GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gluP in Bacteroides fluxus YIT 12057

Align D-mannitol and D-mannose transporter (MFS superfamily) (characterized)
to candidate WP_009124055.1 HMPREF9446_RS03580 L-fucose:H+ symporter permease

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



>NCBI__GCF_000195635.1:WP_009124055.1
          Length = 439

 Score =  184 bits (466), Expect = 6e-51
 Identities = 135/413 (32%), Positives = 197/413 (47%), Gaps = 43/413 (10%)

Query: 25  FGAMTSLFFIWGFITALNDILIPHLKGIFDLSYTQAMLVQFCFFGAYFLVSPLAGVLIAR 84
           F  +TS F +WGF   + + ++     IF +S T   LVQ  F+G YF ++  A + I +
Sbjct: 21  FILITSCFALWGFANDITNPMVKAFSKIFRMSVTDGALVQVAFYGGYFAMAFPAAMFIRK 80

Query: 85  IGYLRGIIFGLSTMATGCLLFYPASSLEQYALFLLALFVLASGITILQVSANPFVARLGP 144
             Y  G++ GL   A G  LF+PA     Y  FL+A FVL  G++ L+ S+NP++  +G 
Sbjct: 81  YSYKAGVLLGLGLYALGAFLFFPAMLTGSYYPFLIAYFVLTCGLSFLETSSNPYILSMGT 140

Query: 145 ERTAASRLNLAQALNSLGHTLGPLFGSLLIFG------------AAAGTHEAVQ------ 186
           E TA  RLNLAQ+ N +G  LG       I               AA   EAV+      
Sbjct: 141 EETATRRLNLAQSFNPMGSLLGMYVAMNFIQNRLNPMDTVERSQLAAADFEAVRDSDLSV 200

Query: 187 --LPYLLLAAVIGIIAVGFIFLGGKVKHADMGVDHRHK-------GSLLSHKRLLLGALA 237
              PYL    VIGII +  +FL   VK      D  H+         +   K    G +A
Sbjct: 201 LIGPYL----VIGIIVLLMLFLIRMVK-MPKNADQSHEIDFFPTLKRIFRIKHYREGVIA 255

Query: 238 IFLYVGAEVSIGSFLVNYFAEPSIG-GLDEKSAAELVSWYWGGAMI----GRFAGAALTR 292
            F YVGA++   +F++ Y     +  G++EK+A  L   Y   AMI     RF    + R
Sbjct: 256 QFFYVGAQIMCWTFIIQYGTRLFMADGMEEKAAEVLSQEYNIIAMIIFCCSRFICTFILR 315

Query: 293 RFNPAMVLAANAVFANLLLMLTIVSSGELALVAVLAVGFFNSIMFPTIFTLAIEGLGELT 352
             +P ++L   A+ A LL    I       +  ++ V    S+MFPTI+ +A++GLG+  
Sbjct: 316 YLSPGLLLKVLAIVACLLTGGVIGFQNIWGMYCLVGVSACMSLMFPTIYGIALQGLGDDA 375

Query: 353 SRGSGLLCQAIVGGALLPVIQGVVADN------VGVQLSFIVPTFCYFYICWY 399
             G+  L  AI+GG++LP +Q  + D         V LSFI+P  C+  I  Y
Sbjct: 376 KFGAAGLIMAILGGSVLPPLQASIIDQHTLLGMPAVNLSFILPLICFVVITIY 428


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: 456
Number of extensions: 31
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: 413
Length of database: 439
Length adjustment: 32
Effective length of query: 381
Effective length of database: 407
Effective search space:   155067
Effective search space used:   155067
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