GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Skermanella stibiiresistens SB22

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate WP_037458740.1 N825_RS26665 2,3-butanediol dehydrogenase

Query= BRENDA::O58389
         (348 letters)



>NCBI__GCF_000576635.1:WP_037458740.1
          Length = 355

 Score =  150 bits (379), Expect = 5e-41
 Identities = 111/343 (32%), Positives = 177/343 (51%), Gaps = 18/343 (5%)

Query: 9   MKTKPGYGAELVEVDV-----PKPGPGEVLIKVLATSICGTDLHIYEWNEWAQSR----- 58
           MK+   + A  V VD       +P PG+VL++     ICGTDLH Y        R     
Sbjct: 1   MKSVRFHAARDVRVDSVAAPPDRPAPGQVLVRNRFCGICGTDLHEYVAGPIFIPREPHPY 60

Query: 59  --IKPPQIMGHEVAGEVVEIGPGVEGIEVGDYVSVETHIVCGKCYACRRGQYHVCQNTKI 116
                PQI+GHE  G VV +G GV  ++ GD VS++  I     +  RRG Y +     +
Sbjct: 61  TGASGPQILGHEFGGTVVAVGDGVTIVKPGDRVSIQPLIAPRDDHFGRRGLYQLSDQLGL 120

Query: 117 FGVDTD-GVFAEYAVVPAQNIWKNPKSIPPEYATLQEPLGNAVDTV-LAGPISGKSVLIT 174
            G+    G  AEY+V+   N+++ P ++  E + L EP   AV  +  +G  +G+S LIT
Sbjct: 121 VGLSWAWGGMAEYSVLNDYNVFRMPDAVSDEQSALIEPAAVAVYAIDRSGLRAGESALIT 180

Query: 175 GAGPLGLLGIAVAKASGAYPVIVSEPSDFRRELAKKVGADYV-INPFEEDVVKEVMDITD 233
           GAGP+G L +  A+A+GA  + +S+ +D R  + + +  D + INP  E++V+ V D T+
Sbjct: 181 GAGPIGALTMLAARAAGASKIFISDTNDNRLRMMRDILPDCITINPGTENLVEAVRDRTE 240

Query: 234 GN-GVDVFLEFSGAPKALEQGLQAVTPAGRVSLLGLYPGKVTIDFNNLIIFKALTIYGIT 292
           G  G DV LE  G   AL   + AV   G V  +GL+    T+D    I FK + + G +
Sbjct: 241 GQVGADVALECVGHGGALADCVNAVRRQGTVVQVGLHVKPATVD-GFAITFKDIDLRG-S 298

Query: 293 GRHLWETWYTVSRLLQSGKLNLDPIITHKYKGFDKYEEAFELM 335
             +  ++W  V+ ++++G   ++ ++T +    D   + FE +
Sbjct: 299 WTYPTQSWPRVASMVEAGIFPVEKVVTKRIALDDVVSQGFEAL 341


Lambda     K      H
   0.318    0.139    0.418 

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: 318
Number of extensions: 19
Number of successful extensions: 8
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: 348
Length of database: 355
Length adjustment: 29
Effective length of query: 319
Effective length of database: 326
Effective search space:   103994
Effective search space used:   103994
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 24 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