GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruF in Burkholderia phytofirmans PsJN

Align Fructose import permease protein FruF (characterized)
to candidate BPHYT_RS23880 BPHYT_RS23880 sugar ABC transporter permease

Query= SwissProt::Q8G846
         (356 letters)



>FitnessBrowser__BFirm:BPHYT_RS23880
          Length = 343

 Score =  229 bits (585), Expect = 6e-65
 Identities = 136/341 (39%), Positives = 205/341 (60%), Gaps = 11/341 (3%)

Query: 10  NNFVKKLLSSNLTWSIVAFILLVIICTIFQHDFLALSWNSNTGGLAGPLITMLQESARYL 69
           N FV+      L W  V  +LL  +       FL+L      G L G  I +L  +A  +
Sbjct: 5   NWFVRDGAERPLIWPCVTLVLLCGLNLWVNPHFLSLRMLD--GHLFGAPIDVLNRAAPLV 62

Query: 70  MIATGMTLVISTAGIDLSVGSVMAVAGAAAMQTLS-----NGMNVWLSILIALAVGLAIG 124
           ++ATGMTLVI+T GID+SVG+V+A+AGAAA   L+     +   +  +++ AL VG+  G
Sbjct: 63  LVATGMTLVIATRGIDISVGAVVAIAGAAAATILAAQPEPSSALIAQALIAALIVGVLSG 122

Query: 125 CVNGALVSFLGLQPFITTLIMMLAGRGMAKVITSGENTDASAVAGNEPLKWFANGFILGI 184
             NG LVSF+G+QP I TLI+M+AGRG+A+++T+G+     A        +   G++LG+
Sbjct: 123 MWNGVLVSFVGMQPIIATLILMVAGRGIAQLLTAGQIIPIGAPG----YLFVGGGYLLGV 178

Query: 185 PANFVIAVIIVILVGLLCRKTAMGMMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAA 244
           P++  IA + V+    L   TA+G+ I A+G+N  A+R+ G++ K ++F VY  SG  AA
Sbjct: 179 PSSVWIATVAVLATAALVEGTALGLFIRAIGVNPVATRLVGLRSKALVFAVYGFSGLTAA 238

Query: 245 IAGLFATASVMRVDVVKTGQDLEMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKT 304
           +AG+  +++V   D    G  LE+ AILAV +GGTSLLGG+FSLAG+ +GA+II  +  T
Sbjct: 239 MAGILISSNVRSADGNNAGLLLELDAILAVTLGGTSLLGGRFSLAGTVLGALIIQTLTYT 298

Query: 305 IITLGVNAEATPAFFAVVVIVICVMQAPKIHNLSANMKRKR 345
             ++GV  EAT    A VV+ + V+Q+P    L  ++   R
Sbjct: 299 TYSIGVPPEATLVVKAAVVLAVSVIQSPSARALGMSLVTHR 339


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: 331
Number of extensions: 19
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: 343
Length adjustment: 29
Effective length of query: 327
Effective length of database: 314
Effective search space:   102678
Effective search space used:   102678
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