GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Stutzerimonas stutzeri A1501

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109) (characterized)
to candidate WP_011913714.1 PST_RS13060 FAD-binding protein

Query= BRENDA::Q18AQ5
         (336 letters)



>NCBI__GCF_000013785.1:WP_011913714.1
          Length = 309

 Score =  161 bits (408), Expect = 2e-44
 Identities = 116/323 (35%), Positives = 171/323 (52%), Gaps = 26/323 (8%)

Query: 4   VLVVIEQRENVIQTVSLELLGKATEIAKDYDTKVSALLLGSKVEGLIDTLAHY-GADEVI 62
           +LV+ E    V+   +L  +  A  I  D    +  L+ GS    + +  A   G  +V+
Sbjct: 3   ILVIAEHNNAVLAAATLNTVAAAKAIGGD----IHVLVAGSGCGAIGEAAAQIEGVAKVL 58

Query: 63  VVDDEALAVYTTE-PYTKAAYEAIKAADPIVVLFGATSIGRDLAPRVSARIHTGLTADCT 121
           V DD   A YT + P   A   A  A +   VL  AT+ G++  PRV+A++     ++  
Sbjct: 59  VADD---AAYTNQLPENVAPLIADLAKNYSHVLAAATTNGKNFLPRVAAQLDVDQISEII 115

Query: 122 GLAVAEDTKLLLMTRPAFGGNIMATIVCKDFRPQMSTVRPGVMKKNEPDETKEAVINRFK 181
            +   +  K     RP + GN +AT+       Q S     +  ++   +   A      
Sbjct: 116 SVESPDTFK-----RPIYAGNAIATV-------QSSAPIKVITVRSTGFDAVNATGGSAA 163

Query: 182 VE----FNDADKLVQVVQVIKEAKKQVKIEDAKILVSAGRGMGGKENLDILYELAEIIGG 237
           VE      DA K   V + + ++ +  ++  AKI+VS GRGM   +N   LY LA+ +G 
Sbjct: 164 VEQISGTGDAGKSAFVGEELAKSDRP-ELTAAKIVVSGGRGMQNGDNFKHLYSLADKLGA 222

Query: 238 EVSGSRATIDAGWLDKARQVGQTGKTVRPDLYIACGISGAIQHIAGMEDAEFIVAINKNP 297
            V  SRA +DAG++    QVGQTGK V P LYIA GISGAIQH+AGM+D++ IVAINK+ 
Sbjct: 223 AVGASRAAVDAGFVPNDMQVGQTGKIVAPQLYIAVGISGAIQHLAGMKDSKVIVAINKDE 282

Query: 298 EAPIFKYADVGIVGDVHKVLPEL 320
           EAPIF+ AD G+VGD+ +++PEL
Sbjct: 283 EAPIFQVADYGLVGDLFEIIPEL 305


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: 280
Number of extensions: 8
Number of successful extensions: 1
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: 309
Length adjustment: 28
Effective length of query: 308
Effective length of database: 281
Effective search space:    86548
Effective search space used:    86548
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 Apr 09 2024. 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