GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Brucella microti CCM 4915

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 (characterized)
to candidate WP_004689226.1 BMI_RS08205 acetyl-CoA C-acetyltransferase

Query= SwissProt::P50174
         (393 letters)



>NCBI__GCF_000022745.1:WP_004689226.1
          Length = 394

 Score =  635 bits (1638), Expect = 0.0
 Identities = 319/393 (81%), Positives = 355/393 (90%), Gaps = 1/393 (0%)

Query: 1   MSNP-SIVIASAARTAVGSFNGAFGNTLAHELGAAAIKAVLERAGVEAGEVDEVILGQVL 59
           MS+P SIVIASAARTAVG+FNGAF N  AHELGA AIKA LERAGV+A +VDEVILGQVL
Sbjct: 1   MSDPKSIVIASAARTAVGAFNGAFANVPAHELGAVAIKAALERAGVDAADVDEVILGQVL 60

Query: 60  PAGEGQNPARQAAMKAGLPQEKTAWGMNQLCGSGLRAVALGMQQIATGDAKVIVAGGMES 119
            AGEGQNPARQAAM AG P+E TA+ +NQLCGSGLRAVALGMQQI +GDAK+IVAGG ES
Sbjct: 61  TAGEGQNPARQAAMGAGCPKETTAFAINQLCGSGLRAVALGMQQIVSGDAKIIVAGGQES 120

Query: 120 MSMAPHCAHLRGGVKMGDYKMIDTMIKDGLTDAFYGYHMGITAENVARKWQLTREEQDEF 179
           MSMAPHCA+LR GVKMGD+KMIDTM+KDGLTDAF+GYHMGITAEN+AR+WQL+R EQDEF
Sbjct: 121 MSMAPHCAYLRSGVKMGDFKMIDTMLKDGLTDAFHGYHMGITAENIARQWQLSRSEQDEF 180

Query: 180 ALASQNKAEAAQKAGRFADEIVPFVVKTRKGDVNVDQDEYIRHGATLDSIAKLRPAFDKE 239
           ALASQ+KAEAAQKAGRF +EIVPF VK RKGDV V  DEYIR G T++ +AKL+PAFDKE
Sbjct: 181 ALASQHKAEAAQKAGRFDEEIVPFTVKARKGDVVVSADEYIRPGTTMEVLAKLKPAFDKE 240

Query: 240 GTVTAGNASGLNDGAAAALLMTEAEAARRGIQPLARIVSWATAGVDPQIMGTGPIPASRK 299
           GTVTAGNASG+NDGAAA +LM   EAARRG++PLARIVSWATAGVDP IMGTGPIPA+RK
Sbjct: 241 GTVTAGNASGINDGAAAVVLMDAGEAARRGVKPLARIVSWATAGVDPSIMGTGPIPATRK 300

Query: 300 ALEKAGWSVADIELVEANEAFAAQACAVNKDLGWDPSIVNVNGGAIAIGHPIGASGARVL 359
           ALEKAGWSV D++LVEANEAFAAQ+CAV +DLG +P IVNVNGGAIAIGHPIGASGARVL
Sbjct: 301 ALEKAGWSVGDLDLVEANEAFAAQSCAVVRDLGLNPEIVNVNGGAIAIGHPIGASGARVL 360

Query: 360 NTLLFEMKRRGVSKGLATLCIGGGMGVAMCVER 392
            TLL+EM+RR   +GLATLCIGGGMGVA+CVER
Sbjct: 361 TTLLYEMERRDAKRGLATLCIGGGMGVALCVER 393


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: 561
Number of extensions: 18
Number of successful extensions: 2
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: 394
Length adjustment: 31
Effective length of query: 362
Effective length of database: 363
Effective search space:   131406
Effective search space used:   131406
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