GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Desulfatiglans anilini DSM 4660

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate WP_244155446.1 H567_RS0109105 oligopeptide/dipeptide ABC transporter ATP-binding protein

Query= TCDB::Q97VF4
         (324 letters)



>NCBI__GCF_000422285.1:WP_244155446.1
          Length = 337

 Score =  199 bits (506), Expect = 8e-56
 Identities = 116/324 (35%), Positives = 186/324 (57%), Gaps = 18/324 (5%)

Query: 4   MELKGVSVIFEDKVGLFKKRK--FYALKDVSLSMNQGDLLIVLGESGAGKTTLGRVIVGL 61
           M+L+ V  ++E K  LF + +    AL  + L ++ G++  ++GESG+GKTT GR+I+ L
Sbjct: 1   MKLEKVRKVYETKGNLFGRGRGQVVALDHLDLDIHHGEIFGLVGESGSGKTTAGRLILRL 60

Query: 62  QKPTSGEVVYDGYNIWKNKRKIFKKYRKDVQLIPQDPYSTLPFNKTVEEILVAPILRWEK 121
           ++P  G ++ DG +    K K  K +RK VQ+I QDPY +L    ++ + +  P+L    
Sbjct: 61  EEPDGGRILLDGQDTCTLKGKALKAFRKRVQMIFQDPYQSLNPQISILDAVSEPLLIHTA 120

Query: 122 INKDELRKRLINLLELVKLTPAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIVADEPV 181
             + +  +   ++L  V L+P E+FL ++PHQLSGGQ+QR++IAR++ + P ++VADEP 
Sbjct: 121 SKRTDRLEAARDILGRVGLSPPEDFLFRFPHQLSGGQRQRVAIARAMILGPDVVVADEPT 180

Query: 182 TMVDASLRIGILNTLAEIKNRLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGRIVERA 241
           +M+DAS+   I N L E++  +N+T++FITH +  ARY  +        V++ G +VE  
Sbjct: 181 SMLDASISAQIFNILLELREAMNVTLLFITHSLAAARYLCN-----RIAVLYRGHLVELG 235

Query: 242 DLEEILKDPLHPYTNDLIKLTPSIDNLYKEINVKINYERVE-------KGCPYRLRCPFA 294
             +EI+  P HPYT  LI   P   +   ++       RV+        GCP+  RC  A
Sbjct: 236 PADEIIYRPAHPYTQALIDAIPKFGDC-SDLKRYGTLLRVDSEGAGSVSGCPFLPRCAVA 294

Query: 295 MDIC---KNEEPKLFKYSHEVACF 315
             +    KN E +LF   H VAC+
Sbjct: 295 QRLYCSQKNPEIRLFAPDHWVACY 318


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: 300
Number of extensions: 19
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: 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 Apr 09 2024. 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