GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Pseudomonas stutzeri RCH2

Align D-sorbitol dehydrogenase (EC 1.1.1.14; EC 1.1.1.9) (characterized)
to candidate GFF875 Psest_0895 Threonine dehydrogenase and related Zn-dependent dehydrogenases

Query= metacyc::MONOMER-13193
         (363 letters)



>FitnessBrowser__psRCH2:GFF875
          Length = 379

 Score =  114 bits (285), Expect = 4e-30
 Identities = 101/331 (30%), Positives = 137/331 (41%), Gaps = 25/331 (7%)

Query: 15  SFVLNKPGDVTFEERPKPTITDPNDVLVAVNYTGICGSDVHYWVHGAIGHFVVKDPMVLG 74
           + V N P DV+ +  P   I  P D LV V  T ICGSD+H +     G    +   V G
Sbjct: 3   AIVYNGPRDVSVQNVPDAKIERPTDALVRVTSTNICGSDLHMYE----GRTTFETGRVFG 58

Query: 75  HESAGTVVEVGPAVKSLKPGDRVALEPGYPCRRCSFCRAGKYNLC----PDMV-----FA 125
           HE+ G VVEVG  V+ +K GD V L     C  C  C  G    C    P        FA
Sbjct: 59  HENLGEVVEVGAGVERVKVGDMVCLPFNIGCGFCENCEKGLTGYCLTANPGSAGAAYGFA 118

Query: 126 ATPPYHGTLTGLWAAP-ADF-CYKLPDGVSLQEG---ALIEPLAVAVHIVKQARVQPGQS 180
               Y G    L   P ADF C  LP+    +E     L +      H  + A +QPG+S
Sbjct: 119 EMGTYDGGQAELLRVPFADFNCLVLPEDAKEREDDYVMLSDIFPTGWHATRLAGLQPGES 178

Query: 181 VVVMGAGPVGLLCAAVAKAYGASTIVSVDIVQSKLDFARGFCSTHTYVSQRISAEDNAKA 240
           + + GAGPVGL+ A  A   GAS +  +D    +L  A    +T    S    A D    
Sbjct: 179 IAIYGAGPVGLMAAHSALIQGASQVFVIDDQPDRLKLAAQMGAT-PINSVEQKAVDEILN 237

Query: 241 IKELAGLPGGADVV----IDASGAEPSIQTSIHVVRMGGTYVQGGMGKSDITFPIMAMCL 296
             +  G   G + V     D  G E +  T  ++V    T   GG+G   +  P      
Sbjct: 238 YTDGKGTDRGCECVGYQCCDKHGHEVNHLTMNNLV--ASTKATGGIGVVGLFVPQDPGAK 295

Query: 297 KEVTVRGSFRYGAGDYELAVELVRTGRVDVK 327
            E+   G   +  G +    + + TG+ +VK
Sbjct: 296 NELAKEGKMAFDFGSFWFKGQKIGTGQANVK 326


Lambda     K      H
   0.319    0.136    0.406 

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: 366
Number of extensions: 21
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: 363
Length of database: 379
Length adjustment: 30
Effective length of query: 333
Effective length of database: 349
Effective search space:   116217
Effective search space used:   116217
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