GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Geobacter daltonii FRC-32

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate WP_012648527.1 GEOB_RS17190 dipeptide ABC transporter ATP-binding protein

Query= TCDB::Q97VF4
         (324 letters)



>NCBI__GCF_000022265.1:WP_012648527.1
          Length = 324

 Score =  193 bits (490), Expect = 5e-54
 Identities = 114/326 (34%), Positives = 183/326 (56%), Gaps = 15/326 (4%)

Query: 3   LMELKGVSVIFEDKVGLFKKRKFY-ALKDVSLSMNQGDLLIVLGESGAGKTTLGRVIVGL 61
           L+E K ++  F  K G F +++   A+  + L + +G+ L V GESG GK+T+ ++++GL
Sbjct: 4   LIEAKSLAKHFPVKAGQFGRQQLLKAVDGIDLHIGKGETLGVAGESGCGKSTVAKLLMGL 63

Query: 62  QKPTSGEVVYDGYNIWKNKRKIFKKYRKDVQLIPQDPYSTLPFNKTVEEILVAPILRWEK 121
            KP+ G + Y G ++    +     +RK VQ+I QDP+S+L     V +I+  P      
Sbjct: 64  IKPSGGSITYQGKSLVDMGKVERASFRKTVQMIFQDPFSSLNPRMRVGDIIGEPFTVHGL 123

Query: 122 INKDELRKRLINLLELVKLTPAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIVADEPV 181
            +    R  +I L+  V L+  EE   +YPH+ SGGQ+QR+ IAR+L+V+P++++ADEPV
Sbjct: 124 ASGARKRDLVIGLMAKVGLS--EEHFYRYPHEFSGGQRQRIGIARALAVSPKLLIADEPV 181

Query: 182 TMVDASLRIGILNTLAEIKNRLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGRIVERA 241
           + +D S++  I+N L E+K    L+ +FITHD+ + R   HL D+    +M+ G++VE  
Sbjct: 182 SALDISIQAQIINLLMELKREYGLSFLFITHDLSVIR---HLSDR--IAIMYLGKVVESG 236

Query: 242 DLEEILKDPLHPYTNDLIKLTPSIDNLYKEINVKINYE-----RVEKGCPYRLRCPFAMD 296
             +E+L   LHPYT  L+   P ID       + +  +         GCP+  RCP+A +
Sbjct: 237 TRDEVLDRYLHPYTQALLSAVPRIDPDRTTGRIVLQGDLPSPIHPPSGCPFHTRCPYAEN 296

Query: 297 ICKNEEPKLFKY--SHEVACFLYGKV 320
           IC  E P L +    H  AC    K+
Sbjct: 297 ICSKEPPPLEEKEPEHLAACHFSQKL 322


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: 336
Number of extensions: 20
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: 324
Length adjustment: 28
Effective length of query: 296
Effective length of database: 296
Effective search space:    87616
Effective search space used:    87616
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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