GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglB in Pseudomonas fluorescens FW300-N2C3

Align glucose transporter, periplasmic substrate-binding component (characterized)
to candidate AO356_28505 AO356_28505 sugar ABC transporter substrate-binding protein

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



>FitnessBrowser__pseudo5_N2C3_1:AO356_28505
          Length = 333

 Score =  226 bits (575), Expect = 8e-64
 Identities = 130/320 (40%), Positives = 187/320 (58%), Gaps = 6/320 (1%)

Query: 9   ALAFAATASMAFAEDVTVGVSWSNFQEERWKTDEAAIKAALEAKGATYVSADAQSSSAKQ 68
           ALA  +   MA A    +G S  + + ERW  D     AA E   A      A ++  KQ
Sbjct: 12  ALALLSLPVMADAAHPKIGFSIDDLRLERWSRDRDYFVAAAEKLDAKVFVQSADANEQKQ 71

Query: 69  LSDIESLIAQGVDALIVLAQDAQAIGPAVQAAADEGIPVVAYDRLIEDGRA-FYLTFDNV 127
           +S IE+LI++GVD ++++  +A  +  AV  A   GI VV+YDRLI +     Y++FDN 
Sbjct: 72  ISQIENLISRGVDVIVIVPFNATVLTNAVAEAKKAGIKVVSYDRLILNADIDAYISFDNE 131

Query: 128 EVGRMQARAVLEAQPSGNYVMIKGSPTDPNADFLRGGQQEIIQAAIDSGDIKIVGEAYTD 187
           +VG MQA  VL+A P GNY ++ G+PTD NA  LR GQ +++Q AID GDIKIVG+ +  
Sbjct: 132 KVGEMQASGVLKAAPKGNYFLLGGAPTDNNAKVLREGQMKVLQPAIDKGDIKIVGQQWVK 191

Query: 188 GWLPANAQRNMEQILTANDNKVDAVVASNDGTAGGVVAALTAQGMEG-IAVSGQDGDHAA 246
            W P  A   +E  LT N+NK+D +VASND TAGG + AL AQ M G + +SGQD D AA
Sbjct: 192 EWNPTEALSIVENALTRNNNKIDGIVASNDATAGGAIQALAAQKMAGKVPISGQDADLAA 251

Query: 247 LNRVAKGTQTVSVWKDARDLGKAAANIAVEMAEGAVMGDVAGGAAWTSPAGTELTARFLE 306
           + RV  GTQT++V+K  + +   AA ++V++A      +    ++       ++    L 
Sbjct: 252 VKRVIDGTQTMTVYKPLKLIASEAAKLSVQLAR----NEKPTFSSQYDNGSKKVDTILLT 307

Query: 307 PIPVTADNLSVVVDAGWITK 326
           P P+T DN+ ++   G+ TK
Sbjct: 308 PTPLTKDNIDLLEKDGFYTK 327


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: 209
Number of extensions: 7
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: 333
Length adjustment: 28
Effective length of query: 313
Effective length of database: 305
Effective search space:    95465
Effective search space used:    95465
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