GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Dyella japonica UNC79MFTsu3.2

Align Inositol transport system permease protein (characterized)
to candidate N515DRAFT_2415 N515DRAFT_2415 simple sugar transport system permease protein

Query= reanno::WCS417:GFF2333
         (340 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2415
          Length = 337

 Score =  137 bits (345), Expect = 4e-37
 Identities = 107/359 (29%), Positives = 184/359 (51%), Gaps = 43/359 (11%)

Query: 1   MNAITDNKPATVPTKSRRR----------LPTELSIFLVLIGIGLVFELFGWIVRDQSFL 50
           MNA+    PA     + RR          L   L +F+ + G G V  L+   +  Q FL
Sbjct: 1   MNAVA---PAATSAAAGRRPWWRRRAQVPLLVTLVLFVAMAGAGGV--LYHGFLTPQVFL 55

Query: 51  MNSQRLVLMILQVSIIGLLAIGVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFSRAV 110
                   +++  + + ++A+G+T VI+  GIDLS G+V+A S ++ A L Q     R  
Sbjct: 56  N-------LLIDNAFLCIVAVGMTFVILAGGIDLSVGAVVAFSTVLLAELVQ-----RHG 103

Query: 111 FPSLTDLPVWIPVAMGLGVGLLAGAINGSIIAVTGIPPFIATLGMMVSARGLARYYTEG- 169
           +P L  + + + V  G G G+      G +I    + PF+ TL  M  ARG+A   +   
Sbjct: 104 WPPLAAIALVLAVGTGFGAGM------GVLIQRFRLQPFVVTLAGMFLARGVATLISVDS 157

Query: 170 ----QP-VSMLSDSYTAIGHGAM---PVIIFLVVAVIFHIALRYTKYGKYTYAIGGNMQA 221
               QP ++ +++    +G G+M     ++ L V     +    + +G+  YAIGG+  +
Sbjct: 158 IDIDQPWLASVANLRLPLGGGSMLSVGALVALAVVAAGALLAGASSFGRTVYAIGGSESS 217

Query: 222 ARTSGINVKRHLIIVYSIAGLLAGLAGVVASARAATGQAGMGMSYELDAIAAAVIGGTSL 281
           AR  G+ V   ++ VY+++G  A LAGVV +    +G +   +  ELDAIAA VIGGT L
Sbjct: 218 ARLMGLPVDATVVRVYALSGFCAALAGVVYTLYMLSGYSQHALGLELDAIAAVVIGGTVL 277

Query: 282 AGGVGRITGTVIGALILGVMASGFTFVG-VDAYIQDIIKGLIIVVAVVIDQYRNKRKLK 339
           AGG G + GT++G L+LG++ +   F G + ++   I+ G +++   ++ +   ++++K
Sbjct: 278 AGGSGYVLGTLLGVLVLGLIQTLIVFDGELSSWWTRIVIGALLLAFCLLQRLFRRKEIK 336


Lambda     K      H
   0.325    0.140    0.394 

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: 277
Number of extensions: 19
Number of successful extensions: 3
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: 340
Length of database: 337
Length adjustment: 28
Effective length of query: 312
Effective length of database: 309
Effective search space:    96408
Effective search space used:    96408
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 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