GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Cupriavidus basilensis 4G11

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate RR42_RS35215 RR42_RS35215 peptide ABC transporter ATP-binding protein

Query= TCDB::Q97VF4
         (324 letters)



>FitnessBrowser__Cup4G11:RR42_RS35215
          Length = 329

 Score =  177 bits (450), Expect = 2e-49
 Identities = 111/332 (33%), Positives = 181/332 (54%), Gaps = 20/332 (6%)

Query: 3   LMELKGVSVIFEDKVGLFKKRKFYALK---DVSLSMNQGDLLIVLGESGAGKTTLGRVIV 59
           ++ ++ + V F    G+F KR+  ++K    VS ++ +G+ L ++GESG GK+T G  I+
Sbjct: 5   ILRVENLKVHFPVTQGVFIKRQVGSVKAVDGVSFTLRRGETLGLVGESGCGKSTTGLAII 64

Query: 60  GLQKPTSGEVVYDGYNIWKNKRKIFKKYRKDVQLIPQDPYSTLPFNKTVEEILVAPILRW 119
            +   + G + +DG +     +   K +R+ VQ++ QDP+ +L     V +I+  P+   
Sbjct: 65  KMLAASGGRIAFDGDDFATFSKAQEKNFRRSVQMVYQDPFGSLNPRMKVCDIIGEPLEVH 124

Query: 120 EKIN-KDELRKRLINLLELVKLTPAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIVAD 178
              N ++  R R+  LL++V L P      +YPH+ SGGQ+QR+ IAR+L+V P +IV D
Sbjct: 125 GMANDREHYRARIAELLQMVGLLPY--MADRYPHEFSGGQRQRIGIARALAVEPSLIVCD 182

Query: 179 EPVTMVDASLRIGILNTLAEIKNRLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGRIV 238
           EPV+ +D S++  ++N   E++ RL LT +FI HD+ + R   H+ D+    VM+ GRIV
Sbjct: 183 EPVSALDVSIQAQVVNVFMELQRRLGLTYIFIAHDLAVVR---HISDR--IAVMYLGRIV 237

Query: 239 ERADLEEILKDPLHPYTNDLIKLTP--SIDNLYKEINVKINYE-----RVEKGCPYRLRC 291
           E A  + +  +P HPYT  L+   P  S++   K   + +  E         GC +  RC
Sbjct: 238 EIASRDALYANPRHPYTKALLSAVPVASVEAEAKRQRIVLKGEVPSPLNPPSGCRFHPRC 297

Query: 292 PFAMDICKNEEPKLFKY--SHEVACFLYGKVG 321
             A   C+ E+P L +      VAC L G  G
Sbjct: 298 AQATQRCRVEDPVLRERGDGQMVACHLEGLEG 329


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: 282
Number of extensions: 13
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: 329
Length adjustment: 28
Effective length of query: 296
Effective length of database: 301
Effective search space:    89096
Effective search space used:    89096
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:

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