GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Stenotrophomonas chelatiphaga DSM 21508

Align D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate WP_057509300.1 ABB28_RS14485 threonine dehydratase

Query= BRENDA::Q54HH2
         (324 letters)



>NCBI__GCF_001431535.1:WP_057509300.1
          Length = 366

 Score =  142 bits (358), Expect = 1e-38
 Identities = 96/318 (30%), Positives = 168/318 (52%), Gaps = 20/318 (6%)

Query: 7   VTLKDIKEAHKRIEKYIHKTPVLTNSTINELAGKELYFKCENLQKTGSFKMRGACNAIFS 66
           VT+ D+  A  R+ +++  TP      ++       + K ENLQ+TGS+K+RGA NA+ +
Sbjct: 16  VTVADVLAAQARLRRFLPPTP------LHHAERFGTWLKLENLQRTGSYKVRGALNALLA 69

Query: 67  LDEEELSKGVVTHSSGNHGQALSYASKVRCVKCYVVVPEDAPSVKLNAICGYGATVTKCK 126
             E    + ++  S+GNH Q +++A+    V+   V+P  AP+ K+  +  +GATV +  
Sbjct: 70  GRERGDLRPIICASAGNHAQGVAWAAHRLGVQAITVMPHGAPANKIAGVAHWGATVRQHG 129

Query: 127 ATLEARESNTKQLIEQHSCKLIHPFDNLQVIAGQGTASLELMEQVENLDAIITPVGGGGL 186
            + +   +   +L ++H  + +  FD+  VIAGQGT  +EL     + D +I P+GGGGL
Sbjct: 130 ESYDDAWAFAVELAQRHDYRFLSAFDDADVIAGQGTVGIELAP--HSPDVVIVPIGGGGL 187

Query: 187 LSGTCITAKSLNPNIKVFAAEPLGADDTYRSLLSGEIQKHTPGKPNTIADGLLTTV-GSL 245
            SG  +  KS    +++  A+  G D   R+ +SG+I+   P    ++ADG+   + G L
Sbjct: 188 ASGVALALKS--QGVRIVGAQVEGVDSMARA-ISGDIRPIAP--VPSLADGVRVKIPGFL 242

Query: 246 TFPIIKENCDGVILVTEDEIKYAMKLVWERMKIIIEPSSATTLAAILKQEFKDKKDIKKV 305
           T  +     D V++V E E++  +  +     +I E + A  LAA  +   + K      
Sbjct: 243 TRRLCASLLDDVVIVREAELRETLVRLALEENLIAEGAGALALAAGRRVAGRRK------ 296

Query: 306 GIIISGGNVDLSSISKIL 323
             ++SGGN+D S ++ +L
Sbjct: 297 FAVVSGGNIDASVLAGLL 314


Lambda     K      H
   0.315    0.132    0.374 

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: 236
Number of extensions: 9
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: 324
Length of database: 366
Length adjustment: 29
Effective length of query: 295
Effective length of database: 337
Effective search space:    99415
Effective search space used:    99415
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 (21.5 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