GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Desulfovibrio vulgaris Miyazaki F

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate 8501378 DvMF_2110 oligopeptide/dipeptide ABC transporter, ATPase subunit (RefSeq)

Query= TCDB::Q97VF4
         (324 letters)



>FitnessBrowser__Miya:8501378
          Length = 316

 Score =  158 bits (399), Expect = 2e-43
 Identities = 98/305 (32%), Positives = 165/305 (54%), Gaps = 44/305 (14%)

Query: 27  ALKDVSLSMNQGDLLIVLGESGAGKTTLGRVIVGLQKPTSGEVVYDGYNIWKNKRKIFKK 86
           A+  VSL++++G  L ++GESG GK+TL R++VGL  P++G+V+ DG        ++F  
Sbjct: 11  AVDGVSLTLDRGRTLGLVGESGCGKSTLARMVVGLLPPSAGQVLLDG--------RLFAG 62

Query: 87  YRKD-----------------------VQLIPQDPYSTLPFNKTVEEILVAPILRWEKIN 123
              D                       VQ++ QDP+S+L   +TV    +   L    + 
Sbjct: 63  TDGDAANGGASGHSADLAISRAEAAQLVQMVFQDPFSSLNPRRTVGAS-IGEALAVAGVP 121

Query: 124 KDELRKRLINLLELVKLTPAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIVADEPVTM 183
             E R ++ ++L+LV L    E   +YPH+ SGGQ+QR+++AR+L  +P ++V DEPV+ 
Sbjct: 122 GPERRAKVADMLQLVGLRA--EHADRYPHEFSGGQRQRVAVARALITHPALVVCDEPVSS 179

Query: 184 VDASLRIGILNTLAEIKNRLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGRIVERADL 243
           +DAS++  +LN L E++  + L  +FI+HD+ +     H+ D  +  VM+ G++VE A  
Sbjct: 180 LDASVQAQVLNLLRELQEHMGLAYLFISHDLGVVG---HMSD--HVAVMYLGKVVEEAPR 234

Query: 244 EEILKDPLHPYTNDLIKLTPSIDNLYKEINVKINYE-----RVEKGCPYRLRCPFAMDIC 298
           + +   P HPYT  L+   P  D   +  +  ++ +         GCP+  RCP  MD+C
Sbjct: 235 DVLFAAPAHPYTRALLASVPVRDPSRRAEHPALSGDLPSPIAPPPGCPFHPRCPQVMDVC 294

Query: 299 KNEEP 303
           + + P
Sbjct: 295 RRQVP 299


Lambda     K      H
   0.321    0.141    0.410 

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: 264
Number of extensions: 11
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: 324
Length of database: 316
Length adjustment: 28
Effective length of query: 296
Effective length of database: 288
Effective search space:    85248
Effective search space used:    85248
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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