GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Cereibacter sphaeroides ATCC 17029

Align Serine racemase; D-serine ammonia-lyase; D-serine dehydratase; L-serine ammonia-lyase; L-serine dehydratase; EC 4.3.1.17; EC 4.3.1.18; EC 5.1.1.18 (characterized)
to candidate WP_011840691.1 RSPH17029_RS04715 threonine/serine dehydratase

Query= SwissProt::Q7XSN8
         (339 letters)



>NCBI__GCF_000015985.1:WP_011840691.1
          Length = 325

 Score =  206 bits (525), Expect = 5e-58
 Identities = 118/316 (37%), Positives = 184/316 (58%), Gaps = 11/316 (3%)

Query: 19  ADIHSIREAQARIAPYVHKTPVLSSTSIDAIVGKQLFFKCECFQKAGAFKIRGASNSIFA 78
           +DI  I  A AR+A +  +TP+LSS  +D I G+++  K EC Q  G+FK RG  +++ A
Sbjct: 2   SDIAMIEAAAARLAGHARRTPLLSSPFLDEIAGRRVLVKAECLQHTGSFKFRGGWSALSA 61

Query: 79  LDDDEASKGVVTHSSGNHAAAVALAAKLRGIPAYIVIPRNAPACKVDNVKRYGGHIIWSD 138
           L+    ++GV+ +SSGNHA  VALAA   G PA IV+P +AP  K++N +  G  ++  D
Sbjct: 62  LEPARRAQGVIAYSSGNHAQGVALAAARHGAPAVIVMPADAPQLKIENTRALGAEVVLYD 121

Query: 139 VSIESRESVAKRVQEETGAILVHPFNNKNTISGQGTVSLELLEEVPEIDT----IIVPIS 194
            + E R+++  R+ +E G  L+ PF+    I+GQGT  LE+ E+  E       ++    
Sbjct: 122 RATEDRDAIGARLADERGLTLIRPFDEPLVIAGQGTTGLEIAEQAAEEGVTSADVLTCCG 181

Query: 195 GGGLISGVALAAKAINPSIRILAAEPKGADDSAQSKAAGKIITLPS-TNTIADGL-RAFL 252
           GGGL +G+ALA +A  P +R+   EP G DD+A+S AAG+I +  + + +I D +     
Sbjct: 182 GGGLTAGIALALEARAPGLRVRPVEPVGFDDTARSLAAGEIRSNAALSGSICDAIVTPQP 241

Query: 253 GDLTWPVVRDLVDDIIVVDDNAIVDAMKMCYEMLKVAVEPSGAIGLAAALSDEFKQSSAW 312
           G +T+P++  L    + V D   + AM + +  LK+ +EP GA+ LAAAL   F+  +  
Sbjct: 242 GRITFPILARLCGPGLAVTDAEALRAMALAFLRLKIVLEPGGAVALAAAL---FRPEAL- 297

Query: 313 HESSKIGIIVSGGNVD 328
            +   +    SGGNVD
Sbjct: 298 -DGDAVICTASGGNVD 312


Lambda     K      H
   0.316    0.133    0.381 

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: 230
Number of extensions: 11
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: 339
Length of database: 325
Length adjustment: 28
Effective length of query: 311
Effective length of database: 297
Effective search space:    92367
Effective search space used:    92367
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 Apr 10 2024. 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