GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdA in Pseudomonas putida KT2440

Align 2-keto-isovalerate dehydrogenase component α subunit (EC 1.2.4.4) (characterized)
to candidate PP_0555 PP_0555 Acetoin:2,6-dichlorophenolindophenol oxidoreductase subunit alpha

Query= metacyc::MONOMER-11683
         (330 letters)



>FitnessBrowser__Putida:PP_0555
          Length = 325

 Score =  155 bits (393), Expect = 1e-42
 Identities = 103/320 (32%), Positives = 165/320 (51%), Gaps = 5/320 (1%)

Query: 11  LTDQEAVDMYRTMLLARKIDERMWLLNRSGKIP-FVISCQGQEAAQVGAAFALDREMDYV 69
           L+ ++ +  Y  M   R  +ER+ +   +G+IP FV    G+EA+  G    L R+ D +
Sbjct: 5   LSTEQLLHAYEVMRTIRAFEERLHVEFATGEIPGFVHLYAGEEASAAGVMAHL-RDSDCI 63

Query: 70  LPYYRDMGVVLAFGMTAKDLMMSGFAKAADPNSGGRQMPGHFGQKKNRIVTGSSPVTTQV 129
              +R  G  +A G+    +M   + K      GG+    H    +  ++  +  V    
Sbjct: 64  ASTHRGHGHCIAKGVDVYGMMAEIYGKKTGV-CGGKGGSMHIADLEKGMLGANGIVGAGA 122

Query: 130 PHAVGIALAGRMEKKDIAAFVTFGEGSSNQGDFHEGANFAAVHKLPVIFMCENNKYAISV 189
           P   G ALA +++ +D  +   FG+G+SN+G   E  N A++  LP IF+ ENN YA + 
Sbjct: 123 PLVAGAALAAKLKGRDDVSVAFFGDGASNEGAVFEAMNMASIMNLPCIFVAENNGYAEAT 182

Query: 190 PYDKQVACENISDRAIGYGMPGVTVNGNDPLEVYQAVKEARERARRGEGPTLIETISYRL 249
             +  VAC++I+DRA G+GMPGVT++G D   VY+A   A ERAR G+GP+LIE    R 
Sbjct: 183 ASNWSVACDHIADRAAGFGMPGVTIDGFDFFAVYEAAGAAIERARSGQGPSLIEVKLSRY 242

Query: 250 TPHSSDDDDSSYRGREEVEEAKKS-DPLLTYQAYLKETGLLSDEIEQTMLDEIMAIVNEA 308
             H  + D  +YR  +EV+  ++S D L+ ++      GLL+ E    +   +  ++ +A
Sbjct: 243 YGH-FEGDAQTYRAPDEVKNLRESRDCLMQFRNKTTRAGLLTAEQLDAIDARVEDLIEDA 301

Query: 309 TDEAENAPYAAPESALDYVY 328
              A++ P   P   L  VY
Sbjct: 302 VRRAKSDPKPQPADLLTDVY 321


Lambda     K      H
   0.316    0.132    0.377 

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: 233
Number of extensions: 14
Number of successful extensions: 2
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: 330
Length of database: 325
Length adjustment: 28
Effective length of query: 302
Effective length of database: 297
Effective search space:    89694
Effective search space used:    89694
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 (21.6 bits)
S2: 48 (23.1 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