GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtD in Desulfovibrio vulgaris Miyazaki F

Align CbtD, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate 8501090 DvMF_1826 oligopeptide/dipeptide ABC transporter, ATPase subunit (RefSeq)

Query= TCDB::Q97VF5
         (362 letters)



>FitnessBrowser__Miya:8501090
          Length = 333

 Score =  179 bits (454), Expect = 9e-50
 Identities = 108/329 (32%), Positives = 175/329 (53%), Gaps = 18/329 (5%)

Query: 45  ILEVHNLNVIYDEGNSRIIKAVNDVSFGVEKGEILGIIGESGSGKTTLISAILRAIRPPG 104
           +L+V NL V +   ++ +  AVNDVSF + KGE LG++GESG+GK+    +IL  +  PG
Sbjct: 4   LLDVSNLTVKFALRDTALT-AVNDVSFTLAKGERLGLVGESGAGKSVTGFSILNLVSKPG 62

Query: 105 KIISGKVIFNGMDIFSMTIDEFRKLLWKDISYVPQASQNALNPVLPISEIFYHEAISHGE 164
            I  G V+F G D+     +  R +    IS + Q     LNPVL +        ++H +
Sbjct: 63  FIAGGSVLFEGKDLTRADAETLRDIRGNRISMIFQDPMMTLNPVLTVGTQMIETILAHKK 122

Query: 165 ADKKRVIERASELLKLVGL-DPARVLKMYPFQLSGGMKQRVMIALSLLLNPKLILMDEPT 223
             +K     A + L+ V +  P R L  YP + SGGM+QR++IA++LL +P LI+ DEPT
Sbjct: 123 VTRKEAEAIALDKLRKVYIPSPERRLAQYPHEFSGGMRQRIVIAIALLTSPSLIIADEPT 182

Query: 224 SALDMLNQELLLKLIKNINQEMGVTIVYVTHDILNIAQIANRLLVMYKGYVMEEGKTEEI 283
           +ALD+  Q  ++ L+  + Q   + ++ +THD+  ++Q+  ++ VMY G ++E G T  +
Sbjct: 183 TALDVTIQAEIMDLLLELCQSEDMGLILITHDLGVVSQVTQKIAVMYAGGIVEMGDTAMV 242

Query: 284 IKSPLNPYTSLLVSSIPSLKGEV--------------KVINVPLDEPLVSK-EKGCPFLA 328
           +  PL+PYT  L+ ++P    +               ++  +P   P +S   +GCPF  
Sbjct: 243 VGEPLHPYTRGLLGALPQCADKADCGLEDVAAPRVRRRLNQIPGSMPSLSDVPRGCPFNN 302

Query: 329 RCSKAFGRCKEELPEIRLVYD-RKVRCHL 356
           RC      C    P + +  D R   CH+
Sbjct: 303 RCELCETVCTTTRPLLEVKSDGRMAACHM 331


Lambda     K      H
   0.319    0.138    0.391 

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: 237
Number of extensions: 11
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: 362
Length of database: 333
Length adjustment: 29
Effective length of query: 333
Effective length of database: 304
Effective search space:   101232
Effective search space used:   101232
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: 49 (23.5 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