GapMind for catabolism of small carbon sources

 

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

Align D-mannitol and D-mannose transporter (MFS superfamily) (characterized)
to candidate N515DRAFT_1222 N515DRAFT_1222 MFS transporter, FHS family, L-fucose permease

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



>FitnessBrowser__Dyella79:N515DRAFT_1222
          Length = 422

 Score =  249 bits (635), Expect = 1e-70
 Identities = 159/414 (38%), Positives = 213/414 (51%), Gaps = 29/414 (7%)

Query: 13  SAAPAQSHQQLLFGAMTSLFFIWGFITALNDILIPHLKGIFDLSYTQAMLVQFCFFGAYF 72
           S++ A     L    + SLFF+WG    LND+LIP  K  F L+  QA LVQ  F+  YF
Sbjct: 4   SSSRAAGRSPLPLALIVSLFFLWGVANNLNDVLIPQFKKAFVLNDFQAGLVQSAFYLGYF 63

Query: 73  LVSPLAGVLIARIGYLRGIIFGLSTMATGCLLFYPASSLEQYALFLLALFVLASGITILQ 132
           LV+  AG+ + R GY   ++FGL+    G LLF+PA+    Y  FL ALFV+ASG+  L+
Sbjct: 64  LVAMPAGIYMRRFGYKSAVVFGLALYGLGALLFWPAAQQGTYGFFLFALFVIASGLAFLE 123

Query: 133 VSANPFVARLGPERTAASRLNLAQALNSLGHTLGPLFGSLLIFGAAAGTHE--------- 183
            SANPFV  LGP  +AA RLNLAQA N LG   G L G   IF     T E         
Sbjct: 124 TSANPFVTLLGPRESAARRLNLAQAFNPLGSITGILIGQHFIFSGVEHTPEQLAALSAAE 183

Query: 184 ----------AVQLPYLLLAAVIGIIAVGFIFLGGK------VKHADMGVDHRHKGSLLS 227
                     AVQLPYL +  V  ++A G + L  +      V+   +  DH     LL 
Sbjct: 184 RAAFVAHETAAVQLPYLAIGLV--VLAWGLLILLTRFPAVHAVEEGAVPRDHGALARLLG 241

Query: 228 HKRLLLGALAIFLYVGAEVSIGSFLVNYFAEPSIGGLDEKSAAELVSWYWGGAMIGRFAG 287
            +R L    A F YVGA+V + S+L+ Y  + ++ G   K AA  +       M GRFAG
Sbjct: 242 DRRFLATLAAQFFYVGAQVGVWSYLIRY-VQATMPGTPAKLAANYMLVSLACFMAGRFAG 300

Query: 288 AALTRRFNPAMVLAANAVFANLLLMLTIVSSGELALVAVLAVGFFNSIMFPTIFTLAIEG 347
           +AL R   P  +LA  A     L +  +   G     A++A  FF S+M+PTIF L +EG
Sbjct: 301 SALMRYVAPRRLLALFAAVNVALTVFAVAVPGVAGACALVACSFFMSVMYPTIFALGVEG 360

Query: 348 LGELTSR-GSGLLCQAIVGGALLPVIQGVVADNVGVQLSFIVPTFCYFYICWYA 400
            G+   + GS LL   I+GGA+L    G V+D  G+  + +VP   +  I  +A
Sbjct: 361 RGDDERKLGSALLVMTIIGGAVLTAAMGAVSDAAGISRAMLVPAASFVVILLFA 414


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: 486
Number of extensions: 19
Number of successful extensions: 5
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: 422
Length adjustment: 32
Effective length of query: 381
Effective length of database: 390
Effective search space:   148590
Effective search space used:   148590
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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