDYDTKVSALLLGSKVEGLIDTLAHY-GADEVIV 63
           LV+ E     I+  +L  +  A ++  D    +  L+ G   +   D  A   G  +V++
Sbjct: 7   LVIAEHDNTSIKGATLNTIAAAQKVGGD----IHVLVAGQNAQAAADAAAKIAGVSKVLL 62

Query: 64  VDDEALAVYTTEPYTKAAYEAIKAADPIVVLFGATSIGRDLAPRVSARIHTGLTADCTGL 123
            D   LA    E          K  D   +   AT+ G+++APR++A++     +D T +
Sbjct: 63  ADAPQLAEGLAENVEATVLNIAK--DYSHIFAPATAYGKNIAPRIAAKLDVAQISDITAV 120

Query: 124 AVAEDTKLLLMTRPAFGGNIMATIVCKDFRPQMSTVRPGVMKKNEPDETKEAVINRFKVE 183
             + DT      RP + GN +AT+   D   ++ TVR         +     V    K+E
Sbjct: 121 D-SPDT----FERPIYAGNAIATVQSAD-PIKVITVRTTGFDAVAAEGGNATVE---KIE 171

Query: 184 FNDADKLVQVVQVIKEAKKQVKIEDAKILVSAGRGMGGKENLD-ILYELAEIIGGEVSGS 242
                 + Q V        + ++  AKI+VS GRG+G  EN   +L  LA+ +   +  S
Sbjct: 172 AAADAGISQFVSREVTKLDRPELTSAKIIVSGGRGLGNGENYTKVLEPLADKLNAALGAS 231

Query: 243 RATIDAGWLDKARQVGQTGKTVRPDLYIACGISGAIQHIAGMEDAEFIVAINKNPEAPIF 302
           RA +DAG++    QVGQTGK V P LY+A GISGAIQH+AGM+D++ IVAINK+PEAPIF
Sbjct: 232 RAAVDAGFVPNDYQVGQTGKIVAPQLYVAVGISGAIQHLAGMKDSKVIVAINKDPEAPIF 291

Query: 303 KYADVGIVGDVHKVLPEL 320
             AD G+VGD+  ++PEL
Sbjct: 292 SVADYGLVGDLFTLVPEL 309


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: 266
Number of extensions: 15
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: 336
Length of database: 314
Length adjustment: 28
Effective length of query: 308
Effective length of database: 286
Effective search space:    88088
Effective search space used:    88088
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: 48 (23.1 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