GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdB in Echinicola vietnamensis KMM 6221, DSM 17526

Align 2-keto-isovalerate dehydrogenase component β subunit (EC 1.2.4.4) (characterized)
to candidate Echvi_1750 Echvi_1750 Pyruvate/2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit

Query= metacyc::MONOMER-11684
         (327 letters)



>FitnessBrowser__Cola:Echvi_1750
          Length = 661

 Score =  271 bits (694), Expect = 3e-77
 Identities = 140/305 (45%), Positives = 198/305 (64%), Gaps = 6/305 (1%)

Query: 7   IDAINLAMKEEMERDSRVFVLGEDVGRKGGVFKATAGLYEQFGEERVMDTPLAESAIAGV 66
           +DAI+  ++  M + S + ++G+D+G  GG FK TAG   +FG ERV +TPL ESAI G 
Sbjct: 348 VDAISDGLRLSMRQFSNLVLMGQDIGEYGGAFKVTAGFLSEFGAERVRNTPLCESAIIGA 407

Query: 67  GIGAAMYGMRPIAEMQFADFIMPAVNQIISEAAKIRYRSNNDWSCPIVVRAPYGGGVHGA 126
            +G ++ G + + EMQFADF+    NQI++  AK+ YR        +V+R P G GV   
Sbjct: 408 ALGLSVKGFKSVVEMQFADFVSCGFNQIVNNLAKVHYRWGQH--ADVVIRMPTGAGVGAG 465

Query: 127 LYHSQSVEAIFANQPGLKIVMPSTPYDAKGLLKAAVRDEDPVLFFEHKRAYRLIKGEVPA 186
            +HSQS EA F + PGLKI+ PS+P DAKGLL AA+ D +P LFFEHK  YR + G+VP 
Sbjct: 466 PFHSQSNEAWFFHTPGLKILYPSSPQDAKGLLAAAIEDPNPCLFFEHKALYRSVIGQVPD 525

Query: 187 DDYVLPIGKADVKREGDDITVITYGLCVHFALQAAERLEKDGISAHVVDLRTVYPLDKEA 246
           + Y + IGKA + +EGD  TV+TYG+ VH+A +  E L+   +   ++DLRT+ P DKEA
Sbjct: 526 EYYTVEIGKAHLVKEGDQATVVTYGMGVHWAKRVMESLD---VRVDLLDLRTLLPWDKEA 582

Query: 247 IIEAASKTGKVLLVTEDTKEGSIMSEVAAIISEHCLFDLDAPIKRLAGPDIPAMPYAPTM 306
           + ++  KT KV+++ ED   G I +E+AA ISEHC   LDAP+ R    D P +P+A  +
Sbjct: 583 VEKSVKKTNKVMILHEDCLTGGIGAEIAAWISEHCFECLDAPVMREGSLDTP-VPFAANL 641

Query: 307 EKYFM 311
           E+ F+
Sbjct: 642 EENFL 646


Lambda     K      H
   0.319    0.136    0.392 

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: 518
Number of extensions: 17
Number of successful extensions: 3
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: 327
Length of database: 661
Length adjustment: 33
Effective length of query: 294
Effective length of database: 628
Effective search space:   184632
Effective search space used:   184632
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: 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