GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Dyella japonica UNC79MFTsu3.2

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate N515DRAFT_0938 N515DRAFT_0938 acetyl-CoA C-acetyltransferase

Query= metacyc::MONOMER-20679
         (395 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0938
          Length = 394

 Score =  202 bits (514), Expect = 1e-56
 Identities = 141/406 (34%), Positives = 205/406 (50%), Gaps = 35/406 (8%)

Query: 5   VIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRAGIDPKEVEDVVMGAAMQQGATG 64
           VI    RT IG ++ G         L   AI+ A+++AGI  ++V +V+MG  +     G
Sbjct: 7   VIAGAKRTAIG-SFLGQFTGVPTPVLGATAIKAALEQAGIAAQDVNEVLMGCVLPANL-G 64

Query: 65  GNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESISLVQ 124
              AR+A L+AGLP     TT+++ C SG++AI L    +      + V GG ES++   
Sbjct: 65  QAPARQAALKAGLPAAVGCTTVNKVCGSGMKAIMLGHDLIKAGSAAVVVAGGMESMT--- 121

Query: 125 NDKMNTFHAVDPALEAIKGDVYM----------------AMLDTAETVAKRYGISRERQD 168
               N  H V+       GD  +                AM    E  A +Y  +RE QD
Sbjct: 122 ----NAPHMVNARTGIRYGDGQLVDHMAWDGLTNPYDGKAMGVFGELCADKYHFTREEQD 177

Query: 169 EYSLESQRRTAAAQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETTAE 228
            +++ES +R  AAQQ G F  EI P+          T A    D+ +  DE P     A+
Sbjct: 178 AFAIESVKRAQAAQQNGAFAGEIVPV----------TVAGRKGDVVVDTDEQPGRSDIAK 227

Query: 229 GLAGLKAVRGEGFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCEPD 288
             +   A R E  TITA ++S +SDGA+A V++S   A A+GL+PL       ++  EP+
Sbjct: 228 VPSLKPAFRKENGTITAASSSSISDGAAAVVLLSADDAKARGLQPLARIVAHATHSQEPE 287

Query: 289 EMGIGPVFAVPRLLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGIDPEKLNVNGGAISV 348
                PV A+ ++L + G  VDD+ L+E+NEAFAV  +    +LGI   KLNVNGGA ++
Sbjct: 288 WFTTAPVSAIQKVLDKAGWKVDDVDLFEVNEAFAVVAMAPMRELGIPHAKLNVNGGACAL 347

Query: 349 GHPYGMSGARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFEIV 394
           GHP G SG RL    L   + R  K  V ++C+GGG  +A   E++
Sbjct: 348 GHPIGASGTRLVVTLLNALQTRGLKRGVASLCIGGGEATAIAVELL 393


Lambda     K      H
   0.316    0.134    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: 394
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: 395
Length of database: 394
Length adjustment: 31
Effective length of query: 364
Effective length of database: 363
Effective search space:   132132
Effective search space used:   132132
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 17 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