GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Novosphingobium fuchskuhlense FNE08-7

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 (characterized)
to candidate WP_067911530.1 AQZ52_RS13185 acetyl-CoA C-acetyltransferase

Query= SwissProt::P14611
         (393 letters)



>NCBI__GCF_001519075.1:WP_067911530.1
          Length = 410

 Score =  313 bits (802), Expect = 6e-90
 Identities = 188/408 (46%), Positives = 252/408 (61%), Gaps = 19/408 (4%)

Query: 1   MTDVVIVSAARTAVGKFGGSLAKIPAPELGAVVIKAALERAGVKPEQVSEVIMGQVLTAG 60
           +T   IV+  RTAVGKFGGSLA + A +LGAV++KA +ER  + P +V +V+  Q    G
Sbjct: 4   LTRAAIVAPIRTAVGKFGGSLADLNAGQLGAVILKALMERTKIDPARVDDVVFSQGY--G 61

Query: 61  SGQNPA--RQAAIKAGLPAMVPAMTINKVCGSGLKAVMLAANAIMAGDAEIVVAGGQENM 118
           + + PA    + + AGLP  VP   +++ CGSGL+AV+ AA  +  G +++VVAGG E+M
Sbjct: 62  NAEAPAIGHWSWLAAGLPLEVPGYQLDRRCGSGLQAVINAAMMVQTGQSDVVVAGGVESM 121

Query: 119 SAAPHVLPGSRDGFRMGDAKLVDTMIVDGLWDVYNQYHMGI------TAENVAKEYGITR 172
           S   +     R G R G   L D +    L     +   G+      TAEN+A++Y I+R
Sbjct: 122 SNVEYYTTEGRRGTRAGGLMLHDRLTRGRLMSQPIE-RFGVISGMIETAENLARDYHISR 180

Query: 173 EAQDEFAVGSQNKAEAAQKAGKFDEEIVPVLIPQRKGDPVAFKTDEFVRQGATLDSMSGL 232
           EA D +AV S  +A AA K G FD+E+VPV IPQ+KGDP  F  DE  R  AT++S+  L
Sbjct: 181 EACDAYAVRSHQRAAAAWKNGLFDDELVPVEIPQKKGDPKIFAHDEGYRADATMESLGAL 240

Query: 233 KPAFDKA---GTVTAANASGLNDGAAAVVVMSAAKAKELGLTPLATIKSYANAGVDPKVM 289
           K    KA     VTA NAS  ND AAA +V++  K +ELGL P+A   S+A AG DP  M
Sbjct: 241 KALEAKAIPGAVVTAGNASQQNDAAAACLVVAEHKLEELGLEPIAWFHSWAAAGCDPARM 300

Query: 290 GMGPVPASKRALSRAEWTPQDLDLMEINEAFAAQALAVHQQMGW--DTSK---VNVNGGA 344
           G+GPVPA +R  +R      D+DL+E+NEAFA Q LAV +  GW  D S+   +NVNG  
Sbjct: 301 GIGPVPAVERLFARTGLGWNDIDLVELNEAFAPQVLAVLKGWGWSDDDSRHDMLNVNGSG 360

Query: 345 IAIGHPIGASGCRILVTLLHEMKRRDAKKGLASLCIGGGMGVALAVER 392
           I++GHPIGA+G RIL  L  E+ RRD + GL ++CIGGG G+A   ER
Sbjct: 361 ISLGHPIGATGGRILANLTRELVRRDGRFGLETMCIGGGQGIAAVFER 408


Lambda     K      H
   0.315    0.131    0.369 

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: 398
Number of extensions: 17
Number of successful extensions: 5
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: 410
Length adjustment: 31
Effective length of query: 362
Effective length of database: 379
Effective search space:   137198
Effective search space used:   137198
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