GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruF in Paraburkholderia bryophila 376MFSha3.1

Align Fructose import permease protein FruF (characterized)
to candidate H281DRAFT_05271 H281DRAFT_05271 monosaccharide ABC transporter membrane protein, CUT2 family

Query= SwissProt::Q8G846
         (356 letters)



>FitnessBrowser__Burk376:H281DRAFT_05271
          Length = 347

 Score =  225 bits (574), Expect = 1e-63
 Identities = 134/326 (41%), Positives = 197/326 (60%), Gaps = 11/326 (3%)

Query: 21  LTWSIVAFILLVIICTIFQHDFLALSWNSNTGGLAGPLITMLQESARYLMIATGMTLVIS 80
           L W  V   LL  +       FL+L      G L G  I +L  +A  +++ATGMTLVI+
Sbjct: 16  LIWPCVTLALLCALNLWVNPHFLSLRMLD--GHLFGAPIDVLNRAAPLVLVATGMTLVIA 73

Query: 81  TAGIDLSVGSVMAVAGAAAM-----QTLSNGMNVWLSILIALAVGLAIGCVNGALVSFLG 135
           T GID+SVG+V+A+AGAAA      Q +  G  +  ++L AL VG+  G  NG LVSF+G
Sbjct: 74  TRGIDISVGAVVAIAGAAAATILATQPVPTGNLIAQALLAALIVGVLSGMWNGLLVSFVG 133

Query: 136 LQPFITTLIMMLAGRGMAKVITSGENTDASAVAGNEPLKWFANGFILGIPANFVIAVIIV 195
           +QP I TLI+M+AGRG+A+++T+G+     A        +   G+ LG+P +  IA I V
Sbjct: 134 MQPIIATLILMVAGRGIAQLLTAGQIIPIGAPG----YLFVGGGYWLGVPCSVWIATIAV 189

Query: 196 ILVGLLCRKTAMGMMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAAIAGLFATASVM 255
           +    L   TA+G+ I A+G+N  A+R+ G++ K ++F VY  SG  AA+AG+  +++V 
Sbjct: 190 LATAALVEGTALGLFIRAIGVNPVATRLVGLRSKALVFAVYGFSGLTAAMAGILISSNVR 249

Query: 256 RVDVVKTGQDLEMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKTIITLGVNAEAT 315
             D    G  LE+ AILAV +GGTSLLGG+FS AG+ +GA+II  +  T  ++GV  EAT
Sbjct: 250 SADGNNAGLLLELDAILAVTLGGTSLLGGRFSFAGTVLGALIIQTLTYTTYSIGVPPEAT 309

Query: 316 PAFFAVVVIVICVMQAPKIHNLSANM 341
               A VV+ + V+Q+P    L+ ++
Sbjct: 310 LVVKAAVVLTVSVIQSPAARALAMSV 335


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: 324
Number of extensions: 21
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: 356
Length of database: 347
Length adjustment: 29
Effective length of query: 327
Effective length of database: 318
Effective search space:   103986
Effective search space used:   103986
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