GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gluP in Bacteroides faecis MAJ27

Align D-mannitol and D-mannose transporter (MFS superfamily) (characterized)
to candidate WP_010538506.1 KCY_RS0118670 L-fucose:H+ symporter permease

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



>NCBI__GCF_000226135.1:WP_010538506.1
          Length = 438

 Score =  191 bits (484), Expect = 5e-53
 Identities = 136/419 (32%), Positives = 202/419 (48%), Gaps = 49/419 (11%)

Query: 25  FGAMTSLFFIWGFITALNDILIPHLKGIFDLSYTQAMLVQFCFFGAYFLVSPLAGVLIAR 84
           F  +TS F +WGF   + + ++     IF +S T   LVQ  F+G YF ++  A + I +
Sbjct: 20  FILITSCFALWGFANDITNPMVKAFSKIFRMSATDGALVQVAFYGGYFAMAFPAAMFIRK 79

Query: 85  IGYLRGIIFGLSTMATGCLLFYPASSLEQYALFLLALFVLASGITILQVSANPFVARLGP 144
             Y  G++ GL   A G  LF+PA    +Y  FL+A F+L  G++ L+ S NP++  +G 
Sbjct: 80  YSYKAGVLLGLGLYAFGAFLFFPAKMTGEYYPFLIAYFILTCGLSFLETSCNPYILSMGT 139

Query: 145 ERTAASRLNLAQALNSLGHTLGPLFGSLLIFGA---AAGTHEAVQL-------------- 187
           E TA  RLNLAQ+ N +G  LG +F ++    A     GT E   L              
Sbjct: 140 EETATRRLNLAQSFNPMGSLLG-MFVAMQFIQAKLHPMGTDERALLNESEFQAIKESDLA 198

Query: 188 ----PYLLLAAVIGIIAVGFIFLGGKVKHADMGVDHRHK-------GSLLSHKRLLLGAL 236
               PYL     IGI+ +  + L   VK    G D  HK         + +  R   G +
Sbjct: 199 VLIAPYL----TIGIVILAMLLLIRFVKMPKNG-DQNHKIDFFPTLKRIFTLTRYREGVI 253

Query: 237 AIFLYVGAEVSIGSFLVNY----FAEPSIGGLDEKSAAELVSWYWGGAM----IGRFAGA 288
           A F YVG ++   +F++ Y    F  P   G+DEKSA  L   Y   AM    I RF   
Sbjct: 254 AQFFYVGVQIMCWTFIIQYGTRLFMSPEY-GMDEKSAEVLSQQYNIIAMVIFCISRFICT 312

Query: 289 ALTRRFNPAMVLAANAVFANLLLMLTIVSSGELALVAVLAVGFFNSIMFPTIFTLAIEGL 348
            + R  N   +L   A+F  +  + TI       L  ++AV    S+MFPTI+ +A++G+
Sbjct: 313 FILRYLNAGKLLMILAIFGGIFTLGTIFLQNIFGLYCLVAVSACMSLMFPTIYGIALKGM 372

Query: 349 GELTSRGSGLLCQAIVGGALLPVIQGVVAD--NVG----VQLSFIVPTFCYFYICWYAF 401
           G+    G+  L  AI+GG++LP +Q  + D   +G    V +SFI+P  C+  I  Y +
Sbjct: 373 GDDAKFGAAGLIMAILGGSVLPPLQASIIDMKEIGSMPAVNVSFILPFICFLVIIGYGY 431


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: 466
Number of extensions: 26
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: 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