GapMind for catabolism of small carbon sources

 

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

Align 2-Deoxy-D-ribose porter, DeoP (characterized)
to candidate N515DRAFT_1918 N515DRAFT_1918 MFS transporter, FHS family, L-fucose permease

Query= TCDB::Q8XEV7
         (438 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1918
          Length = 442

 Score =  208 bits (529), Expect = 3e-58
 Identities = 124/411 (30%), Positives = 224/411 (54%), Gaps = 9/411 (2%)

Query: 24  LLSCLFPLWGCAAALNDILITQFKSVFSLSNFASALVQSAFYGGYFLIAIPASLVIKKTS 83
           +L+ +F +WG    LNDILI   K+VF L+   + LVQ  F+G YFL+++PA L++ +  
Sbjct: 31  VLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLVARLG 90

Query: 84  YKVAILIGLTLYIVGCTLFFPASHMATYTMFLAAIFAIAIGLSFLETAANTYSSMIGPKA 143
           YK  I+ GL +  VG   F+PA+ M  Y  FL A+F +A G++ L+ AAN Y +++GP+ 
Sbjct: 91  YKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALLGPEK 150

Query: 144 YATLRLNISQTFYPIGAAAGILLGKYLVFSEGESLEKQMAGMNAEQVHNFKVLMLENTLE 203
            A+ RL ++Q    +G       G  L+ S      +Q+A ++  +   ++V   +    
Sbjct: 151 SASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQEAQTVQG 210

Query: 204 PYKYMIMVLVVVMVLFLLTRFPT-CKVAQTASHKRPSALDTLRYLASNARFRRGIVAQFL 262
           PY  + +VL ++ V   L R P   +  + AS K+ S +  LR+         G++A F 
Sbjct: 211 PYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSLVSPLRH----PHVLFGVLAIFF 266

Query: 263 YVGMQVAVWSFTIRLAL--ELGDINERDASTFMVYSFACFFIGKFIANILMTRFNPEKVL 320
           YVG +VA+ SF +      ++G+++E+ A+ ++ Y +    IG+FI + L+ + +P K+L
Sbjct: 267 YVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRKLL 326

Query: 321 ILYSVIGALFLAYVALAPSFSAVYVAVLVSVLFGPCWATIYAGTLDTVDNEHTEMAGAVI 380
            +++ I    +    +     A+Y  V + +     + TI++  ++ +    T  A +++
Sbjct: 327 AIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERM-GPMTGEASSLL 385

Query: 381 VMAIVGAAVVPAIQGYVADMFHSLQLSFLVSMLCFVYVGVYFWRESKVRGN 431
           +MAIVG A+VP +QG  AD    +Q +F + +LC+ Y+  Y    S+++ +
Sbjct: 386 IMAIVGGAIVPFVQGLFADHI-GVQHAFFLPLLCYAYIVFYGLYGSRIKSD 435


Lambda     K      H
   0.329    0.139    0.412 

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: 414
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: 438
Length of database: 442
Length adjustment: 32
Effective length of query: 406
Effective length of database: 410
Effective search space:   166460
Effective search space used:   166460
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 (21.8 bits)
S2: 51 (24.3 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