GapMind for catabolism of small carbon sources

 

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

Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate N515DRAFT_1222 N515DRAFT_1222 MFS transporter, FHS family, L-fucose permease

Query= SwissProt::P11551
         (438 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1222
          Length = 422

 Score =  379 bits (974), Expect = e-110
 Identities = 201/408 (49%), Positives = 266/408 (65%), Gaps = 5/408 (1%)

Query: 26  IPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIPIPAGILM 85
           +P AL+ SLFFLW VANNLND+L+PQF++AF L +FQAGL+QSAFY GYF++ +PAGI M
Sbjct: 14  LPLALIVSLFFLWGVANNLNDVLIPQFKKAFVLNDFQAGLVQSAFYLGYFLVAMPAGIYM 73

Query: 86  KKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAANPFVTVL 145
           ++  YK+ ++ GL LY LGA LFWPAA+   Y  FL  LF+IA+GL  LET+ANPFVT+L
Sbjct: 74  RRFGYKSAVVFGLALYGLGALLFWPAAQQGTYGFFLFALFVIASGLAFLETSANPFVTLL 133

Query: 146 GPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLSAYKHSLV 205
           GP  S   RLNLAQ FN  G+I  ++ GQ  I S V H + + L  +S  + +A+     
Sbjct: 134 GPRESAARRLNLAQAFNPLGSITGILIGQHFIFSGVEH-TPEQLAALSAAERAAFVAHET 192

Query: 206 LSVQTPYMIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLARIRHWRWAVL 265
            +VQ PY+ I  +VL   LLI+LT+FPA+ +       +     +L+RL   R +   + 
Sbjct: 193 AAVQLPYLAIGLVVLAWGLLILLTRFPAVHAVEEGAVPRD--HGALARLLGDRRFLATLA 250

Query: 266 AQFCYVGAQTACWSYLIRYAVEEIPGMTAGFAANYLTGTMVCFFIGRFTGTWLISRFAPH 325
           AQF YVGAQ   WSYLIRY    +PG  A  AANY+  ++ CF  GRF G+ L+   AP 
Sbjct: 251 AQFFYVGAQVGVWSYLIRYVQATMPGTPAKLAANYMLVSLACFMAGRFAGSALMRYVAPR 310

Query: 326 KVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNLGQD-TKYGS 384
           ++LA +A + +AL + +    G  G  AL  CS FMS+ YPTIF+LG++  G D  K GS
Sbjct: 311 RLLALFAAVNVALTVFAVAVPGVAGACALVACSFFMSVMYPTIFALGVEGRGDDERKLGS 370

Query: 385 SFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVIFIFARFR 432
           + +VMTIIGG ++T  MG VSDAAG I  A L+PA  F VI +FAR R
Sbjct: 371 ALLVMTIIGGAVLTAAMGAVSDAAG-ISRAMLVPAASFVVILLFARLR 417


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: 453
Number of extensions: 20
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