GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Synechococcus elongatus PCC 7942

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate Synpcc7942_0459 Synpcc7942_0459 glutathione-dependent formaldehyde dehydrogenase

Query= curated2:Q8R7K0
         (347 letters)



>FitnessBrowser__SynE:Synpcc7942_0459
          Length = 369

 Score =  104 bits (259), Expect = 4e-27
 Identities = 105/362 (29%), Positives = 159/362 (43%), Gaps = 50/362 (13%)

Query: 20  VKKEIPKIGPDEVLIKVKATSICGTDVHIYVWNEWAKSRIKP----PKTMGHEFVGEVVE 75
           V  + P+ G  EV++K+ AT +C TD        +  S   P    P  +GHE  G VVE
Sbjct: 20  VDVQAPQAG--EVMVKLVATGVCHTDA-------FTLSGADPEGIFPCILGHEGAGIVVE 70

Query: 76  IGENVTSVKVGDLVSAETHIVCGKCRACRTGNAHICE---NTLILGVDTDG--------- 123
           +GE VTSV VGD V       CG+C+ C++G  ++C+    T   G+  DG         
Sbjct: 71  VGEGVTSVAVGDHVIPLYTPECGECKFCKSGKTNLCQAIRATQGKGLMPDGTSRFSLNGQ 130

Query: 124 ---------AFAEYIKVPESNV-WINDKNIPLEILSIQEPLGNAVHTVFSGDVV--GKSV 171
                     F+EY  +PE  +  IN      ++  +   +   +  V +   V  G +V
Sbjct: 131 PIYHFMGTSTFSEYTVLPEIAIAKINPAAALDKVCLLGCGITTGIGAVLNTAKVEPGSTV 190

Query: 172 AVIGCGPIGMMAIPLLKRTGAAAIFAIEPADYRRELAHKLGATRVINPLRED--VVSIIK 229
           AV G G +G+  I       A+ I AI+    + E A +LGAT  INP   D  +  +I 
Sbjct: 191 AVFGLGGVGLSVIQGAVLAKASRILAIDINPDKAEFAKQLGATDFINPKDYDRPIQEVIV 250

Query: 230 SETEGYGADVVLDFSGNPTAIRQGLEYIAKG-GRMSILGLPD-----NEVPIDITNNVVF 283
             T+G G D   +  GN   +R  LE   KG G  +I+G+       +  P  +    V+
Sbjct: 251 ELTDG-GVDYSFEAIGNVNTMRAALESCHKGWGESTIIGVAGAGQEISTRPFQLVTGRVW 309

Query: 284 KGITIQGITGRRMYDTWYTVKGLLKSGLAEDLKPIITHTFPLTEYQKGMELMIKGQCGKV 343
           +G    G+ GR     +  V+  L   +  D    +T T PL E  +  E M  G+  + 
Sbjct: 310 RGSAFGGVKGRSQLPGY--VEQYLNGQIKVD--EFVTETRPLEEINEAFEDMHAGKVIRT 365

Query: 344 VL 345
           V+
Sbjct: 366 VI 367


Lambda     K      H
   0.319    0.139    0.414 

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: 348
Number of extensions: 25
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: 347
Length of database: 369
Length adjustment: 29
Effective length of query: 318
Effective length of database: 340
Effective search space:   108120
Effective search space used:   108120
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