GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Desulfovibrio vulgaris Miyazaki F

Align MsiK protein, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized)
to candidate 8502259 DvMF_2969 ABC transporter related (RefSeq)

Query= TCDB::P96483
         (377 letters)



>FitnessBrowser__Miya:8502259
          Length = 418

 Score =  215 bits (547), Expect = 2e-60
 Identities = 119/293 (40%), Positives = 173/293 (59%), Gaps = 4/293 (1%)

Query: 20  AVDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIRIGDRDVTHLPPKDRDI 79
           AV+ +   +E G F  ++GPSGCGK+T LRM+AG E  + G I I  RD+  + P  R +
Sbjct: 43  AVNDVSFEVEQGRFFSILGPSGCGKTTLLRMIAGFESPDSGVIAIRGRDMAGIAPNRRPV 102

Query: 80  AMVFQNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEAAKILDLTQYLDRKPKALSGG 139
            ++FQ+ AL+P M+VA+N+ F LK  G+   EI ++V++  + + L  Y  + P  LSGG
Sbjct: 103 NLIFQHLALFPMMSVAENVAFGLKRRGMAGGEISRRVQDVLERVGLPGYGVKMPAQLSGG 162

Query: 140 QRQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVTHDQVEA 199
           Q+QRVA+ R +V EP V L+DEPL  LD KLR   + ++ +LQ  +G T VY+THDQ EA
Sbjct: 163 QKQRVAIARCLVLEPAVLLLDEPLGALDLKLREQMKVELKTLQAEVGTTFVYITHDQSEA 222

Query: 200 MTMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAM--NLVEVPITDGGVKFGN 257
           + M D VAV+  G  +QVD+PRN+Y +PA+ FVAGF+G   +    +E    D G+   +
Sbjct: 223 LVMSDHVAVMNAGRFEQVDTPRNLYRRPASAFVAGFVGETNVWSGTLEEATGDAGLVRTD 282

Query: 258 SVVPVNREALSAADKGDRTVTVGVRPEHFDVVELGGAVAASLSKDSA-DAPAG 309
                     +   KG R V + +RPE   +   G + A   + D A D  AG
Sbjct: 283 EGAVFRARVAAGLAKGTR-VDMFIRPEAVLIDPDGASCATDGATDGATDGAAG 334


Lambda     K      H
   0.317    0.135    0.379 

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: 431
Number of extensions: 22
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 377
Length of database: 418
Length adjustment: 31
Effective length of query: 346
Effective length of database: 387
Effective search space:   133902
Effective search space used:   133902
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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