GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruP in Tatumella morbirosei LMG 23360

Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate WP_038017076.1 HA49_RS00365 L-fucose:H+ symporter permease

Query= uniprot:A0A1I2JXG1
         (442 letters)



>NCBI__GCF_000757425.2:WP_038017076.1
          Length = 408

 Score =  279 bits (714), Expect = 1e-79
 Identities = 162/419 (38%), Positives = 245/419 (58%), Gaps = 25/419 (5%)

Query: 9   PSKTSLPGAARERYTDYPMAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQ 68
           P    + GA   R+     A  ++T++FFMWG    L D+L  H +    +  A++ L+Q
Sbjct: 9   PDNAGVGGAVSLRW-----AFMLITTLFFMWGVSYGLLDVLNKHFQETLHVTKAQSGLLQ 63

Query: 69  FTFFGAYFLMSLPAGLLVARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVL 128
             +FGAYFL+++PAG  ++R GYK GI+AGLA+  +GA  F PAA ++ +  FL ALFVL
Sbjct: 64  GAYFGAYFLVAMPAGYFMSRHGYKAGILAGLALYAIGALLFVPAAMVNNFMMFLFALFVL 123

Query: 129 ATGITVLQVAANAYVALLGPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQ 188
           A G+  L+ AAN Y  +LG  + A  RL LAQ+ N LG F+ P  GG L  S A     Q
Sbjct: 124 ACGLGCLETAANPYATVLGDAQGAERRLNLAQSFNGLGQFMGPMIGGTLFFSHASADEAQ 183

Query: 189 IAKLSPAEQVAYRVQEAQTVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSL 248
                             TV+  Y+ +A V+  +A+      LP + E  E  S+  HS 
Sbjct: 184 -----------------STVKITYVVIACVVIGIALLFKRTALPDIREAEEAGSI--HSG 224

Query: 249 VSPLRHPHVLFGVLAIFFYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMI 308
            + L+H H + GV+A FFYV  +V +G+F +NY +    G ++ Q+AA  ++   +  M+
Sbjct: 225 QTLLQHKHFVGGVIAQFFYVAAQVGVGAFFINYTTEHWHG-VTNQSAAYMLSVGMVCFML 283

Query: 309 GRFIGSALLAKLSPRKLLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFS 368
           GRF  + L+ ++SP  +LA +A IN+ L    M+  G V++ ++V+I  F S MFPTIF+
Sbjct: 284 GRFFSTWLMGRVSPALILAAYALINIVLCAVVMLGMGDVSVIALVAIFFFMSTMFPTIFA 343

Query: 369 LGIERMGPMTGEASSLLIMAIVGGAIVPFVQGLFADHIGVQHAFFLPLLCYAYIVFYGL 427
           +G++ +GP T +ASS +IMAIVGGAI+P+  G  +D+     A+ LPL+C+A ++FY L
Sbjct: 344 MGVKNLGPATKQASSFMIMAIVGGAIMPWFMGRISDNSSTALAYGLPLVCFAVVLFYAL 402


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: 496
Number of extensions: 17
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: 442
Length of database: 408
Length adjustment: 32
Effective length of query: 410
Effective length of database: 376
Effective search space:   154160
Effective search space used:   154160
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