GapMind for catabolism of small carbon sources

 

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

Align threonine ammonia-lyase; EC 4.3.1.19 (characterized)
to candidate Echvi_1189 Echvi_1189 Threonine dehydratase

Query= CharProtDB::CH_024588
         (329 letters)



>FitnessBrowser__Cola:Echvi_1189
          Length = 319

 Score =  172 bits (437), Expect = 8e-48
 Identities = 106/320 (33%), Positives = 167/320 (52%), Gaps = 4/320 (1%)

Query: 1   MHITYDLPVAIDDIIEAKQRLAGRIYKTGMPRSNYFSERCKGEIFLKFENMQRTGSFKIR 60
           M  TY +P  ID I +A QR+   I+ T +      ++    +++ K EN Q+ G+FK R
Sbjct: 1   MQQTYRIPQLID-IKQAYQRIMAYIHHTPILTCEAINKMADCQLYFKCENFQKVGAFKAR 59

Query: 61  GAFNKLSSLTDAEKRKGVVACSAGNHAQGVSLSCAMLGIDGKVVMPKGAPKSKVAATCDY 120
           GA N +  L    K+ GV   S+GNHA  ++ +    G    +VMP  A   K AA   Y
Sbjct: 60  GATNAILKLPPGLKKNGVATHSSGNHAAALARAAKETGTKAYIVMPSTAAAIKKAAVRTY 119

Query: 121 SAEVVLHGDNFNDTIAKVSEIVEMEGRIFIPPYDDPKVIAGQGTIGLEIMEDLYDVDNVI 180
             E++    N       + ++VE  G  FIPPYD   VI GQ T  LE+ ++    D +I
Sbjct: 120 GGEIIECEPNLKARETTLEKVVEETGAAFIPPYDYMDVIEGQATCALEMWDEGIPFDAII 179

Query: 181 VPIGGGGLIAGIAVAIKSINPTIRVIGVQSENVHGMAASFHSGEITTHRTTGTLADGCDV 240
            P+GGGGL+AG A+    ++    V G + +       S  + +I       T+ADG  +
Sbjct: 180 TPVGGGGLLAGTALTTHYLSRKTPVYGAEPKGADDAYRSLKANKIIPMENPNTIADGL-L 238

Query: 241 SRPGNLTYEIVRELVDDIVLVSEDEIRNSMIALIQRNKVVTEGAGALACAALLSGKLDQY 300
           +  G   + I+ + V DI+ VS+D+I  +M  + +R K+V E + A+  AA+L+ K    
Sbjct: 239 TSLGKRNFTIISKNVADILTVSDDQIIAAMRLVFERMKLVIEPSSAVPLAAILANK--PL 296

Query: 301 IQNRKTVSIISGGNIDLSRV 320
            QN++   +ISGGN+D+S++
Sbjct: 297 FQNKRVGIVISGGNVDVSKL 316


Lambda     K      H
   0.318    0.136    0.386 

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: 211
Number of extensions: 8
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: 329
Length of database: 319
Length adjustment: 28
Effective length of query: 301
Effective length of database: 291
Effective search space:    87591
Effective search space used:    87591
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 (21.7 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