GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Desulfoscipio geothermicus DSM 3669

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; EC 2.3.1.9 (characterized)
to candidate WP_092481563.1 BM299_RS00825 acetyl-CoA C-acetyltransferase

Query= SwissProt::P45855
         (393 letters)



>NCBI__GCF_900115975.1:WP_092481563.1
          Length = 392

 Score =  502 bits (1292), Expect = e-147
 Identities = 258/391 (65%), Positives = 301/391 (76%), Gaps = 2/391 (0%)

Query: 3   KTVIVSAARTPFGKFGGVLKEVKAAELGGIVMKEALQQAGV-SGDDVEGNVMGMVVQAGS 61
           KTVIVSA RTPFGK GG L  +KA +LGGIV+KEAL +AG+ +G  V+  +MG V+Q G 
Sbjct: 2   KTVIVSAVRTPFGKLGGKLSSIKATKLGGIVIKEALNRAGLGNGAIVDNVIMGQVLQGGC 61

Query: 62  GQIPSRQAARLAGMPWSVPSETLNKVCASGLRAVTLCDQMIRAQDADILVAGGMESMSNI 121
           GQIPSRQA R AGMPW VPSETLNKVCASGLR+VT+ DQMIR  DADI+VAGGMESMSN 
Sbjct: 62  GQIPSRQATREAGMPWEVPSETLNKVCASGLRSVTMGDQMIRCGDADIIVAGGMESMSNA 121

Query: 122 PYAVPAGRWGARMGDGELRDLMVYDGLTCAFDEVHMAVHGNTAAKEYAISRREQDEWALR 181
           PY     RWG RMGDG+L DLMV+DGL CAF   HM +HG   AKEY +SR EQDEWALR
Sbjct: 122 PYFGNC-RWGLRMGDGKLVDLMVHDGLWCAFYNRHMGIHGGVVAKEYGVSREEQDEWALR 180

Query: 182 SHARAAKAADEGKFQDEIVPVNWIGRKGKPNVVDKDEAIRRDTSLDQLAKLAPIYASDGS 241
           SH  A KA D GK ++EI+ V    +KG P VVD DE  RRDTS+++L KL P++  + +
Sbjct: 181 SHEFAIKAIDSGKLKEEIISVPIPQKKGDPLVVDTDEGPRRDTSMEKLRKLPPVFDPENT 240

Query: 242 ITAGNAPGVNDGAGAFVLMSEEKAAELGKRPLATILGFSTTGMPAHELAAAPGFAINKLL 301
           +TAGNAPG+NDGAGA V+MSEE A ELG +PLATILG ++    A  +A  PG +INKLL
Sbjct: 241 VTAGNAPGINDGAGALVIMSEETAKELGLKPLATILGHASVSQEASYIATVPGLSINKLL 300

Query: 302 KKNGLTVQDIDLFEVNEAFASVVLTCEKIVGFDLEKVNVNGGAIALGHPIGASGARILMT 361
           +K  L +  IDLFEVNEAFA+V L   KI  +D  KVNVNGGA+A GHPIGASGARILM 
Sbjct: 301 QKEHLNINQIDLFEVNEAFAAVTLVSGKICNWDSNKVNVNGGAVAYGHPIGASGARILMA 360

Query: 362 LVYELKRRGGGLGVAAICSGAAQGDAVLVQV 392
           L YEL+RRGGGLGVAAICSGAAQGDAVL++V
Sbjct: 361 LAYELRRRGGGLGVAAICSGAAQGDAVLIKV 391


Lambda     K      H
   0.317    0.134    0.387 

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: 565
Number of extensions: 17
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: 393
Length of database: 392
Length adjustment: 31
Effective length of query: 362
Effective length of database: 361
Effective search space:   130682
Effective search space used:   130682
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 Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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