GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Hippea alviniae EP5-r

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate WP_022670625.1 G415_RS0105555 ABC transporter ATP-binding protein

Query= TCDB::Q97VF4
         (324 letters)



>NCBI__GCF_000420385.1:WP_022670625.1
          Length = 326

 Score =  214 bits (546), Expect = 2e-60
 Identities = 125/327 (38%), Positives = 193/327 (59%), Gaps = 18/327 (5%)

Query: 3   LMELKGVSVIFEDK----VGLFKKRK--FYALKDVSLSMNQGDLLIVLGESGAGKTTLGR 56
           ++E+K +   FE K       F K K    A+ DVS S+ +G+ L ++GESG+GKTTLGR
Sbjct: 4   ILEVKNLKKEFELKGSWLASFFSKDKPTVKAVDDVSFSIRKGETLGIVGESGSGKTTLGR 63

Query: 57  VIVGLQKPTSGEVVYDGYNIWKNKRKIFKKYRKDVQLIPQDPYSTLPFNKTVEEILVAPI 116
            ++ L +PT+G +++ G ++ K  +   +K RK+ Q+I QDP ++L     + +I+  P+
Sbjct: 64  TVLRLTEPTAGSIIFKGKDLAKLPKSELRKERKNFQIIFQDPMASLNPYMRIGKIVSHPL 123

Query: 117 LRWEKINKDELRKRLINLLELVKLTPAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIV 176
                  K+E ++R++ L E + L+PAEEF  ++P  LSGGQ+QR+ IAR+L  NP  IV
Sbjct: 124 EIHNIGTKNERKERILELFEKINLSPAEEFYNRFPKHLSGGQRQRVVIARALITNPEFIV 183

Query: 177 ADEPVTMVDASLRIGILNTLAEIKNRLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGR 236
           ADEP  M+D S+R  IL  + ++K    LT +FITHD+  A+Y           VM+ G+
Sbjct: 184 ADEPTAMLDVSVRSQILKLMIDVKETFGLTYLFITHDLASAKYICDRIG-----VMYLGK 238

Query: 237 IVERADLEEILKDPLHPYTNDLIKLTPSID-NLYKEINVK----INYERVEKGCPYRLRC 291
           IVE A   ++ K+PLHPYT  L+   P  D N+ +E  +      +  ++  GC +  RC
Sbjct: 239 IVEIAKTFDLFKEPLHPYTKILMSSVPIPDPNIRREKLLPKGEIPSATKIPSGCRFHTRC 298

Query: 292 PFAMDICKNEEPKLFKYSHE--VACFL 316
           PFA +IC  +EP+L +   +  VAC L
Sbjct: 299 PFAKEICSQKEPELKEIEKDRFVACHL 325


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: 327
Number of extensions: 10
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: 326
Length adjustment: 28
Effective length of query: 296
Effective length of database: 298
Effective search space:    88208
Effective search space used:    88208
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 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