GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Sinorhizobium meliloti 1021

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109) (characterized)
to candidate SMc00728 SMc00728 electron transfer flavoprotein alpha-subunit alpha-ETF flavoprotein

Query= BRENDA::Q18AQ5
         (336 letters)



>FitnessBrowser__Smeli:SMc00728
          Length = 309

 Score =  161 bits (408), Expect = 2e-44
 Identities = 113/326 (34%), Positives = 175/326 (53%), Gaps = 32/326 (9%)

Query: 4   VLVVIEQRENVIQTVSLELLGKATEIAKDYDTKVSALLLGSKVEGLIDTLAHY-GADEVI 62
           +L++ +   + +   + + L  A +I  D    V  L+ G  V+G+ +  +   G  +V+
Sbjct: 3   ILLLADHDNSHLSDQTAKALTAAAKIGGD----VHVLVAGQNVKGIAEQASKLSGVAKVL 58

Query: 63  VVDDEALAVYTTEPYTKAAYEAIKAADPIVVLFGATSIGRDLAPRVSARIHTGLTADCTG 122
           V +D +LA    EP   AA     A +   V+  ATS+G+++ PRV+A +     ++   
Sbjct: 59  VAEDASLANNLAEPL--AALIVSLAGNYDTVVAAATSVGKNVMPRVAALLDVAQVSEIIE 116

Query: 123 LAVAEDTKLLLMTRPAFGGNIMATIVCKDFRPQ-MSTVRPGVMKKNE-----PDETKEAV 176
           +  A+  +     RP + GN + T+   +  PQ + TVR       +     P ET  A 
Sbjct: 117 VVSADTYR-----RPIYAGNAIQTVQTSE--PQKVITVRTASFAAAQEGGSAPVETVAAA 169

Query: 177 INR-FKVEFNDADKLVQVVQVIKEAKKQVKIEDAKILVSAGRGMGGKENL-DILYELAEI 234
            N       +DA            +  + ++  AKI++S GR +G  E   +++  +A+ 
Sbjct: 170 ANPGLSAHVSDA----------LSSSDRPELTSAKIIISGGRALGSSEKFKEVILPVADK 219

Query: 235 IGGEVSGSRATIDAGWLDKARQVGQTGKTVRPDLYIACGISGAIQHIAGMEDAEFIVAIN 294
           +G  V  SRA +DAG+     QVGQTGK V PDLYIACGISGAIQH+AGM+D++ IVAIN
Sbjct: 220 LGAAVGASRAAVDAGYAPNDWQVGQTGKVVAPDLYIACGISGAIQHLAGMKDSKVIVAIN 279

Query: 295 KNPEAPIFKYADVGIVGDVHKVLPEL 320
           K+ EAPIF+ AD G+V D+ +VLPEL
Sbjct: 280 KDEEAPIFQVADYGLVADLFEVLPEL 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: 267
Number of extensions: 15
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: 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 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