GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfQ in Acidovorax sp. GW101-3H11

Align Galactofuranose-binding protein YtfQ (characterized)
to candidate Ac3H11_611 Putative sugar ABC transport system, periplasmic binding protein YtfQ precursor

Query= SwissProt::P39325
         (318 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_611
          Length = 322

 Score =  307 bits (787), Expect = 2e-88
 Identities = 169/316 (53%), Positives = 223/316 (70%), Gaps = 15/316 (4%)

Query: 11  VSAAMSSMALAA----------PLTVGFSQVGSESGWRAAETNVAKSEAEKRGITLKIAD 60
           V+AA++S+ +AA          PL +GFSQVG+ES WR A T   KS A++ GI LK +D
Sbjct: 9   VAAALASVPVAALLPSTAWAQKPLVLGFSQVGAESEWRTANTESIKSAAKEAGIELKFSD 68

Query: 61  GQQKQENQIKAVRSFVAQGVDAIFIAPVVATGWEPVLKEAKDAEIPVFLLDRSIDVKDKS 120
            QQKQENQIKA+RSF+AQ VD I  +PVV +GWEPVL+EAK A+IPV L DR+++ KD S
Sbjct: 69  AQQKQENQIKAIRSFIAQKVDVIAFSPVVESGWEPVLREAKAAKIPVVLTDRAVNTKDTS 128

Query: 121 LYMTTVTADNILEGKLIGDWLVKEVNGK--PCNVVELQGTVGASVAIDRKKGFAEAIKNA 178
           LY+T + +D + EG+  G WLV+++  +    N+VELQGTVG++ AIDRKKGF E IK  
Sbjct: 129 LYVTFMGSDFVEEGRKAGRWLVEKMKDQKGEVNIVELQGTVGSAPAIDRKKGFEEIIKAD 188

Query: 179 PNIKIIRSQSGDFTRSKGKEVMESFIKAENNGKNICMVYAHNDDMVIGAIQAIKEAGLKP 238
           P  KIIRSQ+GDFTR+KGKEVME+F+KAE  GK I ++YAHNDDM IGAIQAI+EAG+KP
Sbjct: 189 PKFKIIRSQTGDFTRAKGKEVMEAFLKAE--GKKINVLYAHNDDMAIGAIQAIEEAGMKP 246

Query: 239 GKDILTGSIDGVPDIYKAMMDGEANASVELTPNMAGPAFDALEKYKKDGTMPEKLTLTKS 298
            KDI+  SID V   ++AM+ G+ N SVE +P + GP   A  K  K G    K  +T+ 
Sbjct: 247 AKDIVIISIDAVKGAFEAMIAGKLNVSVECSP-LLGPQLMAAVKDIKAGKAVPKRIVTEE 305

Query: 299 TLYLPDTAKEELEKKK 314
            ++  + A +E+  +K
Sbjct: 306 GIFPMEVAAKEMPNRK 321


Lambda     K      H
   0.313    0.130    0.363 

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: 308
Number of extensions: 15
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: 318
Length of database: 322
Length adjustment: 28
Effective length of query: 290
Effective length of database: 294
Effective search space:    85260
Effective search space used:    85260
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