GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Sphingomonas koreensis DSMZ 15582

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate Ga0059261_0846 Ga0059261_0846 Zn-dependent alcohol dehydrogenases, class III

Query= curated2:Q72L62
         (343 letters)



>FitnessBrowser__Korea:Ga0059261_0846
          Length = 361

 Score =  128 bits (321), Expect = 3e-34
 Identities = 107/366 (29%), Positives = 166/366 (45%), Gaps = 33/366 (9%)

Query: 1   MRALAKLAPEEGLTLVDRPVPEPGPGEILVRVEAASICGTDLHIWKWDAWARGRIRPPLV 60
           ++A      +  L + D  + +PGP E+L+R  A  +C +DLH       A   + P  +
Sbjct: 1   VKAAVLFEAKRPLEIHDITIDKPGPREVLIRTAACGVCRSDLHFVDG---AYPHVMPT-I 56

Query: 61  TGHEFSGVVEAVGPGVKRPQVGDHVSLESHVVCHACPACRTGNYHVCLN----------- 109
            GHE SGVVEAVG  V R + GDHV     V C +C  C +G   +C++           
Sbjct: 57  PGHEASGVVEAVGSEVTRLRPGDHVITFFTVFCGSCEFCVSGRPSLCVDGSTKRPKEGEP 116

Query: 110 -------TKILGVDRDGGFAEYVVVPAENAWVNPKDLPFEVAAILEPFGNAVHT----VY 158
                  T I        FAE ++V         KD+P + AA+L   G AV T    ++
Sbjct: 117 KLRLPDGTPIAQFLNLSAFAEQMLVHENACVAISKDMPLDRAALL---GCAVITGAGAIF 173

Query: 159 AGSGVS-GKSVLITGAGPIGLMAAMVARASGAGPILVSDPNPYRLAFARPY-ADRLVNPL 216
             S V+ G++V + G G IGL A   A+ +GAG I+  DP P +   AR   A  + + +
Sbjct: 174 RDSKVTPGETVAVIGCGGIGLSAVNAAKIAGAGKIIAIDPVPEKREIARKMGATHVFDAM 233

Query: 217 EEDLLEVVRRVTGSGVEVLLEFSGNEAAIHQGLMALIPGGEARILGIPSDPIRFDLAGEL 276
            +DL++ V ++T  GV+  +E  G           L  GG A ILG+ +      + G  
Sbjct: 234 ADDLVKQVAKLTDGGVDYAIEAVGRPNTAELAWNLLRRGGTATILGMIAPGQSVSIPGPT 293

Query: 277 VMRGITAFG-IAGRRLWQTWMQGTALVY-SGRVDLSPLITHRLPLSRYREAFGLLASGQA 334
            + G    G + G   +   +     +Y  G +DL  ++  R+ L     AF  L  G A
Sbjct: 294 FLTGKKLQGSLLGSMRFPVDLPRLVQMYLDGLLDLDTMVAERIRLEDINHAFDNLRKGDA 353

Query: 335 VKVILD 340
           V+ +++
Sbjct: 354 VRSVIE 359


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: 374
Number of extensions: 21
Number of successful extensions: 5
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: 361
Length adjustment: 29
Effective length of query: 314
Effective length of database: 332
Effective search space:   104248
Effective search space used:   104248
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