GapMind for catabolism of small carbon sources

 

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

Align Inner-membrane translocator (characterized, see rationale)
to candidate H281DRAFT_05271 H281DRAFT_05271 monosaccharide ABC transporter membrane protein, CUT2 family

Query= uniprot:A0KWY6
         (405 letters)



>FitnessBrowser__Burk376:H281DRAFT_05271
          Length = 347

 Score =  291 bits (746), Expect = 2e-83
 Identities = 153/313 (48%), Positives = 218/313 (69%), Gaps = 4/313 (1%)

Query: 63  LWPLLALSILLLANLFIDSSFFNISYQDDRLYGSLIDILNRSAPVALLSIGMSLVIATGG 122
           +WP + L++L   NL+++  F ++   D  L+G+ ID+LNR+AP+ L++ GM+LVIAT G
Sbjct: 17  IWPCVTLALLCALNLWVNPHFLSLRMLDGHLFGAPIDVLNRAAPLVLVATGMTLVIATRG 76

Query: 123 IDLSVGAVMAIAGAVCANLLLVPDISLVTVIA----AGLIVGLLAGCINGGLVSFLGIQP 178
           ID+SVGAV+AIAGA  A +L    +    +IA    A LIVG+L+G  NG LVSF+G+QP
Sbjct: 77  IDISVGAVVAIAGAAAATILATQPVPTGNLIAQALLAALIVGVLSGMWNGLLVSFVGMQP 136

Query: 179 IVATLLLMVAGRGVAQLINQGQIITFQHPGFAAIGVGQFLGLPMPVWIVIGMLTFSQLLL 238
           I+ATL+LMVAGRG+AQL+  GQII    PG+  +G G +LG+P  VWI    +  +  L+
Sbjct: 137 IIATLILMVAGRGIAQLLTAGQIIPIGAPGYLFVGGGYWLGVPCSVWIATIAVLATAALV 196

Query: 239 RKTALGLFIEAVGCNAKASRYLGINDKSIKLFAYGIAGLCAALAGMISTADIQGSDANNA 298
             TALGLFI A+G N  A+R +G+  K++    YG +GL AA+AG++ +++++ +D NNA
Sbjct: 197 EGTALGLFIRAIGVNPVATRLVGLRSKALVFAVYGFSGLTAAMAGILISSNVRSADGNNA 256

Query: 299 GLWLELDAVLAVVIGGAALTGGRFSLILSVVGALIIQTLATTIIVSGLPAKFNLLIKAIV 358
           GL LELDA+LAV +GG +L GGRFS   +V+GALIIQTL  T    G+P +  L++KA V
Sbjct: 257 GLLLELDAILAVTLGGTSLLGGRFSFAGTVLGALIIQTLTYTTYSIGVPPEATLVVKAAV 316

Query: 359 ILTVLLLQSAKFR 371
           +LTV ++QS   R
Sbjct: 317 VLTVSVIQSPAAR 329


Lambda     K      H
   0.323    0.136    0.379 

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: 357
Number of extensions: 17
Number of successful extensions: 2
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: 405
Length of database: 347
Length adjustment: 30
Effective length of query: 375
Effective length of database: 317
Effective search space:   118875
Effective search space used:   118875
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 bits)
S2: 50 (23.9 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