GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Cupriavidus basilensis 4G11

Align L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized)
to candidate RR42_RS09405 RR42_RS09405 butanediol dehydrogenase

Query= SwissProt::Q8U259
         (348 letters)



>FitnessBrowser__Cup4G11:RR42_RS09405
          Length = 357

 Score =  186 bits (472), Expect = 8e-52
 Identities = 116/339 (34%), Positives = 180/339 (53%), Gaps = 15/339 (4%)

Query: 21  EVDVP-KPGPGEVLIKILATSICGTDLHIYEW--------NEWAQTRIRPPQIMGHEVAG 71
           EV VP KP  G V I++    ICG+DLH Y          +    T ++   I+GHE +G
Sbjct: 16  EVRVPDKPAEGWVKIRVHWCGICGSDLHEYVAGPVFIPVDHPHPLTGLKGQCILGHEFSG 75

Query: 72  EVVEVGPGVEGIEVGDYVSVETHIVCGKCYACKRGQYHVCQNTKIFGVDTDGVFAEYAVV 131
           E+ E+G GV G +VG+ V+ +    CGKCY C  G Y++C++    G+  +G FAEY  V
Sbjct: 76  EIAELGAGVTGFKVGERVTADACQHCGKCYYCTHGLYNICESLAFTGLMNNGAFAEYVNV 135

Query: 132 PAQNVWKNPKNIPPEYATLQEPLGNAVDTV-LAGPIAGKSVLITGAGPLGLLGIAVAKAS 190
           PA+ ++K P+N P E   L EPL   +  V  AG I G++V++ GAG +GL  I  AKA+
Sbjct: 136 PAELLYKLPENFPTEAGALIEPLAVGLHAVKKAGNIVGQTVVVVGAGTIGLCTIMCAKAA 195

Query: 191 GAYPVIVSEPSEFRRNLAKKVGADYVINPFEEDVVKEVMDITDGNGVDVFLEFSGAPKAL 250
           GA  +I  E S  R+  A +VGA+ VI+P E D + +V  +T G G DV  E  G     
Sbjct: 196 GAGRIIALEMSSARKKKALEVGANVVIDPKECDAIAQVKALTGGYGADVSFECIGNKATA 255

Query: 251 EQGLQAVTPAGRVSLLGLFPGKVSIDFNNLIIFKALTVYGITGRHLWETWYT-VSRLLQS 309
           +  +  +  AG+  ++G+F    + +F  ++     T   I G   +   +  V R +  
Sbjct: 256 KLAIDVIRKAGKCVMVGIFEEPSAFNFFEIV----STEKEIIGSLAYNGEFADVIRFIAD 311

Query: 310 GKLNIDPIITHKYKGFDKYEEAFELMRAGKTGKVVFMLK 348
           G++++ P+IT +    D   + FE +   K G V  +++
Sbjct: 312 GRIDVQPLITGRISLADIVSQGFEELVNNKDGNVKIIVQ 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: 323
Number of extensions: 19
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: 357
Length adjustment: 29
Effective length of query: 319
Effective length of database: 328
Effective search space:   104632
Effective search space used:   104632
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