GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Desulfovibrio vulgaris Miyazaki F

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate 8501089 DvMF_1825 oligopeptide/dipeptide ABC transporter, ATPase subunit (RefSeq)

Query= TCDB::Q97VF4
         (324 letters)



>FitnessBrowser__Miya:8501089
          Length = 339

 Score =  177 bits (449), Expect = 3e-49
 Identities = 107/305 (35%), Positives = 168/305 (55%), Gaps = 22/305 (7%)

Query: 21  KKRKFYALKDVSLSMNQGDLLIVLGESGAGKTTLGRVIVGLQKPTSGEVVYDGYNIWKNK 80
           K+   +A+ DVS  +  G+ L V+GESG GK+TL R ++GL + T GE++Y G  I    
Sbjct: 38  KRTVVHAVNDVSFDILPGETLSVVGESGCGKSTLARTVIGLYRATGGEILYRGERIDNLS 97

Query: 81  RKIFKKYRKDVQLIPQDPYSTLPFNKTVEEILVAPILRWEK--INKDELRKRLINLLELV 138
                 YR  +Q++ QDPY++L     V EIL  P+ R+    I+  ++R R+ +++E V
Sbjct: 98  DNGMLPYRTRMQMVFQDPYASLNPRMKVREILEEPV-RFHNPGISDADVRARVADVMEQV 156

Query: 139 KLTPAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIVADEPVTMVDASLRIGILNTLAE 198
            + P      +YPH+ SGGQ+QR+SIAR+L V+P  IVADEP++ +D S++  +LN + +
Sbjct: 157 GVNPLWGV--RYPHEFSGGQRQRISIARALVVDPEFIVADEPISALDVSIQAQVLNLMMD 214

Query: 199 IKNRLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGRIVERADLEEILKDPLHPYTNDL 258
           ++ + NLT +FI+HD+ +  +           VM+ G + E A  E++  +P HPYT  L
Sbjct: 215 MQEKRNLTYLFISHDLSVVEHI-----STRVAVMYLGSLCELASAEDLFGNPRHPYTRAL 269

Query: 259 IKLTPSID-------NLYKEINVKINYERVEKGCPYRLRCPFAMDICKNEEPKL--FKYS 309
           +   P I         L  ++   IN   +  GC +  RC  A   C  E PK    +  
Sbjct: 270 LSAIPRIGGKAAGHIKLSGDVPTPIN---LPTGCVFHGRCQHANARCMQEVPKARQLEGG 326

Query: 310 HEVAC 314
            +VAC
Sbjct: 327 AQVAC 331


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: 297
Number of extensions: 16
Number of successful extensions: 5
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: 339
Length adjustment: 28
Effective length of query: 296
Effective length of database: 311
Effective search space:    92056
Effective search space used:    92056
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