GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Dyella japonica UNC79MFTsu3.2

Align L-iditol 2-dehydrogenase (EC 1.1.1.14); D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate N515DRAFT_0211 N515DRAFT_0211 Threonine dehydrogenase

Query= reanno::HerbieS:HSERO_RS17015
         (345 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0211
          Length = 338

 Score = 85.5 bits (210), Expect = 2e-21
 Identities = 93/333 (27%), Positives = 129/333 (38%), Gaps = 15/333 (4%)

Query: 1   MQALVLEATRELKLREIDLPQQMGAQDVRIRIHTVGICGSDLHYYTHGSIGPFKVEAPMV 60
           M+  VL    +++  E+  P+     D  IRI    +CGSDL  Y   S G      P  
Sbjct: 1   MKGTVLHGPNDIRFEEVPEPKIEKPTDAIIRIAVTCVCGSDLWPYRGISPG----SGPTR 56

Query: 61  LGHEASGTVIEVGSAVSHLKVGDRVCMEPGIPRLDSPATLRGMYNLDPAVRFWATPPIHG 120
           +GHE  G V EVGSAV  +K G  V           P    G Y      R + +     
Sbjct: 57  MGHEYCGYVEEVGSAVMAIKKGQFVVGSFATSDNTCPTCNIG-YQSSCVQREFVSQAQSP 115

Query: 121 CLTGSVVHPAAFTYRLPDNVSFAEGAIV--EPLSIGLQAATKARMKPGDTAVVIGAGTIG 178
            L  +         R   + S   G +   + L  G  AA  AR++PG TAVV+G G +G
Sbjct: 116 YLRVAHADGTLVATREAPDASMVPGLLASSDVLGTGWYAADAARVRPGVTAVVVGDGAVG 175

Query: 179 AMTALAALAGGAARVILADVVAEKLAHFADNPAVITVDVTRETLTDVVRQATDGWGADVV 238
            +  L+A   GA R+I+      +     D  A   V    E     + + T G GAD V
Sbjct: 176 LLAVLSAKQMGAERIIVMSRHPARQKLALDFGATDIVAERGEEGVARIMELTRGLGADSV 235

Query: 239 FEASGHAGVYQTLLDLVCPGGCAVLVGMPPAPVALDVVAMQTKEVRLES----VFRYANI 294
            E  G     Q  + +   GG    VG+P   V ++  A+    + LE     V RY   
Sbjct: 236 LECVGTGESMQQAMRVTRKGGHMSFVGVPHG-VEIEGQALFFSHIHLEGGPAPVRRY--- 291

Query: 295 FPRALALISSGMIDVKPFISRKFPFSQSIRAFE 327
            P  + LI    ID         P  Q    ++
Sbjct: 292 LPDLIDLILDQKIDPSAVFDLVLPLDQVAEGYK 324


Lambda     K      H
   0.321    0.137    0.403 

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: 268
Number of extensions: 17
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 345
Length of database: 338
Length adjustment: 29
Effective length of query: 316
Effective length of database: 309
Effective search space:    97644
Effective search space used:    97644
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 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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