GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Dyella japonica UNC79MFTsu3.2

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 N515DRAFT_0565 N515DRAFT_0565 threonine dehydratase

Query= SwissProt::Q7XSN8
         (339 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0565
          Length = 523

 Score =  173 bits (439), Expect = 8e-48
 Identities = 106/311 (34%), Positives = 175/311 (56%), Gaps = 12/311 (3%)

Query: 25  REAQARIAPYVHKTPVLSSTSIDAIVGKQLFFKCECFQKAGAFKIRGASNSIFALDDDEA 84
           R   AR+     +T + S+  + A +G+++  K E  Q   +FK+RGA N +  LD  + 
Sbjct: 21  RTLAARVYEVARETALESAPLLSARLGQRVLLKREDQQPVFSFKLRGAYNKMVGLDAAQR 80

Query: 85  SKGVVTHSSGNHAAAVALAAKLRGIPAYIVIPRNAPACKVDNVKRYGG---HIIWSDVSI 141
           ++GV+  S+GNHA  VALAA   G+ A IV+P  AP  K+D V+R GG    ++ +  S 
Sbjct: 81  ARGVIAASAGNHAQGVALAAAKLGLRAVIVMPVTAPQVKIDAVRRLGGAWVEVVLAGDSY 140

Query: 142 ESRESVAKRVQEETGAILVHPFNNKNTISGQGTVSLELLEEVP-EIDTIIVPISGGGLIS 200
              ++ A R++++ G   VHPF++   I+GQ TV +E+L + P  +  + VP+ GGGL++
Sbjct: 141 SDAQAEAARLEQQHGYTFVHPFDDPAVIAGQATVGMEILRQHPGPLHAVFVPVGGGGLLA 200

Query: 201 GVALAAKAINPSIRILAAEPKGADDSAQSKAAGKIITLPSTNTIADGLRA-FLGDLTWPV 259
           GVA   KA+ P ++++  +   +D  AQS   G+ +TL      ADG     +G  T+ +
Sbjct: 201 GVAAYIKALRPEVKVIGVQTVDSDAMAQSLEQGERVTLDEVGLFADGTAVKRVGAETFAL 260

Query: 260 VRDLVDDIIVVDDNAIVDAMKMCYEMLKVAVEPSGAIGLAAALSDEFKQSSAWH--ESSK 317
            +  VD ++ VD +AI  A++  ++  +   EPSGA+ LA       KQ +A H  + + 
Sbjct: 261 CQRHVDAMLRVDTDAICAAIRDVFQETRSVPEPSGALALAG-----LKQYAATHQLDDAT 315

Query: 318 IGIIVSGGNVD 328
           +  IVSG N++
Sbjct: 316 LVAIVSGANLN 326


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: 329
Number of extensions: 17
Number of successful extensions: 4
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: 523
Length adjustment: 32
Effective length of query: 307
Effective length of database: 491
Effective search space:   150737
Effective search space used:   150737
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: 50 (23.9 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