GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Marinobacter adhaerens HP15

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109) (characterized)
to candidate GFF1797 HP15_1755 electron transfer flavoprotein subunit alpha

Query= BRENDA::Q18AQ5
         (336 letters)



>FitnessBrowser__Marino:GFF1797
          Length = 313

 Score =  165 bits (417), Expect = 2e-45
 Identities = 112/332 (33%), Positives = 175/332 (52%), Gaps = 34/332 (10%)

Query: 3   NVLVVIEQRENVIQTVSLELLGKATEIAKDYDTKVSALLLGSKVEGLIDTLAHYGADEVI 62
           ++LV+ E   + ++  +L ++  A  I  D D  V+    G+  E  +      G ++V+
Sbjct: 2   SILVIAEHDNSSLKQATLNVVAAAKAIGGDIDVLVAGENCGAVAEAAVKA---EGVNKVL 58

Query: 63  VVDDEALAVYTTEPYTKAAYEAIKAADPIVVLFGATSIGRDLAPRVSARIHTGLTADCTG 122
           V D+ A   +  E   +   E  K    I+   G  ++G+D  PRV+A +     +D   
Sbjct: 59  VADNAAYGHFLGENLGELVAEVGKGYSHILAAAG--TVGKDFMPRVAALLDVAQVSDIMR 116

Query: 123 LAVAEDTKLLLMTRPAFGGNIMATIVCKDFRPQMSTVRP----------GVMKKNEPDET 172
           +  +EDT      RP + GN +AT+   D   ++ TVRP          G     + D  
Sbjct: 117 VE-SEDT----FVRPIYAGNAIATVKSSD-SIKVVTVRPTAFDPVAAEGGSASVEQLDVV 170

Query: 173 KEAVINRFKVEFNDADKLVQVVQVIKEAKKQVKIEDAKILVSAGRGMGGKENLDILYELA 232
           K+A +++F  E           ++ K  +    +  A I+VS GRGM   +N  +L ++A
Sbjct: 171 KDAGLSQFVSE-----------ELAKSDRPD--LASAGIVVSGGRGMQNGDNFKMLEQVA 217

Query: 233 EIIGGEVSGSRATIDAGWLDKARQVGQTGKTVRPDLYIACGISGAIQHIAGMEDAEFIVA 292
           +++G  V  SRA +DAG++    QVGQTGK V P LYIA GISGAIQH+AGM D++ IVA
Sbjct: 218 DLMGAAVGASRAAVDAGFVPNDMQVGQTGKIVAPQLYIAVGISGAIQHLAGMSDSKVIVA 277

Query: 293 INKNPEAPIFKYADVGIVGDVHKVLPELISQL 324
           INK+ EAPIF+ AD G+V D+ + +P+L  +L
Sbjct: 278 INKDEEAPIFQVADYGLVADLFEAVPQLEEEL 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: 277
Number of extensions: 14
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: 336
Length of database: 313
Length adjustment: 28
Effective length of query: 308
Effective length of database: 285
Effective search space:    87780
Effective search space used:    87780
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