GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruF in Dyella japonica UNC79MFTsu3.2

Align Fructose import permease protein FruF (characterized)
to candidate N515DRAFT_2414 N515DRAFT_2414 simple sugar transport system permease protein

Query= SwissProt::Q8G846
         (356 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2414
          Length = 358

 Score =  217 bits (552), Expect = 4e-61
 Identities = 126/339 (37%), Positives = 193/339 (56%), Gaps = 11/339 (3%)

Query: 13  VKKLLSSNLTWSIVAFILLVIICTIFQHDFLALSWNSNTGGLAGPLITMLQESARYLMIA 72
           +++ L+  L W ++  ILL+    +F   FLAL W    G L G LI +   +A   +++
Sbjct: 22  LRRCLAHPLLWPLLTLILLLAGNGLFNPGFLALQWRD--GHLYGNLIDIAHRAAPLALVS 79

Query: 73  TGMTLVISTAGIDLSVGSVMAVAGAAAMQTLSNGMN-----VWLSILIALAVGLAIGCVN 127
            GMTLVI+  G+D+SVG+V+A+A   A  T+ +  N     +WL+I  ALA G   G  N
Sbjct: 80  LGMTLVIALRGLDISVGAVLAIAATVAAWTIGHVSNDGLLPLWLAIAAALAAGALCGLWN 139

Query: 128 GALVSFLGLQPFITTLIMMLAGRGMAKVITSGENTDASAVAGNEPLKWFANGFILGIPAN 187
           G LV   G+QP + TLI+M+AGRG+A+ I+ G+           P  +  NGF+LG+P +
Sbjct: 140 GWLVVGAGMQPIVATLILMVAGRGIAQSISGGQILTLYYA----PYSFLGNGFVLGLPFS 195

Query: 188 FVIAVIIVILVGLLCRKTAMGMMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAAIAG 247
             +   +  L+ L  RKTA+G+ + A+G N +A+ + G++ + I    Y   G  AA+AG
Sbjct: 196 LFVVAAVFALLQLALRKTALGLFVRAIGHNPQAAHVAGVRARAITLGAYVFCGIAAALAG 255

Query: 248 LFATASVMRVDVVKTGQDLEMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKTIIT 307
           L  +++V   D    G  LE+ AILAV +GG+ L GG+FSLAGS +GA+II  +  TI  
Sbjct: 256 LLVSSNVNSADANNAGLLLELDAILAVALGGSLLGGGRFSLAGSLLGALIIQALTTTIYA 315

Query: 308 LGVNAEATPAFFAVVVIVICVMQAPKIHNLSANMKRKRA 346
           +GV  +   A  AV+V  + ++Q+P        + R RA
Sbjct: 316 IGVPPQVNLAVKAVLVFAVMLLQSPLCRGQLRALLRLRA 354


Lambda     K      H
   0.325    0.136    0.384 

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: 350
Number of extensions: 20
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: 356
Length of database: 358
Length adjustment: 29
Effective length of query: 327
Effective length of database: 329
Effective search space:   107583
Effective search space used:   107583
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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