GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12055 in Pseudomonas fluorescens FW300-N2E2

Align Putative xylitol transport system substrate-binding protein; SubName: Full=Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate Pf6N2E2_1793 Inositol transport system sugar-binding protein

Query= uniprot:A0A1N7UEK0
         (335 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1793
          Length = 308

 Score =  164 bits (416), Expect = 2e-45
 Identities = 100/291 (34%), Positives = 161/291 (55%), Gaps = 14/291 (4%)

Query: 1   MKLGTTLAATAALSLLACSIAMAADGKTYKVGAAVYGLKGQFMQNWVRELKEHPAVKDGT 60
           M+  T L AT    LL  S   AAD   Y++G ++  +   FM      L E  A K   
Sbjct: 1   MRRCTLLFATL---LLLFSQWAAAD---YRIGVSIARVDDNFMTYVRNGLAE--AAKKEN 52

Query: 61  VQLTVFDGNYDALTQNNQIENMVTQRYDAILFVPIDTKAGVGTVKAAMSNDVVVIASNTK 120
           VQ+   D   D + Q NQ++  + Q+ DA++ +P+DT A     +AA+     ++  N  
Sbjct: 53  VQIQFEDAQGDVVRQLNQVQGFINQKVDAVIVLPVDTSATANITRAAVEAKTPLVYVNRH 112

Query: 121 VADASVPY----VGNDDVEGGRLQAQAMVDKLNGKGNVVIIQGPIGQSAQIDREKGELEV 176
             + ++P     V ++D+E G LQ + + +KL GKGN+ II G + Q+A  DR +G  +V
Sbjct: 113 PDERTLPKGVVTVASNDIEAGHLQMRYLAEKLGGKGNLAIIMGDLAQNATHDRTEGVKQV 172

Query: 177 LGKHPDIKIIEKKTANWDRAQALALTEDWLNAHPKGINGVIAQNDDMALGAVQALKSHGL 236
           L  +P IKI+E+++A W R + + LT +WL A  +  + ++A ND+MA+GA  AL+  G 
Sbjct: 173 LKDYPGIKIVEQQSAEWQRNKGMDLTSNWLLAGSR-FDAIVANNDEMAIGAAMALQQAGK 231

Query: 237 TSKDVPVTSIDGMPDAIQAAKKDE-VTTFLQDAQAQSQGALDVALRALAGK 286
           T  +V +  IDG+PD + A K+   V +  QD +AQ+  A+  AL+ + G+
Sbjct: 232 TKGEVAIVGIDGLPDGLAAIKRGMLVASVFQDPKAQATSAVQAALKMIKGE 282


Lambda     K      H
   0.314    0.130    0.373 

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: 244
Number of extensions: 10
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: 335
Length of database: 308
Length adjustment: 28
Effective length of query: 307
Effective length of database: 280
Effective search space:    85960
Effective search space used:    85960
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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