GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01115 in Paraburkholderia bryophila 376MFSha3.1

Align deoxynucleoside transporter, permease component 1 (characterized)
to candidate H281DRAFT_02176 H281DRAFT_02176 monosaccharide ABC transporter membrane protein, CUT2 family

Query= reanno::Burk376:H281DRAFT_01115
         (357 letters)



>FitnessBrowser__Burk376:H281DRAFT_02176
          Length = 321

 Score =  105 bits (261), Expect = 2e-27
 Identities = 95/307 (30%), Positives = 146/307 (47%), Gaps = 21/307 (6%)

Query: 19  LLIVNVLVVLVATWLSRGQ-FVDIDNLQSMGGQLPELGLLALGIMLSMVSGNGGIDLSGV 77
           L I+  LV LV   L R + F    N+ S         L+++G+   +++G  GIDLS  
Sbjct: 5   LPILLALVALVVLGLVRYEHFASAYNITSFWRYNSMFALISVGMAFVIITG--GIDLSVG 62

Query: 78  GLANLSGMVAAMLVPRLVNGDDSPVLYTSLFCAIVLMMGLLGGLLNGVVIARLRLTPILC 137
            +A +S +VAA+      +G    V+     CA     GL  G+LNGV+I RL++ P + 
Sbjct: 63  TVAAMSSVVAALAS---AHGGWVAVVAG---CAA----GLAVGVLNGVIITRLKILPFIV 112

Query: 138 TLGTQLLFTGFAVVISNGASVHVDYVEPLSDIGNGTVLQVPIAFCIFLAAVIVLGWLLKR 197
           TL T L   G A+++    +V +      ++ G G +  +PI   I  A V V GWL  R
Sbjct: 113 TLATSLGAHGVALLLGKNDAVSIASDSNFANFGQGDLFGLPIP-GIVAALVAVAGWLALR 171

Query: 198 SP-FGLRLYLMGTNPKAAFYAGIPRARMLITTYAMCGVLASLAGLISATHTSSAKWDYGN 256
           S  FG     +G + +AA   G+   R L+  YA+ G+LA +AG+I A    + + + G 
Sbjct: 172 STRFGRHSLAIGGSEEAARLMGLNVDRTLVMAYAVSGLLAGMAGVILAAQFGAGQPNEGV 231

Query: 257 SYLLIAILIAVMGGVNPAGGHGRIICVFFAATVLQFLSSLFN------LLGVSQFFGDCA 310
            + L AI   V+GG    GG G I        +L  + +L N       + +S ++    
Sbjct: 232 GWELFAISAVVLGGTLLTGGEGSIAMTIAGVLLLGLVFNLLNFENGLGFISLSAYWQSVI 291

Query: 311 WGFLLLL 317
            G  LLL
Sbjct: 292 RGVFLLL 298


Lambda     K      H
   0.327    0.143    0.429 

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: 316
Number of extensions: 18
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: 357
Length of database: 321
Length adjustment: 28
Effective length of query: 329
Effective length of database: 293
Effective search space:    96397
Effective search space used:    96397
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 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