GapMind for Amino acid biosynthesis

 

Alignments for a candidate for asp-kinase in Halomonas desiderata SP1

Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_086508980.1 BZY95_RS05570 homoserine dehydrogenase

Query= BRENDA::Q9WZ17
         (739 letters)



>NCBI__GCF_002151265.1:WP_086508980.1
          Length = 438

 Score =  207 bits (528), Expect = 7e-58
 Identities = 132/321 (41%), Positives = 188/321 (58%), Gaps = 13/321 (4%)

Query: 17  VRKVRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQ-KYELLGVPKEE 75
           ++ VRVGI GLGTVGG  + +L    +EI +R G   +I +V  RS   + +L G+    
Sbjct: 1   MKPVRVGICGLGTVGGGTFNVLTRNADEIARRAGRPIVIEQVALRSTNPECDLTGIKTTN 60

Query: 76  IAFDF---DDLILNSDVVVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEY 132
             F+     D+    DV+VE +GG DV  +LV  A+  G+ VVT NK LI+ +GNE  + 
Sbjct: 61  DVFEVARNPDI----DVLVEVLGGYDVPRELVLTAIANGKHVVTANKALIAVHGNEIFQA 116

Query: 133 IKKRKLF--FEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEM-SKGRHFEE 189
             ++ +   FEA+V GGIP+I  L++ L   ++  + GI+NGT NYILT M S+GR FE+
Sbjct: 117 AHEQGVIVAFEAAVAGGIPVIKSLREGLGANRIEWVAGIINGTGNYILTHMRSEGRAFED 176

Query: 190 VLKEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKE 249
           VL EAQ LGYAEADPT D+EG D A+K+++LA +  G          EGI+R+  + +++
Sbjct: 177 VLAEAQALGYAEADPTFDVEGIDAAHKLTILASIAYGVPLQFEKAYTEGISRVTFDDVEQ 236

Query: 250 IVRSGKKLKLIGELDFSTNRYEVRLRE--VTPEDPFFNVDGVDNAIEVSTDLAGDFLLKG 307
               G  +K +G    + +  E+R+    +  E    NV GV NAI +  D  G  L  G
Sbjct: 237 ADNLGYVIKHLGISKRTEHGLELRVHPTLIPKERLLANVHGVKNAIAIMGDAVGPTLYYG 296

Query: 308 RGAGGYPTASAVIADLFRVAK 328
            GAG  PTASAV+ADL  VA+
Sbjct: 297 AGAGSEPTASAVVADLLDVAR 317



 Score = 30.8 bits (68), Expect = 2e-04
 Identities = 11/25 (44%), Positives = 19/25 (76%)

Query: 607 DKPGVAARIMRTLSQMGVNIDMIIQ 631
           D+PGV AR+   LS+ G++I+ ++Q
Sbjct: 362 DRPGVLARVATILSEQGISIEALVQ 386


Lambda     K      H
   0.318    0.137    0.377 

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: 758
Number of extensions: 35
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 739
Length of database: 438
Length adjustment: 36
Effective length of query: 703
Effective length of database: 402
Effective search space:   282606
Effective search space used:   282606
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: 53 (25.0 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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