GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Klebsiella michiganensis M5al

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate BWI76_RS26865 BWI76_RS26865 dipeptide ABC transporter ATP-binding protein

Query= TCDB::Q97VF4
         (324 letters)



>FitnessBrowser__Koxy:BWI76_RS26865
          Length = 337

 Score =  191 bits (485), Expect = 2e-53
 Identities = 108/307 (35%), Positives = 179/307 (58%), Gaps = 14/307 (4%)

Query: 16  KVGLFK-KRKFYALKDVSLSMNQGDLLIVLGESGAGKTTLGRVIVGLQKPTSGEVVYDGY 74
           K GLF  +R   AL  VS ++ +G  L V+GESG GK+TLGR++  ++ PT GE+ Y G 
Sbjct: 25  KKGLFAPERLVKALDGVSFTLERGKTLAVVGESGCGKSTLGRLLTMIEIPTGGELYYQGQ 84

Query: 75  NIWKNKRKIFKKYRKDVQLIPQDPYSTLPFNKTVEEILVAPILRWEKINKDELRKRLINL 134
           ++ K+  +  K  R+ +Q++ Q+PY +L   K V +IL  P+     ++K++ R++ + +
Sbjct: 85  DLLKHDPQAQKLRRQKIQIVFQNPYGSLNPRKKVGQILEEPLQINTSLSKEQRREKALAM 144

Query: 135 LELVKLTPAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIVADEPVTMVDASLRIGILN 194
           +  V L    E   +YPH  SGGQ+QR++IAR L ++P +++ADEPV+ +D S+R  +LN
Sbjct: 145 MAKVGLKT--EHYDRYPHMFSGGQRQRIAIARGLMLDPDVVIADEPVSALDVSVRAQVLN 202

Query: 195 TLAEIKNRLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGRIVERADLEEILKDPLHPY 254
            + +++  L L+ VFI+HD+ +     H+ D+   +VM+ GR VE+   ++I  +P HPY
Sbjct: 203 LMMDLQQDLGLSYVFISHDLSVVE---HIADE--VMVMYLGRCVEKGSKDQIFNNPQHPY 257

Query: 255 TNDLIKLTPSIDNLYKEINVKINYE-----RVEKGCPYRLRCPFAMDICKNEEPKLFKYS 309
           T  L+  TP ++   +   +K+  E         GC +  RC      C   +P+L  Y 
Sbjct: 258 TQALLSATPRLNPDDRRERIKLTGELPSPLNPPPGCAFNARCRRRFGPCTQLQPQLKDYG 317

Query: 310 HE-VACF 315
            + VACF
Sbjct: 318 GQLVACF 324


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: 320
Number of extensions: 16
Number of successful extensions: 4
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: 337
Length adjustment: 28
Effective length of query: 296
Effective length of database: 309
Effective search space:    91464
Effective search space used:    91464
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