GapMind for Amino acid biosynthesis

 

Alignments for a candidate for asp-kinase in Denitrovibrio acetiphilus DSM 12809

Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_013010710.1 DACET_RS07130 homoserine dehydrogenase

Query= BRENDA::Q9WZ17
         (739 letters)



>NCBI__GCF_000025725.1:WP_013010710.1
          Length = 439

 Score =  182 bits (461), Expect = 4e-50
 Identities = 127/339 (37%), Positives = 183/339 (53%), Gaps = 19/339 (5%)

Query: 20  VRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRS---PQKYELLGVPKEEI 76
           V VG+ G GTVG     +L +  N I +  G    +  V + +       ELL +   E+
Sbjct: 5   VNVGLIGYGTVGKGTAEVLLKNKNLIFENTGIDIRLKTVADLAIDTANPDELLSLC--EV 62

Query: 77  AFDFDDLILNS---DVVVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEY- 132
             +  + ILN    D+VVE IGG   A D +  AL   + VV+ NK L + YG E  +  
Sbjct: 63  VTNNAEDILNDQDIDIVVELIGGYTFAKDFIISALNKKKHVVSANKALFAMYGTEIYQAA 122

Query: 133 -IKKRKLFFEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMSK-GRHFEEV 190
            +    + FE +VGGGIP++ ++++ L    +  I GI+NGT NYIL++M K G+ FEEV
Sbjct: 123 ELNNVSVCFEGAVGGGIPVLRVIKEDLAGNNINEIFGIINGTANYILSKMEKEGKEFEEV 182

Query: 191 LKEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGIT---RIDPEYL 247
           LK AQELGYAEADPT DIEG D A+K+++LA +          +  EGIT   +ID E+ 
Sbjct: 183 LKVAQELGYAEADPTFDIEGIDSAHKIAILASMAFNTLIPFEKIYVEGITSIKQIDIEFA 242

Query: 248 KEIVRSGKKLKLIGELDFSTNRYEVRLREVTPEDP--FFNVDGVDNAIEVSTDLAGDFLL 305
           K++     K+KL+       N  EVR+      D      VDGV NA+E+  D++   + 
Sbjct: 243 KKL---DCKIKLLAIAKKHENDLEVRVHPTMVPDVELMAQVDGVFNAVEIIGDMSDKTMH 299

Query: 306 KGRGAGGYPTASAVIADLFRVAKYKVLGGAEKFSVVVMK 344
            GRGAGG PT SAV  D+  +A+    G  ++  ++  K
Sbjct: 300 YGRGAGGKPTGSAVAGDVISIARDIAAGCTKRTPILGFK 338


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: 774
Number of extensions: 49
Number of successful extensions: 6
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: 739
Length of database: 439
Length adjustment: 36
Effective length of query: 703
Effective length of database: 403
Effective search space:   283309
Effective search space used:   283309
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 Jul 25 2024. The underlying query database was built on Jul 25 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