GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Cereibacter sphaeroides ATCC 17029

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; EC 2.3.1.9 (characterized)
to candidate WP_011842153.1 RSPH17029_RS16020 3-oxoadipyl-CoA thiolase

Query= SwissProt::Q0AVM3
         (396 letters)



>NCBI__GCF_000015985.1:WP_011842153.1
          Length = 399

 Score =  326 bits (836), Expect = 6e-94
 Identities = 179/396 (45%), Positives = 253/396 (63%), Gaps = 6/396 (1%)

Query: 4   EVVLVGACRTPVGTFGGTLKDVGSAQLGAIVMGEAIKR-AGIKAEQIDEVIFGCVLQAGL 62
           +V +    RTP+G +GG L  V +  LGA+ +   + R  G+  E +D+VIFGC  QAG 
Sbjct: 3   QVFICDYIRTPIGRYGGALSPVRADDLGAVPLKALMARNGGVDWEAVDDVIFGCANQAGE 62

Query: 63  -GQNVARQCMINAGIPKEVTAFTINKVCGSGLRAVSLAAQVIKAGDADIIMAGGTENMDK 121
             +NVAR   + AG+P  VT  TIN++CGSG+ AV  AA+ I AG+AD+++AGG E+M +
Sbjct: 63  DNRNVARMSALLAGLPVGVTGTTINRLCGSGMDAVLTAARQIAAGEADLVIAGGVESMSR 122

Query: 122 APFILPNARWGYRMSMPKGDLID--EMVWGGLTDVFNGYHMGITAENINDMYGITREEQD 179
           APF+LP A   +  S    D       V   +   +    M  T +N+   +GI+RE QD
Sbjct: 123 APFVLPKAGTAFTRSAEIHDTTIGWRFVNPAMEAAYGVDPMPQTGQNVACDFGISREAQD 182

Query: 180 AFGFRSQTLAAQAIESGRFKDEIVPVVIKGKKGDIV-FDTDEHPRKSTPEAMAKLAPAFK 238
           A    SQT AA A  +GR   EI PV++  ++G+ V  + DEHPR +TPEA+AKL P F 
Sbjct: 183 AMALASQTKAAAAQANGRLAQEITPVLVPQRRGEPVRVEQDEHPRATTPEALAKLKPLFA 242

Query: 239 KGGSVTAGNASGINDAAAAVIVMSKEKADELGIKPMAKVVSYASGGVDPSVMGLGPIPAS 298
            GGSVTAGN+SG+ND AAA+I+ S+      G+ P+A+V+  A+ GV P +MG+GP+PA+
Sbjct: 243 -GGSVTAGNSSGVNDGAAALILASEAAVRRHGLTPIARVLGGATAGVPPRIMGIGPVPAA 301

Query: 299 RKALEKAGLTIDDIDLIEANEAFAAQSIAVARDLGWADKMEKVNVNGGAIAIGHPIGSSG 358
            K + + GLT +  D+IE NEAFAAQ +A  R LG A++  +VN NGGAIA+GHP+G SG
Sbjct: 302 LKLMARLGLTTEAFDVIELNEAFAAQGVATLRQLGIAEEDARVNPNGGAIALGHPLGMSG 361

Query: 359 ARILVTLLYEMQKRGSKKGLATLCIGGGMGTALIVE 394
           ARI  T   ++Q+ G ++ L+ +CIG G G A+ +E
Sbjct: 362 ARITGTAALQLQRTGGRRALSAMCIGVGQGIAIALE 397


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: 485
Number of extensions: 25
Number of successful extensions: 6
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: 399
Length adjustment: 31
Effective length of query: 365
Effective length of database: 368
Effective search space:   134320
Effective search space used:   134320
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 10 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