GapMind for catabolism of small carbon sources

 

Aligments for a candidate for MFS-glucose in Dyella japonica UNC79MFTsu3.2

Align Glucose/galactose transporter (characterized, see rationale)
to candidate N515DRAFT_1918 N515DRAFT_1918 MFS transporter, FHS family, L-fucose permease

Query= uniprot:A0KXM0
         (423 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1918
          Length = 442

 Score =  427 bits (1097), Expect = e-124
 Identities = 222/412 (53%), Positives = 294/412 (71%), Gaps = 12/412 (2%)

Query: 21  NYRFALVSLTSLFFMWGFITCLNDILIPHLKAVFSLNYTQAMLIQFCFFGAYFLVSIPAG 80
           +Y  A+  LTS+FFMWGF+TCLNDILIPHLKAVF LNY +AML+QF FFGAYFL+S+PAG
Sbjct: 24  DYPMAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAG 83

Query: 81  QLVKRLGYQKGIVTGLVIASIGCGLFYPAASFATYGLFLGALFVLASGITILQVAANPYV 140
            LV RLGY+KGIV GL +A +G   F+PAA+   Y  FLGALFVLA+GIT+LQVAAN YV
Sbjct: 84  LLVARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYV 143

Query: 141 NALGSSETASSRLNLTQAFNALGTTVAPFFGSILILSVAASVSSELAQAN---------A 191
             LG  ++ASSRL L QA N+LGT +AP FG +LILS A   + ++A+ +          
Sbjct: 144 ALLGPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQ 203

Query: 192 EAEVVKLPYLLLAAALAVLAIIFAKLDLPVIREHSQAAAEEVQTHLGKTSALQSMHLVLG 251
           EA+ V+ PYL LA  L +LA+      LP + E ++ A+  V+ H    S L+  H++ G
Sbjct: 204 EAQTVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQAS--VKQH-SLVSPLRHPHVLFG 260

Query: 252 AVGIFVYVGAEVSIGSFLVNFLGEAHIVGMPEEQAAHYIAYYWGGAMVGRFIGSAVMQKI 311
            + IF YVG EV+IGSFLVN+L    I  M E+ AA+++AYYW GAM+GRFIGSA++ K+
Sbjct: 261 VLAIFFYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKL 320

Query: 312 PAGTVLAFNAFMAALLVLVAMTTSGSVAMWAILGVGLFNSIMFPTIFSLALRDLGPHTSQ 371
               +LA  A +   LVL  M T G+VAM++++ +GLFNSIMFPTIFSL +  +GP T +
Sbjct: 321 SPRKLLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERMGPMTGE 380

Query: 372 GSGILCLAIVGGAIVPLLQGVLADNLGIQLAFILPVVCYGFILFYGAKGSKM 423
            S +L +AIVGGAIVP +QG+ AD++G+Q AF LP++CY +I+FYG  GS++
Sbjct: 381 ASSLLIMAIVGGAIVPFVQGLFADHIGVQHAFFLPLLCYAYIVFYGLYGSRI 432


Lambda     K      H
   0.326    0.138    0.402 

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: 576
Number of extensions: 25
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: 423
Length of database: 442
Length adjustment: 32
Effective length of query: 391
Effective length of database: 410
Effective search space:   160310
Effective search space used:   160310
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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