GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etfA in Collinsella tanakaei YIT 12063

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109) (characterized)
to candidate WP_009142158.1 HMPREF9452_RS10730 4Fe-4S dicluster domain-containing protein

Query= BRENDA::Q18AQ5
         (336 letters)



>NCBI__GCF_000225705.1:WP_009142158.1
          Length = 408

 Score =  226 bits (577), Expect = 6e-64
 Identities = 131/309 (42%), Positives = 183/309 (59%), Gaps = 2/309 (0%)

Query: 18  VSLELLGKATEIAKDYDTKVSALLL--GSKVEGLIDTLAHYGADEVIVVDDEALAVYTTE 75
           V+ ELLG+A E+A     +V ALL    +  +     L   GADEV++  D+ LA     
Sbjct: 98  VAFELLGRARELAAIRGCRVVALLGQGATAPQDQAPALLAAGADEVLLCRDDRLATLDAR 157

Query: 76  PYTKAAYEAIKAADPIVVLFGATSIGRDLAPRVSARIHTGLTADCTGLAVAEDTKLLLMT 135
            Y     +      P ++L+GAT+ GR+LAP V+ R+ TGLTADCT L +   T LL  T
Sbjct: 158 VYAHWICDMAGERKPEIILYGATAFGRELAPGVAVRLQTGLTADCTVLDIDPATGLLQQT 217

Query: 136 RPAFGGNIMATIVCKDFRPQMSTVRPGVMKKNEPDETKEAVINRFKVEFNDADKLVQVVQ 195
           RPAFGGN+MATI C   RPQM+TVRPG+    + D          +V   DA +    V 
Sbjct: 218 RPAFGGNLMATIECPRHRPQMATVRPGIFAAPQVDALHAERGRITQVALADAWRPSVRVD 277

Query: 196 VIKEAKKQVKIEDAKILVSAGRGMGGKENLDILYELAEIIGGEVSGSRATIDAGWLDKAR 255
            I+ A     I DA +LV AGRG+G K+NL +   LA+++GG++  +R  +++GWL+   
Sbjct: 278 AIEHAGATDIITDADVLVVAGRGIGSKKNLAVAQRLADVLGGKLGCTRPLVESGWLEYWH 337

Query: 256 QVGQTGKTVRPDLYIACGISGAIQHIAGMEDAEFIVAINKNPEAPIFKYADVGIVGDVHK 315
           QVGQTG +V P L I+ G+SGAIQH+AG   A  ++A+N++P APIF  A   +VGD  +
Sbjct: 338 QVGQTGVSVSPKLLISLGVSGAIQHVAGTGGARTVIAVNEDPNAPIFGSATYRVVGDCVE 397

Query: 316 VLPELISQL 324
           V  EL ++L
Sbjct: 398 VARELTARL 406


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: 387
Number of extensions: 19
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: 408
Length adjustment: 30
Effective length of query: 306
Effective length of database: 378
Effective search space:   115668
Effective search space used:   115668
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