GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deoP in Dyella japonica UNC79MFTsu3.2

Align 2-Deoxy-D-ribose porter, DeoP (characterized)
to candidate N515DRAFT_1222 N515DRAFT_1222 MFS transporter, FHS family, L-fucose permease

Query= TCDB::Q8XEV7
         (438 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1222
          Length = 422

 Score =  253 bits (647), Expect = 6e-72
 Identities = 143/396 (36%), Positives = 221/396 (55%), Gaps = 4/396 (1%)

Query: 24  LLSCLFPLWGCAAALNDILITQFKSVFSLSNFASALVQSAFYGGYFLIAIPASLVIKKTS 83
           L+  LF LWG A  LND+LI QFK  F L++F + LVQSAFY GYFL+A+PA + +++  
Sbjct: 18  LIVSLFFLWGVANNLNDVLIPQFKKAFVLNDFQAGLVQSAFYLGYFLVAMPAGIYMRRFG 77

Query: 84  YKVAILIGLTLYIVGCTLFFPASHMATYTMFLAAIFAIAIGLSFLETAANTYSSMIGPKA 143
           YK A++ GL LY +G  LF+PA+   TY  FL A+F IA GL+FLET+AN + +++GP+ 
Sbjct: 78  YKSAVVFGLALYGLGALLFWPAAQQGTYGFFLFALFVIASGLAFLETSANPFVTLLGPRE 137

Query: 144 YATLRLNISQTFYPIGAAAGILLGKYLVFSEGESLEKQMAGMNAEQVHNFKVLMLENTLE 203
            A  RLN++Q F P+G+  GIL+G++ +FS  E   +Q+A ++A +   F          
Sbjct: 138 SAARRLNLAQAFNPLGSITGILIGQHFIFSGVEHTPEQLAALSAAERAAFVAHETAAVQL 197

Query: 204 PYKYMIMVLVVVMVLFLLTRFPTCKVAQTASHKRPSALDTLRYLASNARFRRGIVAQFLY 263
           PY  + +V++   +L LLTRFP     +  +  R      L  L  + RF   + AQF Y
Sbjct: 198 PYLAIGLVVLAWGLLILLTRFPAVHAVEEGAVPRDHG--ALARLLGDRRFLATLAAQFFY 255

Query: 264 VGMQVAVWSFTIR-LALELGDINERDASTFMVYSFACFFIGKFIANILMTRFNPEKVLIL 322
           VG QV VWS+ IR +   +     + A+ +M+ S ACF  G+F  + LM    P ++L L
Sbjct: 256 VGAQVGVWSYLIRYVQATMPGTPAKLAANYMLVSLACFMAGRFAGSALMRYVAPRRLLAL 315

Query: 323 YSVIGALFLAYVALAPSFSAVYVAVLVSVLFGPCWATIYAGTLDTVDNEHTEMAGAVIVM 382
           ++ +      +    P  +     V  S      + TI+A  ++   ++  ++  A++VM
Sbjct: 316 FAAVNVALTVFAVAVPGVAGACALVACSFFMSVMYPTIFALGVEGRGDDERKLGSALLVM 375

Query: 383 AIVGAAVVPAIQGYVADMFHSLQLSFLVSMLCFVYV 418
            I+G AV+ A  G V+D    +  + LV    FV +
Sbjct: 376 TIIGGAVLTAAMGAVSDA-AGISRAMLVPAASFVVI 410


Lambda     K      H
   0.329    0.139    0.412 

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: 404
Number of extensions: 24
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: 422
Length adjustment: 32
Effective length of query: 406
Effective length of database: 390
Effective search space:   158340
Effective search space used:   158340
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