GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Mucilaginibacter gossypiicola Gh-48

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109) (characterized)
to candidate WP_091206026.1 BMX50_RS00255 electron transfer flavoprotein subunit alpha/FixB family protein

Query= BRENDA::Q18AQ5
         (336 letters)



>NCBI__GCF_900110105.1:WP_091206026.1
          Length = 325

 Score =  184 bits (467), Expect = 3e-51
 Identities = 118/326 (36%), Positives = 170/326 (52%), Gaps = 5/326 (1%)

Query: 3   NVLVVIEQRENVIQTVSLELLGKATEIAKDYDTKVSALLLGSKVEGLIDTLAHYGADEVI 62
           +VL+  E      +    E +  A  IA   +T V+A+ +G+     +  L  YGAD+V+
Sbjct: 2   SVLIYAENAGGKFKKSIFEAVSYARAIADQSNTSVTAVSIGNVDATELALLGKYGADKVL 61

Query: 63  VVDDEALAVYTTEPYTKAAYEAIKAADPIVVLFGATSIGRDLAPRVSARIHTGLTADCTG 122
            V  + L  +  + Y     EA K     VV+   T  GR LAPRV  ++  G+      
Sbjct: 62  NVSGDKLKDFVNQAYASVIAEAAKKEGSAVVVLSNTFSGRGLAPRVGVKLEAGVADGAVA 121

Query: 123 LAVAEDTKLLLMTRPAFGGNIMATIVCKDFRPQMSTVRPGVMKKNEPDETKEAVINRFKV 182
           L         +  + AF G   AT+        ++ V P   K  E   T  A +  F V
Sbjct: 122 LPEQAGGSFKVK-KTAFSGKAFATVELTAAIKVIALV-PNSYKVVETGGT--AQVEDFNV 177

Query: 183 EFNDADKLVQVVQVIKEAKKQVKIEDAKILVSAGRGMGGKENLDILYELAEIIGGEVSGS 242
           E   +D    + ++++   K V + DA+I+VS GRG+ G EN  ++ ELAE++G   + S
Sbjct: 178 EPKASDFKAMIKEIVRSTDK-VSLPDAEIVVSGGRGLKGPENWGMIEELAELLGAATACS 236

Query: 243 RATIDAGWLDKARQVGQTGKTVRPDLYIACGISGAIQHIAGMEDAEFIVAINKNPEAPIF 302
           +   DAGW   +  VGQTG  V P+LYIA GISGAIQH+AG+  ++ IV INK+PEAP F
Sbjct: 237 KPVSDAGWRPHSEHVGQTGIAVSPNLYIAVGISGAIQHLAGVSSSKVIVVINKDPEAPFF 296

Query: 303 KYADVGIVGDVHKVLPELISQLSVAK 328
           K AD GIVGD  +VLP+LI+ +   K
Sbjct: 297 KVADYGIVGDAFEVLPKLIAAVKEYK 322


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: 284
Number of extensions: 12
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: 325
Length adjustment: 28
Effective length of query: 308
Effective length of database: 297
Effective search space:    91476
Effective search space used:    91476
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