GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Burkholderia phytofirmans PsJN

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate BPHYT_RS28135 BPHYT_RS28135 alcohol dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__BFirm:BPHYT_RS28135
          Length = 339

 Score =  170 bits (430), Expect = 6e-47
 Identities = 109/320 (34%), Positives = 160/320 (50%), Gaps = 13/320 (4%)

Query: 36  GEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGHEIVGVVTEVGSKVEKVKVGDNVG 95
           G   V +K+  CG+CHSD       W    YP VPGHEI GV+  VG+ VE    G  VG
Sbjct: 27  GAGQVLIKIQACGICHSDVLTKEGQWPGLEYPRVPGHEIAGVIDTVGAGVEGWAAGQRVG 86

Query: 96  IGCLVGSCRSCESCCDNRESHCENTIDTYGSIYFDGTMTHGGYSDTMVADEHFILRWPKN 155
           +G   G C  CE C       C+  +         G    GGY++ MVA    + R P +
Sbjct: 87  VGWHGGHCGRCEHCRRGDFVLCQRAL-------VPGISYDGGYAEFMVAPVEALARIPDD 139

Query: 156 LPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVVGLGGLGHVAVKMAKAFGAQVTVIDI 215
           L     APLLCAGITT++ L+  G  + G  + V+G+GGLGH+ V+ A+  G     I  
Sbjct: 140 LSDVDAAPLLCAGITTFNALRNSGA-RAGDVVAVLGIGGLGHLGVQFARKMGFVTVAIAR 198

Query: 216 SESKRKEALEKLGADSFLLNSDQEQMKGARSSLDG---IIDTVPVNHPLAPLFDLLKPNG 272
            + K   A E LGA  + ++S    +  A  +L G   I+ TV     ++ +   L  NG
Sbjct: 199 GQDKASLAKE-LGAHHY-IDSTTANVAQALQALGGARVILATVTSGKAMSAVVGGLGLNG 256

Query: 273 KLVMVGAPEKPFELPVFSLLKGRKLLGGTINGGIKETQEMLDFAAKHNITADVEVIPMDY 332
           KL+MVG  E+P E+P+   + GR  + G  +G   ++Q+ L F+A   I   +E  P+  
Sbjct: 257 KLIMVGLSEEPVEVPIAQFIMGRNSVQGWPSGTSADSQDTLAFSALSGIKPMIEEFPLTK 316

Query: 333 VNTAMERLVKSDVRYRFVID 352
              A +R++    R+R V++
Sbjct: 317 AAEAYDRMMSGAARFRVVLN 336


Lambda     K      H
   0.319    0.137    0.415 

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: 305
Number of extensions: 11
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: 365
Length of database: 339
Length adjustment: 29
Effective length of query: 336
Effective length of database: 310
Effective search space:   104160
Effective search space used:   104160
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