GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ2 in Amphritea japonica JAMM 1866

Align Beta-ketoadipyl-CoA thiolase; 3-oxoadipyl-CoA thiolase; EC 2.3.1.174 (characterized)
to candidate WP_019620367.1 G329_RS0102470 beta-ketothiolase BktB

Query= SwissProt::Q8VPF1
         (401 letters)



>NCBI__GCF_000381785.1:WP_019620367.1
          Length = 394

 Score =  299 bits (765), Expect = 1e-85
 Identities = 177/399 (44%), Positives = 240/399 (60%), Gaps = 8/399 (2%)

Query: 3   REVYICDAVRTPIGRFGGSLAAVRADDLAAVPVKALVERNPQVDWSQLDEVYLGCANQAG 62
           REV +   VRT IG FGGSL +    +LA   V   V R+          V+    +   
Sbjct: 4   REVVVLSGVRTAIGGFGGSLKSQTPCELATTCVSEAVSRSGAAAEDFGHSVFGNVIHTER 63

Query: 63  EDNRNVARMALLLAGLPDSVPGVTLNRLCASGMDAVGTAFRAIASGEAELVIAGGVESMS 122
            D   + R+A +  GLP   PGVT+NRLC SG+ A+ +A + I  G  +  +AGG E MS
Sbjct: 64  RD-MYLGRVAAVNGGLPHETPGVTINRLCGSGLQAIISATQQIELGVCDAAVAGGSEVMS 122

Query: 123 RAPYVMGKADSAFGRGQKIEDTTIGWRFINPLMKAQYGVDAMPETADNVADDYKVSRADQ 182
           ++ Y M  A      GQ++ D  I    +  L    +    M  TA+N+AD ++VSR DQ
Sbjct: 123 KSQYWMPTARF----GQRMGDGAIVDAMVGALT-CPFDDTHMGITAENIADKWQVSREDQ 177

Query: 183 DAFALRSQQLAGRAQAAGYFAEEIVPVVIKGKKGETVVDADEHLRPDTTLEALAKLKPVN 242
           DA A+ S   A RA   G F E+IVP+ +K +KG TV D DEHLR   T   + KL+P  
Sbjct: 178 DALAVMSHNNAERAITEGRFKEQIVPIELKSRKGVTVFDTDEHLRYGCTTADMEKLRPAF 237

Query: 243 GPDKTVTAGNASGVNDGSVALILASAEAVKKHGLKARAKVLGMASAGVAPRVMGIGPVPA 302
             D +VTAGNASG+ND + A+ L +AE  +  GLK  A+++G + AGV P+ MGIGPVPA
Sbjct: 238 KRDGSVTAGNASGLNDAAAAVTLMAAETAEAKGLKPMARLVGYSFAGVEPKYMGIGPVPA 297

Query: 303 VRKLLERLNLSVADFDVIELNEAFAAQGLAVTRELGIADDDARVNPNGGAIALGHPLGAS 362
           VRKLL    LS+ D DV E+NEAFAAQ LAV R+L +  +  +VN NG  I+LGHP+GA+
Sbjct: 298 VRKLLADAELSIGDIDVWEVNEAFAAQALAVCRDLELPLE--KVNVNGSGISLGHPIGAT 355

Query: 363 GARLVLTAVHQLEKSGGQRGLCTMCVGVGQGVALAVERV 401
           GA + + A+H+L++SGG+  + TMC+G GQG+A   ERV
Sbjct: 356 GAIITVKALHELQRSGGRYAVVTMCIGGGQGIAALFERV 394


Lambda     K      H
   0.317    0.134    0.379 

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: 16
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: 401
Length of database: 394
Length adjustment: 31
Effective length of query: 370
Effective length of database: 363
Effective search space:   134310
Effective search space used:   134310
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: 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