GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Derxia gummosa DSM 723

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 (characterized)
to candidate WP_028311694.1 H566_RS0112420 acetyl-CoA acetyltransferase

Query= SwissProt::P50174
         (393 letters)



>NCBI__GCF_000482785.1:WP_028311694.1
          Length = 398

 Score =  293 bits (749), Expect = 8e-84
 Identities = 169/397 (42%), Positives = 241/397 (60%), Gaps = 19/397 (4%)

Query: 8   IASAARTAVGSFNGAFGNTLAHELGAAAIKAVLERA-GVEAGEVDEVILGQVLPAGE-GQ 65
           + +A RT V   NGAF +    +L A A++ ++ RA G++  E+ +VI+G  +P  E G 
Sbjct: 10  LVAAVRTPVARRNGAFRHARPDDLLAHALRELVARAPGLDPAEIADVIVGCAMPEAEQGM 69

Query: 66  NPARQAAMKAGLPQEKTAWGMNQLCGSGLRAVALGMQQIATGDAKVIVAGGMESMSMAPH 125
           N AR   + AGLP     + +N+ C SGL+AVA    +I +G+A+V++A G+ESM++   
Sbjct: 70  NVARIGLLLAGLPASVPGFTVNRFCASGLQAVADAAARIRSGEAEVMIAAGVESMTVMTK 129

Query: 126 CAHLRGGVKMGDYKMIDTMIKDGLTDAFYGYHMGITAENVARKWQLTREEQDEFALASQN 185
                    MG+    +    +        + MG+TAE VAR+W ++R EQD FA+ S  
Sbjct: 130 M--------MGNRVRPNPAFFEHDEHRAIAWGMGLTAEEVARRWNVSRAEQDAFAVESHK 181

Query: 186 KAEAAQKAGRFADEIVPFVVKTRKGDVN---------VDQDEYIRHGATLDSIAKLRPAF 236
           +A AA  AGRFADEI P++  + +   +         V  DE  R  A+ + I  LRP F
Sbjct: 182 RAIAAIDAGRFADEIAPYITTSARPGSDGQPLRTTSVVTHDEGPRRDASPERIGALRPVF 241

Query: 237 DKEGTVTAGNASGLNDGAAAALLMTEAEAARRGIQPLARIVSWATAGVDPQIMGTGPIPA 296
             +G+VTAGNAS ++DGAAA LLM+E    R G+QP+AR V+ A AGV P++MG GP+ A
Sbjct: 242 AADGSVTAGNASQMSDGAAAVLLMSEVALKRSGLQPIARFVAHAVAGVPPEVMGIGPVEA 301

Query: 297 SRKALEKAGWSVADIELVEANEAFAAQACAVNKDLGWDPSIVNVNGGAIAIGHPIGASGA 356
             +AL +AGW    ++ +E NEAFAAQA AV + LG DP+ +N  GGAIA+GHP+GA+GA
Sbjct: 302 IPRALARAGWRQDSLDWIELNEAFAAQAIAVRRTLGLDPAQINPLGGAIALGHPLGATGA 361

Query: 357 RVLNTLLFEMKRRGVSKGLATLCIGGGMGVAMCVERL 393
               TLL  MKR    +G+ T+CIG GMG A  +ER+
Sbjct: 362 IRTATLLAAMKRGDARRGMVTMCIGTGMGAAGVIERV 398


Lambda     K      H
   0.317    0.132    0.381 

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: 393
Number of extensions: 22
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: 398
Length adjustment: 31
Effective length of query: 362
Effective length of database: 367
Effective search space:   132854
Effective search space used:   132854
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