GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Neptunomonas antarctica S3-22

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate WP_054343403.1 Nant_RS19780 S-(hydroxymethyl)glutathione dehydrogenase/class III alcohol dehydrogenase

Query= curated2:Q8R7K0
         (347 letters)



>NCBI__GCF_001305295.1:WP_054343403.1
          Length = 376

 Score =  113 bits (282), Expect = 9e-30
 Identities = 105/356 (29%), Positives = 159/356 (44%), Gaps = 56/356 (15%)

Query: 31  EVLIKVKATSICGTDVHIYVWNEWAKSRIKP----PKTMGHEFVGEVVEIGENVTSVKVG 86
           EV +++ A+ +C TD        +  S   P    P  +GHE  G V  IGE VTSV VG
Sbjct: 34  EVRVRIVASGVCHTDA-------FTLSGDDPEGIFPAILGHEGAGIVESIGEGVTSVAVG 86

Query: 87  DLVSAETHIVCGKCRACRTGNAHICE---NTLILGVDTDG------------------AF 125
           D V       CG+C+ C++G  ++C+    T   G+  DG                   F
Sbjct: 87  DHVIPLYTPECGECKFCKSGKTNLCQKIRETQGKGLMPDGTTRFHKDGQPIFHYMGCSTF 146

Query: 126 AEYIKVPESNVWINDKNIPLEIL-----SIQEPLGNAVHTVFSGDVVGKSVAVIGCGPIG 180
           +EY  +PE ++   +K+ PLE +      +   +G  ++T    +  G +VA+ G G IG
Sbjct: 147 SEYTVLPEISLAKVNKDAPLEEICLLGCGVTTGMGAVMNTAKVEE--GATVAIFGIGGIG 204

Query: 181 MMAIPLLKRTGAAAIFAIEPADYRRELAHKLGATRVINPLRED--VVSIIKSETEGYGAD 238
           + AI       A+ I AI+  + + ELA KLGAT  INP   D  +  +I   T+G G D
Sbjct: 205 LSAIIGATMAKASRIIAIDINESKFELARKLGATDCINPKDYDKPIQDVIVELTDG-GVD 263

Query: 239 VVLDFSGNPTAIRQGLEYIAKGGRMSIL------GLPDNEVPIDITNNVVFKGITIQGIT 292
              +  GN   +R  LE   KG   S++      G   +  P  +    V++G    G+ 
Sbjct: 264 YSFECIGNVNVMRSALECCHKGWGESVVIGVAGAGQEISTRPFQLVTGRVWRGSAFGGVK 323

Query: 293 GRRMYDTWYT--VKGLLKSGLAEDLKPIITHTFPLTEYQKGMELMIKGQCGKVVLY 346
           GR     +    +KG  K      L   ITHT  L E     +LM +G+  + V++
Sbjct: 324 GRSELPDFVERYMKGEFK------LDDFITHTMTLEEINTAFDLMHEGKSIRSVIH 373


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: 342
Number of extensions: 20
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: 347
Length of database: 376
Length adjustment: 29
Effective length of query: 318
Effective length of database: 347
Effective search space:   110346
Effective search space used:   110346
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 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