GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Collimonas arenae Ter10

Align Fructose import permease protein FruG (characterized)
to candidate WP_061535202.1 CAter10_RS06725 hypothetical protein

Query= SwissProt::Q8G845
         (340 letters)



>NCBI__GCF_001584165.1:WP_061535202.1
          Length = 330

 Score =  162 bits (410), Expect = 1e-44
 Identities = 105/312 (33%), Positives = 167/312 (53%), Gaps = 11/312 (3%)

Query: 20  RQMIPTLAAVVIFILMIIMGQALFGTYIRLGFISSLFIDHAYLIILAVAMTLPILTGGID 79
           R ++ T+  + + +L+I+    L   +  L  +S +    +  I+LA  MT  ILT GID
Sbjct: 21  RNLMRTVGMLPVLLLLILGFSLLSQNFFTLQNLSIVTQQASVNIVLAAGMTFVILTAGID 80

Query: 80  LSVGAIVAITAVVGLKLANAGVPAFLVMIIMLLIGAVFGLLAGTLIEEFNMQPFIATLST 139
           LSVGAI+A +AVV +  + +     L +   L  G + GL+ G LI    + PFI TL  
Sbjct: 81  LSVGAILAASAVVAMLASMSPQYGMLGIAAGLGFGLLLGLVNGVLIAFMRLPPFIVTLGA 140

Query: 140 MFLARGLASIISTDSLTFPQGNDFSFISNVIKIIDNPKISNDLSFNVGVIIALVVVVFGY 199
           +   RGLA +++ D   F     F+FI N   I+  P +         VIIAL+VV   +
Sbjct: 141 LTAMRGLARLLADDKTVFNPELPFAFIGN-DSILGVPWL---------VIIALLVVALAW 190

Query: 200 VFLHHTRTGRTIYAIGGSRSSAELMGLPVKRTQYIIYLTSATLAALASIVYTANIGSAKN 259
             L  T  G  IYA+GG+  +A L G+ V +    +Y  S  LA L +++  + + +A  
Sbjct: 191 FILRRTVIGVQIYAVGGNAEAARLSGIKVWKVLLFVYAVSGLLAGLGAVMTASRLSAANG 250

Query: 260 -TVGVGWELDAVASVVIGGTIITGGFGYVLGSVLGSLVRSILDPLTSDFGVPAEWTTIVI 318
             +G  +ELDA+A+V++GGT  TGG G ++G+++G+L+ ++L       GV   W  I+ 
Sbjct: 251 LQLGQSYELDAIAAVILGGTSFTGGVGSIVGTLIGALIIAVLTNGLVLLGVSDIWQYIIK 310

Query: 319 GLMILVFVVLQR 330
           G++I+  V L R
Sbjct: 311 GIVIIGAVALDR 322


Lambda     K      H
   0.327    0.142    0.400 

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: 265
Number of extensions: 13
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: 340
Length of database: 330
Length adjustment: 28
Effective length of query: 312
Effective length of database: 302
Effective search space:    94224
Effective search space used:    94224
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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