GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Klebsiella michiganensis M5al

Align D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate BWI76_RS24895 BWI76_RS24895 galactitol-1-phosphate 5-dehydrogenase

Query= BRENDA::Q86ZV0
         (358 letters)



>FitnessBrowser__Koxy:BWI76_RS24895
          Length = 347

 Score =  159 bits (403), Expect = 8e-44
 Identities = 109/353 (30%), Positives = 175/353 (49%), Gaps = 36/353 (10%)

Query: 12  SFVLEGIHKVKFEDRPIPQLRDAHDVLVDVRFTGICGSDV--------HYWEHGSIGQFV 63
           S V+     V+ E+RPIP L+  +DVLV V  +G+CGSD+        HY+         
Sbjct: 3   SVVIHAEGTVRVEERPIPTLQTENDVLVKVVSSGLCGSDIPRIFAKGAHYY--------- 53

Query: 64  VKDPMVLGHESSGVISKVGSAVTTLKVGDHVAMEPGIPCRRCEPCKEGKYNLCEKMAFAA 123
              P+ LGHE SG +   GSAVT L+ GD VA  P +PC  C  C+   ++LC++  F  
Sbjct: 54  ---PITLGHEFSGYVESYGSAVTDLQPGDAVACVPLLPCFNCPQCQREYFSLCKQYQFVG 110

Query: 124 TPPYDGTLAKYYVLPEDFCYKLPENINLQEAAVMEPLSVAVHIVKQANVAPGQSVVVFGA 183
           +    G  A+Y V+     ++LP+ + + + A +EP++V +H    A    G++V++ GA
Sbjct: 111 SRSEGGN-AEYVVVKRANLFRLPDRMPIDDGAFIEPMTVGLHAFHLAQGCEGKNVIIIGA 169

Query: 184 GPVGLLCCAVARAFGSPKVIAVDIQKGRLEFAKKYAATAIFEPSKVSALENAERIVNEND 243
           G +GLL    AR  G+  + A+DI   RL  AK   AT +F   ++S+ E  +  + E  
Sbjct: 170 GTIGLLALQCARELGAKSITAIDINPQRLALAKTLGATYVFNSKEMSSKE-IQTALEEIQ 228

Query: 244 LGRGADIVIDASGAEPSVHTGIHVLRPGGTYVQGGMGRNEITF---PIMAACTKELNVRG 300
             +   +V++ +G   +V  GI V  P       G   +++T           KEL + G
Sbjct: 229 FDQ---LVLETAGTPQTVALGIEVAGPRAQLALVGTLHHDLTLLSATFGQILRKELTIVG 285

Query: 301 SFRYGSG-----DYKLAVNLVASGKVSVKELITGVVSFEDAEQAFHEVKAGKG 348
           S+   SG     +++ AV L+   ++ +  LI  +    +AE    EV+A  G
Sbjct: 286 SWMNYSGPWPGEEWQTAVRLLTEKRIQLVPLIAHI---GNAESFAREVQALNG 335


Lambda     K      H
   0.319    0.137    0.406 

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: 274
Number of extensions: 14
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: 358
Length of database: 347
Length adjustment: 29
Effective length of query: 329
Effective length of database: 318
Effective search space:   104622
Effective search space used:   104622
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 (21.7 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