GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Pseudomonas simiae WCS417

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate GFF3461 PS417_17720 iditol 2-dehydrogenase

Query= BRENDA::O58389
         (348 letters)



>FitnessBrowser__WCS417:GFF3461
          Length = 359

 Score =  162 bits (410), Expect = 1e-44
 Identities = 114/343 (33%), Positives = 173/343 (50%), Gaps = 25/343 (7%)

Query: 19  LVEVDVPKPGPGEVLIKVLATSICGTDLHIYE-----W---NEWAQSRIKPPQIMGHEVA 70
           L  +  P+    E++I++ A  IC +D   +      W   N W    +K P + GHE  
Sbjct: 20  LERIGKPQARANELVIRIAACGICASDCKCHSGAAMFWGGDNPW----VKAPVVPGHEFF 75

Query: 71  GEVVEIGPGVEG---IEVGDYVSVETHIVCGKCYACRRGQYHVCQNTKIFGVD---TDGV 124
           G VVE G G E    + VGD V  E  + CGKC  C+ G+Y +C+   IFG      +G 
Sbjct: 76  GYVVEAGEGAEEHFEVAVGDKVIAEQIVPCGKCRFCKSGKYWMCEVHNIFGFQREVAEGG 135

Query: 125 FAEYAVVPAQNI-WKNPKSIPPEYATLQEPLGNAVDTVLAGPIS-GKSVLITGAGPLGLL 182
            A+Y  +P   I  K P+S+  E + L EP+  ++ TV  G I     V+I GAG LGL 
Sbjct: 136 MAQYMRIPKTAIVHKIPESVSLEDSALVEPMACSIHTVNRGDIQLDDVVVIAGAGTLGLC 195

Query: 183 GIAVAKASGAYPVIVSEPSDFRRELAKKVGADYVINPFEEDVVKEVMDITDGNGVDVFLE 242
            + VA       ++V +  D R ELAKK GAD VINP  ++  + +  +TD  G DV++E
Sbjct: 196 MVQVAALKTPKKLVVIDMVDERLELAKKFGADVVINPSRDNAREIINGLTDNYGCDVYIE 255

Query: 243 FSGAPKALEQGLQAVTPAGRVSLLGLYPGKVTIDFNNLIIFKALTIYGITGRHLWETWYT 302
            +G P  + QGL  +   GR     ++  + ++D++ +   K L    + G HL    Y 
Sbjct: 256 TTGVPAGVTQGLDLIRKLGRFVEFSVFGAETSVDWSIIGDRKEL---DVRGAHLGPYCYP 312

Query: 303 VS-RLLQSGKLNLDPIITHKYKGFDKYEEAFELMRAGKTGKVV 344
           ++  L + G +    I+TH +   D + EAFEL  + K+ KV+
Sbjct: 313 IAIDLFERGLVTSKGIVTHDFP-LDDWAEAFELANSTKSIKVL 354


Lambda     K      H
   0.318    0.139    0.418 

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: 315
Number of extensions: 18
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: 359
Length adjustment: 29
Effective length of query: 319
Effective length of database: 330
Effective search space:   105270
Effective search space used:   105270
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