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_057508914.1 ABB28_RS12315 glucose/galactose MFS transporter

Query= uniprot:A0A1I2JXG1
         (442 letters)



>NCBI__GCF_001431535.1:WP_057508914.1
          Length = 438

 Score =  579 bits (1492), Expect = e-170
 Identities = 296/412 (71%), Positives = 343/412 (83%), Gaps = 1/412 (0%)

Query: 27  MAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLV 86
           MA+GV T+IFFMWGFLTCLNDILIPHLKAVF+LNYA AMLVQFTFFGAYFLMSLPAG LV
Sbjct: 24  MALGVATTIFFMWGFLTCLNDILIPHLKAVFELNYARAMLVQFTFFGAYFLMSLPAGRLV 83

Query: 87  ARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALL 146
           A LGYKKGIVAGL +AGVGA GFWPAA +  Y AFLGALFVLATGITVLQVAAN YVALL
Sbjct: 84  AHLGYKKGIVAGLLIAGVGALGFWPAAELREYSAFLGALFVLATGITVLQVAANPYVALL 143

Query: 147 GPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQEAQ 206
           GP +++SSRLTLAQALNSLGT +AP FGGLLIL   V SA++I  LS AEQ AYR  EAQ
Sbjct: 144 GPVETSSSRLTLAQALNSLGTAIAPIFGGLLILGNTVKSADEINALSVAEQAAYRAAEAQ 203

Query: 207 TVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQA-SVKQHSLVSPLRHPHVLFGVLAIF 265
           +VQGPY+GLAI L LLA+FVYLFRLP L+E  E+     Q S  + LRH H+LF VL IF
Sbjct: 204 SVQGPYIGLAIALVLLALFVYLFRLPTLSESAEKVDDGPQQSYGAALRHRHLLFAVLGIF 263

Query: 266 FYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRKL 325
           FYVG EV+IGSFLVNYLSMP IG  +EQ A ++V+ YW  AMIGRF GSALL + SPR +
Sbjct: 264 FYVGAEVSIGSFLVNYLSMPTIGGFTEQQATHYVSAYWTMAMIGRFAGSALLTRYSPRHM 323

Query: 326 LAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERMGPMTGEASSLL 385
           LA+FA IN+ L+ TTM + G VA+YSVV+IGLFNSIMFPTIF+LGIER+GP+T +ASSLL
Sbjct: 324 LALFAGINVLLLGTTMASSGQVALYSVVAIGLFNSIMFPTIFALGIERLGPLTNKASSLL 383

Query: 386 IMAIVGGAIVPFVQGLFADHIGVQHAFFLPLLCYAYIVFYGLYGSRIKSDTP 437
           IMAIVGGA+VP++QG+ ADHIG+Q +F LPLLCY Y++F+GL G+R+ +  P
Sbjct: 384 IMAIVGGALVPYLQGVLADHIGLQPSFILPLLCYGYVIFFGLVGARLPAIAP 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: 631
Number of extensions: 18
Number of successful extensions: 2
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