GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruF in Collimonas arenae Ter10

Align Fructose import permease protein FruF (characterized)
to candidate WP_061533692.1 CAter10_RS12715 ABC transporter permease

Query= SwissProt::Q8G846
         (356 letters)



>NCBI__GCF_001584165.1:WP_061533692.1
          Length = 374

 Score =  218 bits (554), Expect = 3e-61
 Identities = 132/341 (38%), Positives = 198/341 (58%), Gaps = 22/341 (6%)

Query: 25  IVAFILLVIICTIFQHDFLALSWNSNTGGLAGPLITMLQESARYLMIATGMTLVISTAGI 84
           + A  LL+ I       F  + W    G L G LI ++  +A  ++ A GMTLVI+T GI
Sbjct: 42  LAALALLLAIDFFVIPGFFRMEWKD--GHLYGSLIDIVNRAAPLILTALGMTLVIATRGI 99

Query: 85  DLSVGSVMAVAGAAAMQTLS------NGMNVWLSIL-----IALAVGLAI--GCVNGALV 131
           D+SVG+V+A++G      +       NG+  ++S +     IA A+G AI  G  NG LV
Sbjct: 100 DISVGAVVAISGTVIALLIGGNVEMHNGVPQYVSQIPMGWAIAAAMGAAILCGAWNGFLV 159

Query: 132 SFLGLQPFITTLIMMLAGRGMAKVITSGENTDASAVAGNEPLKWFANGFILGIPANFVIA 191
           + LGLQP I TLI+M+ GRG+A+++T G+          +P  +  +G++ G+P +  IA
Sbjct: 160 ATLGLQPIIATLILMVGGRGLAQLLTDGQ----IITVYYKPFFYLGSGYLFGLPFSLFIA 215

Query: 192 VIIVILVGLLCRKTAMGMMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAAIAGLFAT 251
           + + ++V LL RKTA+G+ I+AVGIN  A+R+ GI+   ++F VY      A +AGL  +
Sbjct: 216 IGVFLIVALLMRKTALGLFIQAVGINPVAARLAGIRTAALIFFVYIFCSACAGVAGLLIS 275

Query: 252 ASVMRVDVVKTGQDLEMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKTIITLGVN 311
           +++   D    G  LE+ AILAV +GGTSL GGKFSL GS +GA+II  +  TI ++GV 
Sbjct: 276 SNIKSADANNAGLLLELDAILAVTLGGTSLAGGKFSLVGSVIGALIIQTLTYTIYSMGVP 335

Query: 312 AEATPAFFAVVVIVICVMQAPKIHNLSANMKRKRALKAQAK 352
            E      ++VV  +C+ Q+P+  +L    KR     AQ K
Sbjct: 336 PEVNMVVKSIVVFAVCLSQSPEFRHL---WKRLFGASAQEK 373


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: 340
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: 374
Length adjustment: 30
Effective length of query: 326
Effective length of database: 344
Effective search space:   112144
Effective search space used:   112144
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 24 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