GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruP in Megamonas funiformis YIT 11815

Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate WP_008538694.1 HMPREF9454_RS06625 L-fucose:H+ symporter permease

Query= uniprot:A0A1I2JXG1
         (442 letters)



>NCBI__GCF_000245775.1:WP_008538694.1
          Length = 438

 Score =  205 bits (522), Expect = 2e-57
 Identities = 125/412 (30%), Positives = 228/412 (55%), Gaps = 9/412 (2%)

Query: 31  VLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLVARLG 90
           +L+ +F +WG    LNDILI   K+VF L+   + LVQ  F+G YFL+S+PA +++ +  
Sbjct: 25  LLSCLFALWGAAASLNDILITQFKSVFTLSDFASALVQSAFYGGYFLISIPASVVIRKTT 84

Query: 91  YKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALLGPEK 150
           YK  I+ GL     G + F+PA+ M  Y  FL A+F +A G+  L+ A+N Y  +LGP K
Sbjct: 85  YKLAIMIGLIFYIGGCSLFFPASMMATYTMFLVAIFSIAIGLGFLETASNTYSTMLGPRK 144

Query: 151 SASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQEAQTVQG 210
            A+ RL ++Q    +G+      G  L+       A Q+A+++P +   +R+Q  Q    
Sbjct: 145 YATLRLNISQTFQPIGSASGILLGKYLVFQEGESLASQMAQMTPDQIHLFRLQMLQHTLE 204

Query: 211 PYLGLAIVLFLLAVFVYLFRLP--ALTEKTEQASVKQHSLVSPLRH--PHVLF--GVLAI 264
           PY  +  +L  + +   + + P   + E     +  + +L   L++   + LF  G++A 
Sbjct: 205 PYKIMICILVAIFILFLITKYPKCKVKEVANNQNTPKVTLGETLKYLSGNGLFKKGIVAQ 264

Query: 265 FFYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRK 324
           F YVG +VA+ SF +  L++  + +++E+ AA+++   ++   +G+FI + L+ K S  K
Sbjct: 265 FLYVGMQVAVWSFTIR-LALDLMPHINERMAADFMVISFVCFFVGKFIANFLMTKFSVNK 323

Query: 325 LLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERM-GPMTGEASS 383
           +L  ++ I   L+L         A+Y+ V+I +     + TI++  ++ +    T  A +
Sbjct: 324 VLLAYSIIGCILILYVAFIPNLTAIYAAVAISILLGPCWATIYAETLKSVEKKYTETAGA 383

Query: 384 LLIMAIVGGAIVPFVQGLFADHIG-VQHAFFLPLLCYAYIVFYGLYGSRIKS 434
           +++M+I+GGA +P VQG  +D +G +Q +F +   C+AYI +Y  Y  ++++
Sbjct: 384 IIVMSIIGGAFMPAVQGFVSDMVGSMQFSFIVNFFCFAYIGWYFYYKMKLEN 435


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: 22
Number of successful extensions: 5
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: 438
Length adjustment: 32
Effective length of query: 410
Effective length of database: 406
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 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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