GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucP in Mucilaginibacter mallensis MP1X4

Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate WP_091372717.1 BLU33_RS11695 L-fucose:H+ symporter permease

Query= SwissProt::P11551
         (438 letters)



>NCBI__GCF_900105165.1:WP_091372717.1
          Length = 444

 Score =  327 bits (838), Expect = 5e-94
 Identities = 163/408 (39%), Positives = 245/408 (60%), Gaps = 4/408 (0%)

Query: 22  RSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIPIPA 81
           R  ++ F+L+  LF +W + NN+NDIL+ QF ++F L+  QAGLIQSAFY GYF + +P+
Sbjct: 17  RRNLLSFSLVTMLFLIWGIPNNMNDILIKQFMKSFELSRTQAGLIQSAFYMGYFFLAVPS 76

Query: 82  GILMKKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAANPF 141
           G++MKK SYK G+I GL L+ALG  LFWPAA    Y LFL  LF+IA+GL  LET AN F
Sbjct: 77  GLIMKKYSYKVGLIAGLLLFALGCCLFWPAAVAGKYGLFLFALFVIASGLTFLETGANIF 136

Query: 142 VTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLSAYK 201
           +  LG   S   RLN +Q FN  GA++ V+ G   ILS + H    +       +   Y 
Sbjct: 137 IVELGESQSAERRLNFSQAFNPIGAVLGVLIGTIFILSGIEHDPLKITAMKLSGEYQHYL 196

Query: 202 HSLVLSVQTPYMIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLARIRHWR 261
               + V TPY+++ A  +L ++ +M TKFP  + +     ++ +  A+   L +  H+ 
Sbjct: 197 QQETMRVVTPYLVLAAFAVLWSIFLMFTKFPKGRDEL---KEENAVKANSRELLKYPHFY 253

Query: 262 WAVLAQFCYVGAQTACWSYLIRYAVEEIPGMTAGFAANYLTGTMVCFFIGRFTGTWLISR 321
             V++QF Y GAQT  WS+ I+Y V++  G     A  +LTGT+V F +GRF+ T+++  
Sbjct: 254 KGVISQFFYCGAQTCTWSFFIQY-VQDFTGQPEKIAGYFLTGTLVAFGVGRFSATYIMRY 312

Query: 322 FAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNLGQDTK 381
            +P K++  Y  + + L  I+    G +G+ A+   S FMS+ YPT F+L I+NLG + K
Sbjct: 313 VSPGKLMGIYGFVNVGLVAIAILIPGFIGVWAIFFTSFFMSLMYPTNFALSIRNLGNNAK 372

Query: 382 YGSSFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVIFIFA 429
            G S +VM I+GG    PVMG ++++  ++  A +IP +C+  I  +A
Sbjct: 373 IGGSIMVMAIVGGAFFPPVMGLIAESTKSMAIAMVIPLICYLYIAYYA 420


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: 526
Number of extensions: 32
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: 438
Length of database: 444
Length adjustment: 32
Effective length of query: 406
Effective length of database: 412
Effective search space:   167272
Effective search space used:   167272
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