GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucP in Shewanella loihica PV-4

Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate 5209419 Shew_1890 glucose/galactose transporter (RefSeq)

Query= SwissProt::P11551
         (438 letters)



>FitnessBrowser__PV4:5209419
          Length = 421

 Score =  239 bits (609), Expect = 2e-67
 Identities = 142/415 (34%), Positives = 223/415 (53%), Gaps = 20/415 (4%)

Query: 19  GQSRSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIP 78
           G+  +Y      L SLFF+W     LNDIL+P  + AF+L   +A LIQ  F+  YF++ 
Sbjct: 15  GEQENYRFALVSLTSLFFMWGFITCLNDILIPHLKAAFSLNYAEAMLIQFCFFGAYFLVS 74

Query: 79  IPAGILMKKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAA 138
           +PAG L+K L Y+ GI+TGL + ALG ALF+PAA +  Y LFL  LF++A+G+  L+ AA
Sbjct: 75  MPAGKLVKALGYQKGIVTGLLIAALGCALFYPAAALATYGLFLGALFVLASGITILQVAA 134

Query: 139 NPFVTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLS 198
           NP+V  LG   +   RLNL Q FN+ G  +A  FG  LILS     S+ +    +  ++ 
Sbjct: 135 NPYVNALGSVETASSRLNLTQAFNALGTTVAPYFGAVLILSVAVEASETLTQAQAEAEV- 193

Query: 199 AYKHSLVLSVQTPYMIIVAIVLLVALLIMLTKFPAL----QSDNHSDAKQGSFSASLSRL 254
                    V+ PY+I+   + ++AL+      P +    QS    +      +++L  L
Sbjct: 194 ---------VKLPYLILATALGVLALVFAKLDLPQIKEHCQSGEQGEVVHNGKTSALQSL 244

Query: 255 ARIRHWRWAVLAQFCYVGAQTACWSYLIRY-AVEEIPGMTAGFAANYLTGTMVCFFIGRF 313
               H     +  F YVGA+ +  S+L+ + A ++I G++   AA+Y+T       +GRF
Sbjct: 245 ----HLVLGAVGIFVYVGAEVSIGSFLVNFLAQDDIAGLSEASAASYITYYWGGAMVGRF 300

Query: 314 TGTWLISRFAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGI 373
            G+ ++ +     VL   AL+A  L  ++  + G V + A+     F SI +PTIFSL +
Sbjct: 301 IGSAVMQKVPAGTVLGFNALMAALLVALAMTSTGTVAMWAILAVGLFNSIMFPTIFSLAL 360

Query: 374 KNLGQDTKYGSSFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVIFIF 428
           ++LG  T  GS  + + I+GG I+  + G ++D  G I  A  +P +C+  I  +
Sbjct: 361 RDLGPHTSQGSGVLCLAIVGGAILPLLQGVLADNIG-IQHAFFLPIICYLFIMFY 414


Lambda     K      H
   0.329    0.140    0.425 

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: 456
Number of extensions: 30
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: 438
Length of database: 421
Length adjustment: 32
Effective length of query: 406
Effective length of database: 389
Effective search space:   157934
Effective search space used:   157934
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 (21.8 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