GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12055 in Pseudomonas simiae WCS417

Align Putative xylitol transport system substrate-binding protein; SubName: Full=Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate GFF2170 PS417_11070 rhizopine-binding protein

Query= uniprot:A0A1N7UEK0
         (335 letters)



>FitnessBrowser__WCS417:GFF2170
          Length = 308

 Score =  166 bits (420), Expect = 7e-46
 Identities = 98/290 (33%), Positives = 166/290 (57%), Gaps = 14/290 (4%)

Query: 11  AALSLLACSIAMAADGKTYKVGAAVYGLKGQFMQNWVRELKEHPAVKDGTVQLTVFDGNY 70
           A L LL    + AA    Y++G ++  +   FM  +VR   E  A +   VQ+   D   
Sbjct: 9   ATLLLLFSQWSFAA----YRIGVSIARVDDNFM-TYVRTGLE-AAARQQDVQIQFEDAQG 62

Query: 71  DALTQNNQIENMVTQRYDAILFVPIDTKAGVGTVKAAMSNDVVVIASNTKVADASVPY-- 128
           D + Q NQ+E  + Q+ DA++ +P+DT A     +AA++    ++  N    + ++P   
Sbjct: 63  DVVRQLNQVEGFLNQKVDAVIVLPVDTAATANMTRAAVAAKTPLVYVNRHPDERTLPKGV 122

Query: 129 --VGNDDVEGGRLQAQAMVDKLNGKGNVVIIQGPIGQSAQIDREKGELEVLGKHPDIKII 186
             V ++D+E G+LQ + + +KL GKGNV II G + Q+A  DR +G  +VL   P IK++
Sbjct: 123 VTVASNDIEAGQLQMRYLAEKLAGKGNVAIIMGDLAQNATHDRTEGAKQVLKDFPGIKVV 182

Query: 187 EKKTANWDRAQALALTEDWLNAHPKGINGVIAQNDDMALGAVQALKSHGLTSKDVPVTSI 246
           E+++A+W R++ + LT +WL A  +  + ++A ND+MA+GA  AL+  G    DV +  I
Sbjct: 183 EQQSADWQRSKGMDLTSNWLLAGTQ-FDAIVANNDEMAIGAAMALQQAGKAKGDVAIVGI 241

Query: 247 DGMPDAIQAAKKDEVT-TFLQDAQAQSQGALDVALRALAGKDYKPQSVIW 295
           DG+PD + A K+  +T +  QD +AQ+  A+  A+R + G+  +P+  +W
Sbjct: 242 DGLPDGLAAIKRGLLTASVFQDPKAQATQAVQAAVRMIKGEAIEPE--VW 289


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: 257
Number of extensions: 12
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.

Links

Downloads

Related tools

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