GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11885 in Pseudomonas simiae WCS417

Align Inositol transport system sugar-binding protein (characterized)
to candidate GFF2675 PS417_13645 ABC transporter

Query= reanno::WCS417:GFF2331
         (309 letters)



>FitnessBrowser__WCS417:GFF2675
          Length = 310

 Score =  150 bits (379), Expect = 4e-41
 Identities = 102/303 (33%), Positives = 161/303 (53%), Gaps = 13/303 (4%)

Query: 7   FTALALSMLLASGVASAADLKIGVSMSAFDDTFLTYLREDMDKQAKSYPKGDGVQLQFED 66
           F  +AL+ L++  V +     +G+SM +  + +   L +    +AK       V++    
Sbjct: 7   FPVIALAALMSQAVEARELKALGISMGSLGNPYFVTLADGATARAKEL--NPNVKVTSVS 64

Query: 67  ARADVVKQLSQVENFISQKVDAIIVNPVDTASTANIIKAATAAKIPLVFVNRRPDSQTLA 126
           A  D+ KQ SQ++NFIS KVD I++N VD ++ A+ IK A  A I +V V+        A
Sbjct: 65  ADYDLSKQFSQIDNFISSKVDLILINAVDPSAMASAIKKARDAGIVVVAVD------VDA 118

Query: 127 PGV-AAVTSDDVEAGKLQMQYIAEKLGGKGNIVILLGDLANNSTTNRTKGVKEVLTKYPG 185
            GV A V +D+VEAGKL  QY+ +KL GKGN++I  G     + T+R KG K  L   P 
Sbjct: 119 KGVNATVQTDNVEAGKLACQYLVDKLSGKGNVIIQNGPQV-TAVTDRVKGCKAALAAAPD 177

Query: 186 IKI-EQEQTGIWLRDRGMTLVNDWLTQGRDFQAVLSNNDEMAIGAAMALKSAGKKGVLIA 244
           IK+   +Q G   R+ G+ ++  +LT+      + + ND  A+G+ +A K   + G++I 
Sbjct: 178 IKVLSDDQDGKGSREGGLNVMQGYLTRFPKIDGLFAINDPQAVGSDLAAKQLKRSGLIIT 237

Query: 245 GVDGTPDGLNAI-TKGDMTVSAFQDAKGQADKSVETARKMAKNE-PIEQNVVIPFQLITP 302
            VDG PD  NA+ T   +  S+ QD    A  +V     +  ++ P E   ++  +LIT 
Sbjct: 238 SVDGAPDIENALKTDSQIQASSSQDPWAMAQTAVNVGNDILNDKAPAEAVTLLTPKLITR 297

Query: 303 DNV 305
           DN+
Sbjct: 298 DNI 300


Lambda     K      H
   0.314    0.131    0.357 

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: 217
Number of extensions: 14
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: 309
Length of database: 310
Length adjustment: 27
Effective length of query: 282
Effective length of database: 283
Effective search space:    79806
Effective search space used:    79806
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 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