GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruP in Dyella japonica UNC79MFTsu3.2

Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate N515DRAFT_0592 N515DRAFT_0592 glucose/galactose transporter

Query= uniprot:A0A1I2JXG1
         (442 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0592
          Length = 430

 Score =  221 bits (563), Expect = 3e-62
 Identities = 144/416 (34%), Positives = 217/416 (52%), Gaps = 13/416 (3%)

Query: 29  MGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLVAR 88
           M ++  +FF++GF+T LN  LI  +K  F L+   A LV   F+ +YF ++LP+  ++ R
Sbjct: 21  MLIIGLLFFIFGFVTWLNGPLITFVKLAFSLDDVNAFLVPMVFYCSYFFLALPSSAVLKR 80

Query: 89  LGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALLGP 148
            G KKG+  GL V  +GA  F    +M  Y   L  LFV+  G+ +LQ A+N Y+++LGP
Sbjct: 81  TGMKKGMALGLFVMAIGAVLFGQFVSMRVYGGALAGLFVIGAGLALLQTASNPYISILGP 140

Query: 149 EKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQI-AKLSPAEQVAYRVQEAQT 207
             SA+ R+      N +   LAP   G L+LS      +Q+ A  +P  + A     A  
Sbjct: 141 IDSAAQRIAFMGICNKVAGALAPFVFGWLVLSGIDTFDQQVKAAPTPEAREALLNTFAAK 200

Query: 208 VQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVK-QHSLVSPLRHPHVLFGVLAIFF 266
           V  PYL +A +L LLAV+V    LP +      +  +  H+  + L  PH+  GVL +F 
Sbjct: 201 VHMPYLAMAGLLVLLAVWVLRSPLPEIKPSGANSEAEIGHAKGNLLSFPHLWLGVLCLFL 260

Query: 267 YVGGEVAIGSFLVNY---LSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAK-LSP 322
           YVG EV  G  +  Y   L +P        A  ++ ++     ++G   G  L+ K +S 
Sbjct: 261 YVGVEVMAGDAIGTYGQGLGLP------LDATKHFTSFTLFAMLLGYLAGLVLIPKIISQ 314

Query: 323 RKLLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERMGPMTGEAS 382
           +  LA+ A + +A  +    T G  ++  V ++G  N++M+P IF L I+ +G  T   S
Sbjct: 315 QSYLAVSAVLGVAFTVGAWATTGYTSVGFVAALGFANAMMWPAIFPLAIKGLGRWTEAGS 374

Query: 383 SLLIMAIVGGAIVPFVQGLFADHIGVQHAFFLPLL-CYAYIVFYGLYGSRIKSDTP 437
           +LLIMAIVGGA+VP        H   Q  F L ++ CY YI+FYGL G R+    P
Sbjct: 375 ALLIMAIVGGALVPQAFVHLKQHYDFQLVFMLLMVPCYLYILFYGLRGHRVGQHAP 430


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: 29
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: 430
Length adjustment: 32
Effective length of query: 410
Effective length of database: 398
Effective search space:   163180
Effective search space used:   163180
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 17 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