GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruP in Pantoea rwandensis LMG 26275

Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate WP_084933726.1 HA51_RS07045 L-fucose:H+ symporter permease

Query= uniprot:A0A1I2JXG1
         (442 letters)



>NCBI__GCF_002095475.1:WP_084933726.1
          Length = 441

 Score =  204 bits (519), Expect = 5e-57
 Identities = 121/401 (30%), Positives = 216/401 (53%), Gaps = 10/401 (2%)

Query: 31  VLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLVARLG 90
           +L+ +F +WG    LNDILI   K+VF L+   + LVQ  F+G YFL+++PA L++ +  
Sbjct: 23  LLSCLFPLWGCAASLNDILITQFKSVFALSDFASALVQSAFYGGYFLIAIPASLVIRKAT 82

Query: 91  YKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALLGPEK 150
           YK  I+ GL +  VG   F+PA+ M  Y  FL A+F +A G++ L+ AAN Y +++G   
Sbjct: 83  YKLAILMGLVLYIVGCVLFYPASHMATYTMFLAAIFAIAIGLSFLETAANTYSSMIGHRD 142

Query: 151 SASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQEAQTVQG 210
            A+ RL ++Q    +G  +    G  L+         Q+A ++  +  A+R+   +    
Sbjct: 143 HATLRLNISQTFYPIGALMGIVLGKYLVFQDGDSLHTQMAGMNAEQAHAFRLTMLEHTLE 202

Query: 211 PYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSLVSPLRH----PHVLFGVLAIFF 266
           PY  L +VL ++ +     R P    ++ + S+   SL    R+     H   G++A F 
Sbjct: 203 PYKYLVMVLVVVMLLFLFTRYPRCKPESSEKSLP--SLGETFRYLAGNRHFKRGIVAQFL 260

Query: 267 YVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRKLL 326
           YVG +VA+ SF +       +G  +E+ A+N++ Y ++   IG+F+ + L+ +    K+L
Sbjct: 261 YVGMQVAVWSFTIRLAL--TLGATNERHASNFMIYSFICFFIGKFVANFLMTRFRAEKVL 318

Query: 327 AIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERM-GPMTGEASSLL 385
            +++ + +  +   M      A+Y+ V + +     + TI++  +  +    T  A + +
Sbjct: 319 IVYSVLGVITLAWVMFVPNFTAVYAAVFVSVLFGPCWATIYAGTLATVDNKYTEVAGAFI 378

Query: 386 IMAIVGGAIVPFVQGLFADHIG-VQHAFFLPLLCYAYIVFY 425
           +M+IVG A +P +QG  +DH+G +Q AF + LLC+A++ FY
Sbjct: 379 VMSIVGAAFIPAIQGFVSDHLGSMQLAFGVSLLCFAWVGFY 419


Lambda     K      H
   0.327    0.140    0.414 

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: 462
Number of extensions: 28
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: 442
Length of database: 441
Length adjustment: 32
Effective length of query: 410
Effective length of database: 409
Effective search space:   167690
Effective search space used:   167690
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 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