GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Moritella dasanensis ArB 0140

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; EC 2.3.1.9 (characterized)
to candidate WP_017223438.1 A923_RS0119825 acetyl-CoA C-acyltransferase FadA

Query= SwissProt::Q0AVM3
         (396 letters)



>NCBI__GCF_000276805.1:WP_017223438.1
          Length = 389

 Score =  297 bits (760), Expect = 4e-85
 Identities = 177/401 (44%), Positives = 253/401 (63%), Gaps = 22/401 (5%)

Query: 3   REVVLVGACRTPVG-TFGGTLKDVGSAQLGAIVMGEAIKR-AGIKAEQIDEVIFGCVLQA 60
           R+VV+V   RTP+G +  G  + V +  L A +M   + R   +    I++V +GCV Q 
Sbjct: 2   RDVVVVDCLRTPMGRSKAGAFRHVRAEDLSAKLMRGLLDRNPEVDPNDIEDVYWGCVQQT 61

Query: 61  -GLGQNVARQCMINAGIPKEVTAFTINKVCGSGLRAVSLAAQVIKAGDADIIMAGGTENM 119
              G N+AR   + AGIP    A T+N++CGS ++A+  A + I  GD D+++ GG E+M
Sbjct: 62  LEQGFNIARNASLLAGIPITAGATTVNRLCGSSMQAIHDATRAIAMGDGDVMIIGGVEHM 121

Query: 120 DKAPFILPNARWGYRMSMPKGDLIDEMVWGGLTDVFNGYHMGITAENINDMYGITREEQD 179
              P    N    + + + K            T    G  MG+TAE +  M+GITRE+QD
Sbjct: 122 GHVPM---NHGVDFHVGLAKS-----------TAKAAGM-MGLTAEMLGKMHGITREQQD 166

Query: 180 AFGFRSQTLAAQAIESGRFKDEIVPVVIKGKKGDI-VFDTDEHPR-KSTPEAMAKLAPAF 237
           AF  RS  LA  A  SGRFK EI+P+      G + ++D DE  R ++T E++A L P F
Sbjct: 167 AFAVRSHKLAQAATVSGRFKREILPIEGHDADGILKLYDFDEVIRPETTMESLAGLRPVF 226

Query: 238 KK-GGSVTAGNASGINDAAAAVIVMSKEKADELGIKPMAKVVSYASGGVDPSVMGLGPIP 296
               G+VTAG +S ++D A+A+++MS +KA ELG+KP A+VVS A  G DPS+MG GP+P
Sbjct: 227 DPVNGTVTAGTSSALSDGASAMLLMSADKAKELGLKPRARVVSMAVAGCDPSIMGYGPVP 286

Query: 297 ASRKALEKAGLTIDDIDLIEANEAFAAQSIAVARDLGWADKME-KVNVNGGAIAIGHPIG 355
           A++KAL++AGLTI+DID+ E NEAFAAQS+   +DLG  D +E K+N+NGGAI++GHP+G
Sbjct: 287 ATKKALKRAGLTINDIDVFELNEAFAAQSLPCVKDLGLEDVVETKINLNGGAISLGHPLG 346

Query: 356 SSGARILVTLLYEMQKRGSKKGLATLCIGGGMGTALIVEAL 396
            SG+RI  TL+ E++ +G + GLAT+CIG G G A I E +
Sbjct: 347 CSGSRISTTLVNELEVQGGRYGLATMCIGLGQGIATIFERI 387


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: 443
Number of extensions: 23
Number of successful extensions: 5
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: 389
Length adjustment: 31
Effective length of query: 365
Effective length of database: 358
Effective search space:   130670
Effective search space used:   130670
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