GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Echinicola vietnamensis KMM 6221, DSM 17526

Align L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized)
to candidate Echvi_4558 Echvi_4558 putative phosphonate catabolism associated alcohol dehydrogenase

Query= SwissProt::Q8U259
         (348 letters)



>FitnessBrowser__Cola:Echvi_4558
          Length = 358

 Score = 74.3 bits (181), Expect = 4e-18
 Identities = 84/346 (24%), Positives = 151/346 (43%), Gaps = 39/346 (11%)

Query: 20  VEVDVPKPGPGEVLIKILATSICGTDLHIYEWNEWAQTRIRPPQIMGHEVAGEVVEVGPG 79
           + V  P    GE+L++ L  +IC +DLH +      + +     ++GHE+ G +  +   
Sbjct: 21  LSVAFPSLQKGEILVRNLYATICASDLHTFH----GRRKSCHHSVLGHEIVGRIEALAE- 75

Query: 80  VEG--------IEVGDYVSVETHIVCGKCYACKRGQYHVCQNTKIFGVDT-------DGV 124
            EG        +E GD ++   +          +G     ++   +G +        +G 
Sbjct: 76  -EGAKDYHGRPLEKGDRITWSVYAHDPASPTSLKGFPQKSEDLYKYGHEQIDDHYQLNGG 134

Query: 125 FAEYAVV-PAQNVWKNPKNIPPEYATLQEPLGNAVDTV-----LAGPIAGKSVLITGAGP 178
           F+ +  +    +++K P+ +    A    PL     T+     LAG ++GK+VL+ GAG 
Sbjct: 135 FSTHCHLRKGTSLFKLPEALTDREAA---PLNCTHATIAGAMRLAGSLSGKTVLVNGAGM 191

Query: 179 LGLLGIAVAKASGAYPVIVSEPSEFRRNLAKKVGADYVINPFEEDVVKEVMDITDGNGVD 238
           LGL   A+AK  GA  V   + S  +   AK  GAD       +DV   +      +  D
Sbjct: 192 LGLSACAMAKEKGASHVWACDLSIEKATHAKAFGADTAFEAESKDVPHRIF---GPDKAD 248

Query: 239 VFLEFSGAPKALEQGLQAVTPAGRVSLLG-LFPGKVSIDFNNLIIFKALTVYGITGRHLW 297
           + +E SG P+A+E  L  +   G + L+G +FP +        ++   LT+ G+      
Sbjct: 249 IIIETSGMPEAMENCLHMLGIGGTIILVGAVFPQRNLSINAEFLVRNLLTIKGLHNYIPE 308

Query: 298 ETWYTVSRLLQS-GKLNIDPIITHKYKGFDKYEEAFELMRAGKTGK 342
           +    +S L ++  K   D ++  ++   ++ + AFE   AG  GK
Sbjct: 309 DLATAISFLTKAKAKYPFDSLVGREF-SLEQLDSAFE---AGSHGK 350


Lambda     K      H
   0.318    0.138    0.417 

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: 253
Number of extensions: 18
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 348
Length of database: 358
Length adjustment: 29
Effective length of query: 319
Effective length of database: 329
Effective search space:   104951
Effective search space used:   104951
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 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