GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dgoK in Caulobacter crescentus NA1000

Align Probable 2-dehydro-3-deoxygalactonokinase DgoK1; 2-keto-3-deoxy-galactonokinase; 2-oxo-3-deoxygalactonate kinase; EC 2.7.1.58 (characterized)
to candidate CCNA_00826 CCNA_00826 2-dehydro-3-deoxygalactonokinase

Query= SwissProt::Q92RN7
         (306 letters)



>FitnessBrowser__Caulo:CCNA_00826
          Length = 306

 Score =  181 bits (458), Expect = 2e-50
 Identities = 122/299 (40%), Positives = 157/299 (52%), Gaps = 16/299 (5%)

Query: 11  DWGTSSFRLWIIGEDGAVLAERRSAEGMTTAAKTGFHTILD--GHLAAVSAPAHLPIIIC 68
           DWG S  RLW+    G  +  RR   G+T    +   T LD  G     + P +   I+C
Sbjct: 10  DWGGSRLRLWL--RQGKSVIHRRDGPGVTALTDSPEKTFLDLVGDWRE-AGPDYA--ILC 64

Query: 69  GMAGARQGWKEAGYIETPAALAEIAGRATAIPDVDRDIRILPGLA-QRDRRHPDVMRGEE 127
           GM G+R GW EA Y   PA   +IA RA  I      +RI+PGL+       PDVMRGEE
Sbjct: 65  GMVGSRMGWTEAPYAPCPATTGQIAARAVRIEAAGLPVRIVPGLSCVNPLGGPDVMRGEE 124

Query: 128 TQLLGAA---AHLGAGSHLVCMPGTHSKWVRLADDRVEGFSTFMTGELFDTIARHTILSH 184
           TQ+LGA    A L +G HL+ +PGTH+KW  + D ++  F T   GE F  +  H+ L  
Sbjct: 125 TQILGALSLDAALRSGRHLLVLPGTHNKWAVVEDGQITTFLTAPIGETFALLKAHSTLG- 183

Query: 185 AVAEADTFAAGSAA-FTDAVSRTRENPA-LATNLLFSVRAGQLLHGTAAADARAQLSGTL 242
             A   + A GSAA F   ++R  E  A   T+L+F  RA QLL     ADA   LSG L
Sbjct: 184 --AGGGSLAEGSAAGFARGLTRIAEQGAGRLTHLMFETRARQLLEAMTPADAMGFLSGLL 241

Query: 243 IGLEIAGALAGSGSVDGVCLVGSGGLGTLYRTALESQGLNVRAVDADEAVRAGLSAAAR 301
           IG ++A A    G ++ V ++G G L  LY  AL + G+   AVD D AV AGLS   R
Sbjct: 242 IGADVAAARDWFGPMEAVTVIGDGPLAALYVQALAATGVTASAVDGDAAVLAGLSMITR 300


Lambda     K      H
   0.319    0.133    0.394 

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: 260
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: 306
Length of database: 306
Length adjustment: 27
Effective length of query: 279
Effective length of database: 279
Effective search space:    77841
Effective search space used:    77841
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 48 (23.1 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