GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdB in Luteimonas huabeiensis HB2

Align 2-oxoisovalerate dehydrogenase subunit beta; Branched-chain alpha-keto acid dehydrogenase E1 component beta chain; BCKDH E1-beta; EC 1.2.4.4 (characterized)
to candidate WP_024891572.1 Z164_RS0115365 alpha-ketoacid dehydrogenase subunit beta

Query= SwissProt::Q5SLR3
         (324 letters)



>NCBI__GCF_000559025.1:WP_024891572.1
          Length = 347

 Score =  309 bits (791), Expect = 7e-89
 Identities = 157/322 (48%), Positives = 219/322 (68%), Gaps = 1/322 (0%)

Query: 2   ALMTMVQALNRALDEEMAKDPRVVVLGEDVGKRGGVFLVTEGLLQKYGPDRVMDTPLSEA 61
           A +T+++A+ +AL  EM  D  VVVLGEDVG  GGVF  T GL Q++GP RV+DTPL E 
Sbjct: 23  APITLIEAITQALAWEMRHDDSVVVLGEDVGVNGGVFRATAGLQQRFGPGRVLDTPLDET 82

Query: 62  AIVGAALGMAAHGLRPVAEIQFADYIFPGFDQLVSQVAKLRYRSGGQFTAPLVVRMPSGG 121
            I G  +GMAA G++PVAE QF  +++P  D +V   A+ RYR+ G+   P+V+R+P GG
Sbjct: 83  TIAGLTVGMAAMGMKPVAEAQFDGFMYPMVDHIVCHAARFRYRTRGRLHCPMVLRVPWGG 142

Query: 122 GVRGGHHHSQSPEAHFVHTAGLKVVAVSTPYDAKGLLKAAIRDEDPVVFLEPKRLYRSVK 181
           G+R   HHS++ EA F +  GL+VV  S+P  A GLL AAIR+ DPV++ EPKR+YR  K
Sbjct: 143 GIRAPEHHSEANEAIFTNVPGLRVVMPSSPARAYGLLLAAIREPDPVIYFEPKRIYRQYK 202

Query: 182 EEVPEEDYTLPIGKAALRREGKDLTLIGYGTVMPEVLQAAAELAKAGVSAEVLDLRTLMP 241
           E VP++   LP+    + R+G D+TL+ +G  + E L+AA  LA+ G+ AEV+D+ TL P
Sbjct: 203 ERVPDDGEALPLDVCYVLRDGTDITLVTWGAQVKETLEAADRLAEEGIGAEVIDVATLRP 262

Query: 242 WDYEAVMNSVAKTGRVVLVSDAPRHASFVSEVAATIAEDLLDMLLAPPIRVTGFDTPYP- 300
            D+  +  SVA+TGR V+V +AP+ A F +E+AA +AE+ +  LLAP  RV G+DT  P 
Sbjct: 263 LDFATIAESVARTGRCVIVHEAPKTAGFGAEIAARLAEECMYDLLAPVERVAGYDTHIPL 322

Query: 301 YAQDKLYLPTVTRILNAAKRAL 322
           +  +  YLP+  RI+ AAKRAL
Sbjct: 323 FRLEMKYLPSTARIVEAAKRAL 344


Lambda     K      H
   0.319    0.136    0.389 

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: 289
Number of extensions: 7
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: 324
Length of database: 347
Length adjustment: 28
Effective length of query: 296
Effective length of database: 319
Effective search space:    94424
Effective search space used:    94424
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 24 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