GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Beijerinckia mobilis UQM 1969

Align Acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate WP_034994514.1 DL88_RS08065 acetyl-CoA C-acyltransferase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2411
         (393 letters)



>NCBI__GCF_000745425.1:WP_034994514.1
          Length = 373

 Score =  272 bits (695), Expect = 1e-77
 Identities = 165/394 (41%), Positives = 223/394 (56%), Gaps = 32/394 (8%)

Query: 5   EIYVVSAARTAIGTFG-GSLKDVPLADLATTAVKAALERAAVDPALVGHLVMGNVIPTET 63
           E Y+V   RT       G+L  +   DLA + + A   R       +  + +G   P   
Sbjct: 3   EAYIVDYLRTPFAPANRGALAGIRPDDLAASVIAALAARMDFAIEEIEDVNLGCAFPEGE 62

Query: 64  RDAYISRVAAMNAGIPKETPAYNVNRLCGSGLQAIINAAQTLMLGDADIVVGAGAESMSR 123
           +   I+R AA+ AG+P+      VNR CGS +QAI  AA  + +G  +  +  G ESMSR
Sbjct: 63  QGLNIARCAALTAGLPQSIGGVTVNRWCGSSMQAIQMAAGAISMGAGEAFIAGGVESMSR 122

Query: 124 GPYL----MPAARW--GSRMGNAQVIDYMLGILHDPFHGIHMGITAENVAARNGITREMQ 177
            P +    +P   W  G R+                   ++MG+TAEN+A R GI+RE Q
Sbjct: 123 VPMMGFNPLPNPSWPEGRRLTF-----------------VNMGLTAENLAERYGISREEQ 165

Query: 178 DALAFEDQQRAAHAIANGYFSEQIATVEIQDRKGVKLFSVDEHPRATSLEQLAAMKPAFK 237
           D  +   Q+++  A A+G  + +IA V      G         PR T   +LA +K  FK
Sbjct: 166 DDYSLASQKKSLAARADGRLAAEIAPVGAIVEDGC--------PRETDTTKLAGLKTVFK 217

Query: 238 KDGSVTAGNASGLNDGAAALVMASGNAVQANNLKPLARLVSYAHAGVEPEFMGLGPIPAT 297
            +GSVTAGN+S L DGA+A ++ S + ++   LKPLAR+VS+A +G EPE MG+GP+ A+
Sbjct: 218 AEGSVTAGNSSPLTDGASATLVCSEDFIKRRGLKPLARVVSFAISGCEPEIMGIGPVEAS 277

Query: 298 RLALKRAGLTVADLDVIEANIAFAAQACAVSQELDLDPAKVNPNGSGIALGHPVGATGAI 357
           R ALKRAG+T  DLDVIE N AFA Q  A  +ELD+DPA++N +G  IALGHP+GATGA 
Sbjct: 278 RKALKRAGITATDLDVIEMNEAFAVQVLACCRELDIDPARLNRDGGAIALGHPLGATGAR 337

Query: 358 IATKAIHELHRTGGRYALVTMCIGGGQGIAAIFE 391
           +A KA   L R  GRY L T CIGGGQGIA + E
Sbjct: 338 LAGKAASLLKRDQGRYGLATQCIGGGQGIALVLE 371


Lambda     K      H
   0.318    0.133    0.378 

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: 372
Number of extensions: 21
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: 373
Length adjustment: 30
Effective length of query: 363
Effective length of database: 343
Effective search space:   124509
Effective search space used:   124509
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