GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Thauera aminoaromatica S2

Align L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized)
to candidate WP_004309492.1 C665_RS11135 L-threonine 3-dehydrogenase

Query= SwissProt::Q8U259
         (348 letters)



>NCBI__GCF_000310185.1:WP_004309492.1
          Length = 345

 Score =  289 bits (740), Expect = 6e-83
 Identities = 145/340 (42%), Positives = 215/340 (63%), Gaps = 3/340 (0%)

Query: 5   MVAIMKTKPEYGAELVEVDVPKPGPGEVLIKILATSICGTDLHIYEWNEWAQTRIRPPQI 64
           M A+ K  P  G  L  V+ P+ GP +VLIKI  T+ICGTD+HI++W+EWAQ  I  P  
Sbjct: 1   MKALAKLTPSVGLTLTSVEKPEVGPNDVLIKIKKTAICGTDIHIWKWDEWAQKTIPVPMH 60

Query: 65  MGHEVAGEVVEVGPGVEGIEVGDYVSVETHIVCGKCYACKRGQYHVCQNTKIFGVDTDGV 124
           +GHE  G + E+G  V G ++GD VS E HI CG C  C+ G+ H+C+NT   GV+  G 
Sbjct: 61  VGHEYVGVIAEMGQEVRGFKIGDRVSGEGHITCGFCRNCRAGRRHLCRNTVGVGVNRAGA 120

Query: 125 FAEYAVVPAQNVWKNPKNIPPEYATLQEPLGNAVDTVLAGPIAGKSVLITGAGPLGLLGI 184
           FAEY  +PA N +K P +I  + A + +P GNA  T L+  + G+ VLITGAGP+G++ +
Sbjct: 121 FAEYLAIPAVNAFKIPDDISDDLAAIFDPFGNATHTALSFNLVGEDVLITGAGPIGIMAV 180

Query: 185 AVAKASGAYPVIVSEPSEFRRNLAKKVGADYVINPFEEDVVKEVMDITDGNGVDVFLEFS 244
           A+A+  GA  V++++ ++ R  LA+K+GA   +N   E++     ++    G DV LE S
Sbjct: 181 AIARHVGARHVVITDVNDHRLELARKMGATRAVNVSRENLADVKTELHMVEGFDVGLEMS 240

Query: 245 GAPKALEQGLQAVTPAGRVSLLGLFPGKVSIDFNNLIIFKALTVYGITGRHLWETWYTVS 304
           G P A    L+ +   G+++LLG+ P   +ID+N  +IFK L + GI GR ++ETWY + 
Sbjct: 241 GVPSAFTSMLEHMNHGGKIALLGIPPSNTAIDWNQ-VIFKGLEIKGIYGREMFETWYKMV 299

Query: 305 RLLQSGKLNIDPIITHKYKGFDKYEEAFELMRAGKTGKVV 344
            +LQSG L++ PIITH Y   ++++  FE M +G +GKV+
Sbjct: 300 AMLQSG-LDLSPIITHHYP-VEEFKTGFETMLSGNSGKVI 337


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: 328
Number of extensions: 9
Number of successful extensions: 4
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: 345
Length adjustment: 29
Effective length of query: 319
Effective length of database: 316
Effective search space:   100804
Effective search space used:   100804
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