GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Sedimenticola selenatireducens DSM 17993

Align Beta-ketothiolase BktB; Acetyl-CoA acetyltransferase; Acetyl-CoA acyltransferase; EC 2.3.1.16; EC 2.3.1.9 (characterized)
to candidate WP_029132922.1 A3GO_RS0107785 acetyl-CoA C-acyltransferase

Query= SwissProt::Q0KBP1
         (394 letters)



>NCBI__GCF_000428045.1:WP_029132922.1
          Length = 395

 Score =  506 bits (1303), Expect = e-148
 Identities = 258/392 (65%), Positives = 306/392 (78%), Gaps = 1/392 (0%)

Query: 3   REVVVVSGVRTAIGTFGGSLKDVAPAELGALVVREALARAQVSGDDVGHVVFGNVIQTEP 62
           +E+VV+S VRTA+G++GG LKDV   +L A V+R A+ R+ V+  DVGH V G+VI TEP
Sbjct: 5   KEIVVLSAVRTAVGSYGGGLKDVPVVDLAATVIRAAVERSGVAPADVGHTVLGHVIHTEP 64

Query: 63  RDMYLGRVAAVNGGVTINAPALTVNRLCGSGLQAIVSAAQTILLGDTDVAIGGGAESMSR 122
           RDMY+ R A+V GG+ +  PA T+NRLCGSGLQAIVSA Q I  G  DVA+ GGAE+MSR
Sbjct: 65  RDMYISRYASVTGGLPVETPAFTLNRLCGSGLQAIVSAVQQIETGHCDVAVAGGAENMSR 124

Query: 123 APYLAPAARWGARMGDAGLVDMMLGALHDPFHRIHMGVTAENVAKEYDISRAQQDEAALE 182
           A YLAP+ RWGARM DA +VDMM+GAL DPF  IHMGVTAEN+A+++ ISR +QD  A+E
Sbjct: 125 AGYLAPSLRWGARMSDAQIVDMMVGALTDPFEGIHMGVTAENIAEKWGISREEQDALAVE 184

Query: 183 SHRRASAAIKAGYFKDQIVPVVSKGRKGDVTFDTDEHVRHDATIDDMTKLRPVFVKENGT 242
           SHRRA+ A + GYFKDQIVPV  K RKG   F+ DEH R DA +  M KLRPVF KE G+
Sbjct: 185 SHRRAAQAWEKGYFKDQIVPVELKSRKGTTLFERDEHFRADANLAGMAKLRPVFKKE-GS 243

Query: 243 VTAGNASGLNDAAAAVVMMERAEAERRGLKPLARLVSYGHAGVDPKAMGIGPVPATKIAL 302
           VTAGNASGLNDAA+AVV+     AE +GLKPLARLV Y HAG +P  MGIGPVPA K  L
Sbjct: 244 VTAGNASGLNDAASAVVVATAEYAESKGLKPLARLVGYSHAGCEPAYMGIGPVPAVKRLL 303

Query: 303 ERAGLQVSDLDVIEANEAFAAQACAVTKALGLDPAKVNPNGSGISLGHPIGATGALITVK 362
           +R GL+V+D DV+E NEAFAAQA AV + LGL   + NPNGSGISLGHPIGATG+++T K
Sbjct: 304 DRTGLKVADFDVLEVNEAFAAQAIAVCRDLGLPMDRTNPNGSGISLGHPIGATGSIVTTK 363

Query: 363 ALHELNRVQGRYALVTMCIGGGQGIAAIFERI 394
           A+HEL+R  GRYALVTMCIGGGQGIAA FERI
Sbjct: 364 AIHELHRSGGRYALVTMCIGGGQGIAAAFERI 395


Lambda     K      H
   0.318    0.134    0.381 

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: 493
Number of extensions: 11
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: 394
Length of database: 395
Length adjustment: 31
Effective length of query: 363
Effective length of database: 364
Effective search space:   132132
Effective search space used:   132132
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 (21.7 bits)
S2: 50 (23.9 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