GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdA in Pedobacter sp. GW460-11-11-14-LB5

Align 2-keto-isovalerate dehydrogenase component α subunit (EC 1.2.4.4) (characterized)
to candidate CA265_RS18405 CA265_RS18405 dehydrogenase

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



>FitnessBrowser__Pedo557:CA265_RS18405
          Length = 658

 Score =  187 bits (474), Expect = 8e-52
 Identities = 110/309 (35%), Positives = 178/309 (57%), Gaps = 18/309 (5%)

Query: 13  DQEAVDMYRTMLLARKIDERMWLLNRSGKIPFVISCQGQEAAQVGAAFALDREMDYVLPY 72
           D+  +++YR +L  R ++++M  L R G+I    S  GQEA  VG+  A+  + +Y+LP 
Sbjct: 10  DKFLLNLYRRLLYPRMVEDKMLKLLRQGRIGKWFSGIGQEAIAVGSTLAMQSD-EYILPM 68

Query: 73  YRDMGVVLAFGMTAKDLM------MSGFAKAADPNSGGRQMPGHFGQKKNRIVTGSSPVT 126
           +R++GV  +  +  K LM      ++GF+K       GR    HFG ++ +I+   S + 
Sbjct: 69  HRNLGVFTSRDIPLKKLMAQWQGKITGFSK-------GRDRSFHFGTQEYKIIGMISHLG 121

Query: 127 TQVPHAVGIALAGRMEKKDIAAFVTFGEGSSNQGDFHEGANFAAVHKLPVIFMCENNKYA 186
            Q+  A GIALA  +  +  A  V  GEG++++GDFHE  N AAV  LPVIF+ ENN Y 
Sbjct: 122 PQMALADGIALADVLRNQPHATLVYTGEGATSEGDFHEAVNVAAVWNLPVIFLIENNGYG 181

Query: 187 ISVPYDKQVACENISDRAIGYGMPGVTVNGNDPLEVYQAVKEARERARRGEGPTLIETIS 246
           +S P  +Q  C+N+ D+AIGYG+ G+ ++GN+ LEVY  + +     R+   P L+E ++
Sbjct: 182 LSTPKSEQFRCKNLVDKAIGYGVEGIQIDGNNILEVYDTINQLAMEIRKDPRPVLVECLT 241

Query: 247 YRLTPHSSDDDDSSYRGREEVEEAKKSDPLLTYQAYLKETGLLSDEIEQTMLDEIMAIVN 306
           +R+  H  +   + Y  +E  +E +K DPL  Y+AYL E G+L+ +   T++D  + +  
Sbjct: 242 FRMRGH-EEASGTKYVPQELFDEWEKKDPLNNYEAYLIEQGVLTPD---TVIDIKIQVKR 297

Query: 307 EATDEAENA 315
           +   E E A
Sbjct: 298 DIELEIEEA 306


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: 469
Number of extensions: 21
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 330
Length of database: 658
Length adjustment: 33
Effective length of query: 297
Effective length of database: 625
Effective search space:   185625
Effective search space used:   185625
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: 51 (24.3 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