GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglB in Paraburkholderia bryophila 376MFSha3.1

Align glucose transporter, periplasmic substrate-binding component (characterized)
to candidate H281DRAFT_03877 H281DRAFT_03877 xylose-binding protein

Query= reanno::Phaeo:GFF3639
         (341 letters)



>FitnessBrowser__Burk376:H281DRAFT_03877
          Length = 342

 Score =  232 bits (592), Expect = 9e-66
 Identities = 131/325 (40%), Positives = 197/325 (60%), Gaps = 6/325 (1%)

Query: 7   VSALAFAATASMAFAEDVTVGVSWSNFQEERWKTDEAAIKAALEAKGATYVSADAQSSSA 66
           +++L+ AA  + A  +   +G    + + ERW  D     AA E  GA      A +S A
Sbjct: 19  LASLSLAAPLAHASKDHPEIGFCIDDLRVERWSRDRDYFVAAAEKLGAKVSVQSADASEA 78

Query: 67  KQLSDIESLIAQGVDALIVLAQDAQAIGPAVQAAADEGIPVVAYDRLIEDGRA-FYLTFD 125
           +Q+S IE+LI++GVD ++++  +++ +G  V  A   GI VV+YDRLI D     Y++FD
Sbjct: 79  RQISQIENLISRGVDVIVIVPFNSKTLGNVVAEARKAGIKVVSYDRLILDADVDAYISFD 138

Query: 126 NVEVGRMQARAVLEAQPSGNYVMIKGSPTDPNADFLRGGQQEIIQAAIDSGDIKIVGEAY 185
           N +VG +QA  V +AQP GNY ++ G+PTD NA  LR GQ ++++ AID GDIK+VG+ +
Sbjct: 139 NEKVGELQAEGVYKAQPKGNYFLLGGAPTDNNAKMLREGQLKVLKPAIDKGDIKLVGQQW 198

Query: 186 TDGWLPANAQRNMEQILTANDNKVDAVVASNDGTAGGVVAALTAQGMEG-IAVSGQDGDH 244
              W  + A R +E  LTAN+NK+DA+VASNDGTAGG + AL AQ M G + VSGQD D 
Sbjct: 199 VPEWSASTALRIVEDALTANNNKIDAIVASNDGTAGGAIQALAAQHMAGKVPVSGQDADL 258

Query: 245 AALNRVAKGTQTVSVWKDARDLGKAAANIAVEMAEGAVMGDVAGGAAWTSPAGTELTARF 304
           AA+ R+  GTQT++V+K  + +   AA ++V +A+    G+     A       ++    
Sbjct: 259 AAVKRLIAGTQTMTVYKPLKLIAGEAAKLSVALAK----GEKPAFNAQYDNGKKKVDTVL 314

Query: 305 LEPIPVTADNLSVVVDAGWITKEAL 329
           L+P  +T  N+ VV+  G+ T+  L
Sbjct: 315 LQPTLLTKSNVDVVIKDGFYTQAQL 339


Lambda     K      H
   0.313    0.128    0.362 

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: 225
Number of extensions: 8
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: 341
Length of database: 342
Length adjustment: 29
Effective length of query: 312
Effective length of database: 313
Effective search space:    97656
Effective search space used:    97656
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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