GapMind for catabolism of small carbon sources

 

Aligments 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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