GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF_Tm in Dyella japonica UNC79MFTsu3.2

Align ABC-type transporter, integral membrane subunit, component of Xylose porter (Nanavati et al. 2006). Regulated by xylose-responsive regulator XylR (characterized)
to candidate N515DRAFT_3233 N515DRAFT_3233 xylose ABC transporter membrane protein

Query= TCDB::Q9WXW7
         (317 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3233
          Length = 380

 Score =  159 bits (401), Expect = 1e-43
 Identities = 121/366 (33%), Positives = 188/366 (51%), Gaps = 65/366 (17%)

Query: 10  FRELGPLVALVSLAVFTAILNPR-FLTAFNLQALGRQIAIFGLLAIGETFVIISGGGAID 68
           ++ L  L+A+ ++ VF  +     F+TA N+  L RQ+AI G+LA G  FVII+G   ID
Sbjct: 13  YKILALLLAVAAIWVFFHVATGGDFVTARNVSNLFRQMAITGMLACGMVFVIIAG--EID 70

Query: 69  LSPGSMVALTGVMVAWLMTH---GVPV------------------WISVILILLFSIGAG 107
           LS GS++ L G +VA L  +     PV                  W++ + +  F +G G
Sbjct: 71  LSVGSLLGLLGGVVAVLTVNQGWSTPVAIVAVLGLGVLIGLFNGFWVTRLRVPSFIVGLG 130

Query: 108 ---AWHGLFV------TKLRVPAFIITLG--------TLTIARGMAAVITKGWPIIGLPS 150
              A+ G+ +      T   VPA ++ LG        +  +   + AV+     +     
Sbjct: 131 GMLAFRGVLLGTTHSATIAPVPADLVYLGQGYVSPLWSTVLGVAIFAVVVALAVLRRRRR 190

Query: 151 SFLKIGQ----GEFLK--------------------IPIPVWILLAVALVADFFLRKTVY 186
           + L+I Q     + LK                    IP+PV IL+A+  V  +   +TV 
Sbjct: 191 AQLQIRQLPWWADLLKVVAIGAALGVFVATLNSYGGIPLPVLILVALLAVFSYLASQTVL 250

Query: 187 GKHLRASGGNEVAARFSGVNVDRVRMIAFMVSGFLAGVVGIIIAARLSQGQPGVGSMYEL 246
           G+H+ A GGN  A R SGVNV RV+++ F + G +    GI+  ARL+ G P  G+  EL
Sbjct: 251 GRHIYAVGGNLEATRLSGVNVARVKLVVFGIMGLMCAFAGIVNTARLAAGSPSAGTNGEL 310

Query: 247 YAIASTVIGGTSLTGGEGSVLGAIVGASIISLLWNALVLLNVSTYWHNVVIGIVIVVAVT 306
            AIA+  IGG S+ GG G+V GA++GA +++ L N + +++V TYW  +V G ++V+AV 
Sbjct: 311 DAIAACFIGGASMRGGAGTVHGALIGALVMASLDNGMSMMDVDTYWQYIVKGAILVLAVW 370

Query: 307 LDILRR 312
           +D+L R
Sbjct: 371 VDVLSR 376


Lambda     K      H
   0.328    0.143    0.424 

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: 407
Number of extensions: 32
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 317
Length of database: 380
Length adjustment: 29
Effective length of query: 288
Effective length of database: 351
Effective search space:   101088
Effective search space used:   101088
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 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