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_092487318.1 BM299_RS17115 acetyl-CoA C-acetyltransferase

Query= SwissProt::Q0AVM3
         (396 letters)



>NCBI__GCF_900115975.1:WP_092487318.1
          Length = 393

 Score =  397 bits (1019), Expect = e-115
 Identities = 203/394 (51%), Positives = 274/394 (69%), Gaps = 7/394 (1%)

Query: 3   REVVLVGACRTPVGTFGGTLKDVGSAQLGAIVMGEAIKRAGIKAEQIDEVIFGCVLQAGL 62
           ++VV+V   RTP+G FGG L+ V + QL  +V+ E IKR G+   +ID+VI GC +Q+  
Sbjct: 2   KDVVIVAGARTPIGDFGGALRSVTAGQLAVVVIKEVIKRTGVNPAEIDDVILGCCVQSSE 61

Query: 63  GQNVARQCMINAGIPKEVTAFTINKVCGSGLRAVSLAAQVIKAGDADIIMAGGTENMDKA 122
             N+ R   + AG+P  VT  TI + C SG++A+    Q I  GD++I++AGGTE+M  A
Sbjct: 62  EPNIGRTAALMAGLPDNVTGMTIQRQCASGMQAIISGYQQIITGDSEIVLAGGTESMSTA 121

Query: 123 PFILPNARWGYRMSMPKGDLIDEMVWGGLTDVFNGYHMGITAENINDMYGITREEQDAFG 182
           P++L  ARWG R+    G+  D + W  LTD  +   MG TAE + D YGITREEQD   
Sbjct: 122 PYVLKKARWGMRLQ--HGEFTDAL-WETLTDPIHKIMMGETAERLADKYGITREEQDIIA 178

Query: 183 FRSQTLAAQAIESGRFKDEIVPVVIKGKKGDIVF-DTDEHPRKS-TPEAMAKLAPAFKKG 240
           +RS   A  AIE G F  EIVPV +  +KGD+V  D DEHPR   + E +AKL+PAF+K 
Sbjct: 179 YRSHQNAINAIEKGYFAGEIVPVPVPRRKGDLVLVDRDEHPRNDISMEKLAKLSPAFRKN 238

Query: 241 GSVTAGNASGINDAAAAVIVMSKEKADELGIKPMAKVVSYASGGVDPSVMGLGPIPASRK 300
           G+VTAGNASG+NDAAA V++MS+EKA +LG+KP+A++VS+A  GV+P +MG GP+PA +K
Sbjct: 239 GTVTAGNASGLNDAAAGVLLMSEEKARQLGLKPLARIVSHARAGVEPDLMGYGPVPAIKK 298

Query: 301 ALEKAGLTIDDIDLIEANEAFAAQSIAVARDLGWADKMEKVNVNGGAIAIGHPIGSSGAR 360
           AL++AGL + DIDLIE NEAFAAQ +A  + L      E VNVNG  + +GHP+G +G R
Sbjct: 299 ALQRAGLALADIDLIELNEAFAAQYLACEKLLDL--NREIVNVNGSGVGLGHPVGCTGTR 356

Query: 361 ILVTLLYEMQKRGSKKGLATLCIGGGMGTALIVE 394
           I+VTLL EM++R +  GLA+LC+GGGMG A+IVE
Sbjct: 357 IVVTLLNEMERRNAHYGLASLCVGGGMGVAVIVE 390


Lambda     K      H
   0.317    0.135    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: 494
Number of extensions: 19
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: 396
Length of database: 393
Length adjustment: 31
Effective length of query: 365
Effective length of database: 362
Effective search space:   132130
Effective search space used:   132130
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.

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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