GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruP in Stenotrophomonas chelatiphaga DSM 21508

Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate WP_057509309.1 ABB28_RS14540 glucose/galactose MFS transporter

Query= uniprot:A0A1I2JXG1
         (442 letters)



>NCBI__GCF_001431535.1:WP_057509309.1
          Length = 429

 Score =  213 bits (543), Expect = 7e-60
 Identities = 136/415 (32%), Positives = 212/415 (51%), Gaps = 10/415 (2%)

Query: 23  TDYPMAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPA 82
           T    ++ ++  +FF+ GF T LN  LI  +K  F+L+   A LV   F+ +YF ++LP+
Sbjct: 11  TSVTTSIAIVGVLFFLIGFFTWLNGPLITFVKLAFELDEVGAFLVLMVFYLSYFFLALPS 70

Query: 83  GLLVARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAY 142
             ++ R G KKG+   L V   GAA F   A   +YP  LG LF++ +G+ +LQ A N Y
Sbjct: 71  SWILRRTGMKKGLSLSLLVMAAGAATFGEFATQRWYPGALGGLFIIGSGLALLQTAINPY 130

Query: 143 VALLGPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRV 202
           +++LGP ++A+ R+ L    N +   LAP   G L+L      +  + +   A + A   
Sbjct: 131 ISILGPIETAARRIALMGICNKVAGMLAPVLIGTLVLHGVGDLSTAVEQADVATRAALLN 190

Query: 203 QEAQTVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSLV---SPLRHPHVLF 259
             A  +  PYLG+A +L +L+V V    LP L      A+      +   S  + PH+  
Sbjct: 191 DFAAKIHAPYLGMAALLVVLSVAVLFSPLPELKSSEANAAPAGKGGIERSSIFQFPHLWL 250

Query: 260 GVLAIFFYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAM-IGRFIGSALLA 318
           GVL +F YVG EV  G  +  Y    D+     +   +      LGAM +G  +G  L+ 
Sbjct: 251 GVLCLFVYVGVEVMAGDAIGTYGHGFDLPLDQTKMFTSLT----LGAMLVGYVVGLLLIP 306

Query: 319 K-LSPRKLLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERMGPM 377
           + +S  + L+I A++ +   +    T G V++  V  +G  N++M+P IF L I  +G  
Sbjct: 307 RFVSQSRYLSISASLGVLFCVGAYFTHGYVSVAFVALLGFANAMMWPAIFPLAIRGLGRF 366

Query: 378 TGEASSLLIMAIVGGAIVPFVQGLFADHIGVQHAFFLPLL-CYAYIVFYGLYGSR 431
           T   S+LL+M I GGAI+P    +   H+  Q  F L ++ CY YI+FY   G R
Sbjct: 367 TETGSALLVMGIAGGAIIPQAFAVLKQHVDFQLVFLLLMVPCYLYILFYSTIGHR 421


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: 514
Number of extensions: 34
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: 429
Length adjustment: 32
Effective length of query: 410
Effective length of database: 397
Effective search space:   162770
Effective search space used:   162770
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