GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Dyella japonica UNC79MFTsu3.2

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate N515DRAFT_3331 N515DRAFT_3331 S-(hydroxymethyl)glutathione dehydrogenase / alcohol dehydrogenase

Query= curated2:Q72L62
         (343 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3331
          Length = 369

 Score =  122 bits (307), Expect = 1e-32
 Identities = 118/372 (31%), Positives = 162/372 (43%), Gaps = 42/372 (11%)

Query: 2   RALAKLAPEEGLTLVDRPVPEPGPGEILVRVEAASICGTDLHIWKWDAWARGRIRPPLVT 61
           RA     P + L +V+  V  P  GE+LVR+    +C TD      D    G    P V 
Sbjct: 4   RAAVAFGPGKPLEIVEIDVAPPRKGEVLVRITHTGVCHTDAFTLSGDD-PEGIF--PAVL 60

Query: 62  GHEFSGVVEAVGPGVKRPQVGDHVSLESHVVCHACPACRTGNYHVC---LNTKILGVDRD 118
           GHE  G+V  VG GV   + GDHV       C  C  C +G  ++C     T+  G+  D
Sbjct: 61  GHEGGGIVVEVGEGVSSVKPGDHVIPLYTAECRQCKFCLSGKTNLCQAVRATQGKGLMPD 120

Query: 119 GG------------------FAEYVVVPAEN-AWVNPKDLPFEVAAILE-PFGNAVHTVY 158
           G                   F+EY VVP  + A VNP+  P E   +L       +  V+
Sbjct: 121 GSTRFSYNGEPVYHYMGTSTFSEYTVVPEISLAVVNPQ-APLEKVCLLGCGVTTGIGAVH 179

Query: 159 AGSGVS-GKSVLITGAGPIGLMAAMVARASGAGPILVSDPNPYRLAFARPY-ADRLVNPL 216
             + V  G +V + G G IGL     A  + AG I+  D NP + A AR   A   VNP 
Sbjct: 180 NTAKVKPGDTVAVFGLGGIGLAVIQGAVQAKAGRIIGVDTNPGKFALAREMGATDCVNPR 239

Query: 217 E--EDLLEVVRRVTGSGVEVLLEFSGNEAAIHQGLMALIPG-GEARILGI--PSDPIR-- 269
           +    + EV+  +T  GV+   E  GN   +   L     G GE+ I+G+      IR  
Sbjct: 240 DHARPIQEVIVEMTDGGVDFSFECIGNVEVMRAALECCHKGWGESVIIGVAGAGQEIRTR 299

Query: 270 -FDLAGELVMRGITAFGIAGRRLWQTWMQG-TALVYSGRVDLSPLITHRLPLSRYREAFG 327
            F L    V RG    G+ GR    T + G       G + L P ITH LPL R  EAF 
Sbjct: 300 PFQLVTGRVWRGSAFGGVKGR----TQLPGMVEQAMQGEIRLDPFITHNLPLERINEAFE 355

Query: 328 LLASGQAVKVIL 339
           L+  G++++ ++
Sbjct: 356 LMHEGKSIRTVI 367


Lambda     K      H
   0.321    0.140    0.432 

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: 442
Number of extensions: 33
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: 343
Length of database: 369
Length adjustment: 29
Effective length of query: 314
Effective length of database: 340
Effective search space:   106760
Effective search space used:   106760
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 (21.8 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