GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Stenotrophomonas chelatiphaga DSM 21508

Align L-threonine dehydratase catabolic TdcB; L-serine dehydratase; Threonine deaminase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate WP_057509300.1 ABB28_RS14485 threonine dehydratase

Query= SwissProt::P11954
         (329 letters)



>NCBI__GCF_001431535.1:WP_057509300.1
          Length = 366

 Score =  211 bits (537), Expect = 2e-59
 Identities = 123/310 (39%), Positives = 180/310 (58%), Gaps = 17/310 (5%)

Query: 9   VAIEDILEAKKRLAGKIYKTGMPRSNYFSERCKGEIFLKFENMQRTGSFKIRGAFNKLSS 68
           V + D+L A+ RL   +  T +  +  F        +LK EN+QRTGS+K+RGA N L +
Sbjct: 16  VTVADVLAAQARLRRFLPPTPLHHAERFGT------WLKLENLQRTGSYKVRGALNALLA 69

Query: 69  LTEAEKRKGVVACSAGNHAQGVSLSCAMLGIDGKVVMPKGAPKSKVAATCDYSAEVVLHG 128
             E    + ++  SAGNHAQGV+ +   LG+    VMP GAP +K+A    + A V  HG
Sbjct: 70  GRERGDLRPIICASAGNHAQGVAWAAHRLGVQAITVMPHGAPANKIAGVAHWGATVRQHG 129

Query: 129 DNFNDTIAKVSEIVETEGRIFIPPYDDPKVIAGQGTIGLEIMEDLYDVDNVIVPIGGGGL 188
           ++++D  A   E+ +     F+  +DD  VIAGQGT+G+E+     DV  VIVPIGGGGL
Sbjct: 130 ESYDDAWAFAVELAQRHDYRFLSAFDDADVIAGQGTVGIELAPHSPDV--VIVPIGGGGL 187

Query: 189 IAGIAIAIKSINPTIKVIGVQAENVHGMAASYYTGEITTHRTTGTLADGCDVSRPGNLTY 248
            +G+A+A+KS    ++++G Q E V  MA +  +G+I       +LADG  V  PG LT 
Sbjct: 188 ASGVALALKS--QGVRIVGAQVEGVDSMARA-ISGDIRPIAPVPSLADGVRVKIPGFLTR 244

Query: 249 EIVRELVDDIVLVSEDEIRNSMIALIQRNKVITEGAGALACAALLSGKLDSHIQNRKTVS 308
            +   L+DD+V+V E E+R +++ L     +I EGAGALA AA         +  R+  +
Sbjct: 245 RLCASLLDDVVIVREAELRETLVRLALEENLIAEGAGALALAA------GRRVAGRRKFA 298

Query: 309 IISGGNIDLS 318
           ++SGGNID S
Sbjct: 299 VVSGGNIDAS 308


Lambda     K      H
   0.317    0.136    0.382 

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: 247
Number of extensions: 7
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: 366
Length adjustment: 29
Effective length of query: 300
Effective length of database: 337
Effective search space:   101100
Effective search space used:   101100
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: 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