GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglB in Collimonas pratensis Ter91

Align glucose transporter, periplasmic substrate-binding component (characterized)
to candidate WP_061938410.1 CPter91_RS06285 D-xylose ABC transporter substrate-binding protein

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



>NCBI__GCF_001584185.1:WP_061938410.1
          Length = 338

 Score =  229 bits (584), Expect = 8e-65
 Identities = 127/325 (39%), Positives = 196/325 (60%), Gaps = 6/325 (1%)

Query: 4   LSGVSALAFAATASMAFAEDVTVGVSWSNFQEERWKTDEAAIKAALEAKGATYVSADAQS 63
           +  V+  +  ++A+MA A++  +G S  + + ERW  D     AA +  GA      A +
Sbjct: 12  MMSVAVFSLTSSAAMADAKNPKIGFSIDDLRVERWARDRDFFIAAADKLGAKVFVQSADA 71

Query: 64  SSAKQLSDIESLIAQGVDALIVLAQDAQAIGPAVQAAADEGIPVVAYDRLIEDGRA-FYL 122
           S  +Q+S IE+LI++GVD ++++  +A  +   ++ A   GI VV+YDRLI +     Y+
Sbjct: 72  SEQRQISQIENLISRGVDVIVIVPFNATVLSNTIKEAKKAGIKVVSYDRLILNADIDAYI 131

Query: 123 TFDNVEVGRMQARAVLEAQPSGNYVMIKGSPTDPNADFLRGGQQEIIQAAIDSGDIKIVG 182
           +FDN +VG MQA  VL+AQP GNY ++ GSPTD NA  LR GQ +++Q +ID GDIKIVG
Sbjct: 132 SFDNEKVGEMQAEGVLKAQPKGNYYLLGGSPTDNNAKMLREGQMKVLQPSIDKGDIKIVG 191

Query: 183 EAYTDGWLPANAQRNMEQILTANDNKVDAVVASNDGTAGGVVAALTAQGMEG-IAVSGQD 241
           + +   W    A   +E  LTAN+NK+DA+VASNDGTAGG + AL +Q M G + VSGQD
Sbjct: 192 QQWVKDWSATEALSIVENALTANNNKIDAIVASNDGTAGGAIQALASQKMAGKVPVSGQD 251

Query: 242 GDHAALNRVAKGTQTVSVWKDARDLGKAAANIAVEMAEGAVMGDVAGGAAWTSPAGTELT 301
            D AA+ RV  GTQ+++V+K  + +   AA ++V++A      +     +       ++ 
Sbjct: 252 ADLAAVKRVIAGTQSMTVYKPLKLIASEAAKLSVQLAR----NEKPSYNSQYENGAKKVD 307

Query: 302 ARFLEPIPVTADNLSVVVDAGWITK 326
              L+P  +T  N+ ++V  G+ T+
Sbjct: 308 TILLKPTTLTKANVDLLVTDGFYTQ 332


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: 215
Number of extensions: 8
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: 341
Length of database: 338
Length adjustment: 28
Effective length of query: 313
Effective length of database: 310
Effective search space:    97030
Effective search space used:    97030
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 24 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