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 GFF2331 PS417_11885 rhizopine-binding protein

Query= uniprot:A0A1N7UEK0
         (335 letters)



>FitnessBrowser__WCS417:GFF2331
          Length = 309

 Score =  162 bits (409), Expect = 1e-44
 Identities = 104/303 (34%), Positives = 166/303 (54%), Gaps = 18/303 (5%)

Query: 1   MKLGTTLAATAALSLLACSIAMAADGKTYKVGAAVYGLKGQFM----QNWVRELKEHPAV 56
           MK      A A   LLA  +A AAD    K+G ++      F+    ++  ++ K +P  
Sbjct: 1   MKTPIRFTALALSMLLASGVASAAD---LKIGVSMSAFDDTFLTYLREDMDKQAKSYP-- 55

Query: 57  KDGTVQLTVFDGNYDALTQNNQIENMVTQRYDAILFVPIDTKAGVGTVKAAMSNDVVVIA 116
           K   VQL   D   D + Q +Q+EN ++Q+ DAI+  P+DT +    +KAA +  + ++ 
Sbjct: 56  KGDGVQLQFEDARADVVKQLSQVENFISQKVDAIIVNPVDTASTANIIKAATAAKIPLVF 115

Query: 117 SN----TKVADASVPYVGNDDVEGGRLQAQAMVDKLNGKGNVVIIQGPIGQSAQIDREKG 172
            N    ++     V  V +DDVE G+LQ Q + +KL GKGN+VI+ G +  ++  +R KG
Sbjct: 116 VNRRPDSQTLAPGVAAVTSDDVEAGKLQMQYIAEKLGGKGNIVILLGDLANNSTTNRTKG 175

Query: 173 ELEVLGKHPDIKIIEKKTANWDRAQALALTEDWLNAHPKGINGVIAQNDDMALGAVQALK 232
             EVL K+P IKI +++T  W R + + L  DWL    +    V++ ND+MA+GA  ALK
Sbjct: 176 VKEVLTKYPGIKIEQEQTGIWLRDRGMTLVNDWL-TQGRDFQAVLSNNDEMAIGAAMALK 234

Query: 233 SHGLTSKDVPVTSIDGMPDAIQAAKKDEVT-TFLQDAQAQSQGALDVALRALAGKDYKPQ 291
           S G   K V +  +DG PD + A  K ++T +  QDA+ Q+  +++ A R +A  +   Q
Sbjct: 235 SAG--KKGVLIAGVDGTPDGLNAITKGDMTVSAFQDAKGQADKSVETA-RKMAKNEPIEQ 291

Query: 292 SVI 294
           +V+
Sbjct: 292 NVV 294


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: 245
Number of extensions: 13
Number of successful extensions: 4
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: 309
Length adjustment: 28
Effective length of query: 307
Effective length of database: 281
Effective search space:    86267
Effective search space used:    86267
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