GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gluP in Megamonas funiformis YIT 11815

Align D-mannitol and D-mannose transporter (MFS superfamily) (characterized)
to candidate WP_008538694.1 HMPREF9454_RS06625 L-fucose:H+ symporter permease

Query= reanno::SB2B:6936374
         (413 letters)



>NCBI__GCF_000245775.1:WP_008538694.1
          Length = 438

 Score =  183 bits (464), Expect = 1e-50
 Identities = 123/418 (29%), Positives = 205/418 (49%), Gaps = 35/418 (8%)

Query: 25  FGAMTSLFFIWGFITALNDILIPHLKGIFDLSYTQAMLVQFCFFGAYFLVSPLAGVLIAR 84
           F  ++ LF +WG   +LNDILI   K +F LS   + LVQ  F+G YFL+S  A V+I +
Sbjct: 23  FVLLSCLFALWGAAASLNDILITQFKSVFTLSDFASALVQSAFYGGYFLISIPASVVIRK 82

Query: 85  IGYLRGIIFGLSTMATGCLLFYPASSLEQYALFLLALFVLASGITILQVSANPFVARLGP 144
             Y   I+ GL     GC LF+PAS +  Y +FL+A+F +A G+  L+ ++N +   LGP
Sbjct: 83  TTYKLAIMIGLIFYIGGCSLFFPASMMATYTMFLVAIFSIAIGLGFLETASNTYSTMLGP 142

Query: 145 ERTAASRLNLAQALNSLGHTLGPLFGSLLIF--------GAAAGTHEAVQL--------- 187
            + A  RLN++Q    +G   G L G  L+F          A  T + + L         
Sbjct: 143 RKYATLRLNISQTFQPIGSASGILLGKYLVFQEGESLASQMAQMTPDQIHLFRLQMLQHT 202

Query: 188 --PYLLLAAVIGIIAVGFIFLGGKVKHADMGVDHRHKGS-----------LLSHKRLLLG 234
             PY ++  +  ++A+  +FL  K     +     ++ +           L  +     G
Sbjct: 203 LEPYKIMICI--LVAIFILFLITKYPKCKVKEVANNQNTPKVTLGETLKYLSGNGLFKKG 260

Query: 235 ALAIFLYVGAEVSIGSFLVNYFAEPSIGGLDEKSAAELVSWYWGGAMIGRFAGAALTRRF 294
            +A FLYVG +V++ SF +   A   +  ++E+ AA+ +   +    +G+F    L  +F
Sbjct: 261 IVAQFLYVGMQVAVWSFTIR-LALDLMPHINERMAADFMVISFVCFFVGKFIANFLMTKF 319

Query: 295 NPAMVLAANAVFANLLLMLTIVSSGELALVAVLAVGFFNSIMFPTIFTLAIEGL-GELTS 353
           +   VL A ++   +L++         A+ A +A+       + TI+   ++ +  + T 
Sbjct: 320 SVNKVLLAYSIIGCILILYVAFIPNLTAIYAAVAISILLGPCWATIYAETLKSVEKKYTE 379

Query: 354 RGSGLLCQAIVGGALLPVIQGVVADNVG-VQLSFIVPTFCYFYICWYAFFARNRMNGE 410
               ++  +I+GGA +P +QG V+D VG +Q SFIV  FC+ YI WY ++     N E
Sbjct: 380 TAGAIIVMSIIGGAFMPAVQGFVSDMVGSMQFSFIVNFFCFAYIGWYFYYKMKLENKE 437


Lambda     K      H
   0.329    0.142    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: 388
Number of extensions: 16
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 413
Length of database: 438
Length adjustment: 32
Effective length of query: 381
Effective length of database: 406
Effective search space:   154686
Effective search space used:   154686
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 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