GapMind for Amino acid biosynthesis

 

Alignments for a candidate for asp-kinase in Sinorhizobium fredii NGR234

Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate YP_002825934.1 NGR_c14020 homoserine dehydrogenase

Query= BRENDA::Q9WZ17
         (739 letters)



>NCBI__GCF_000018545.1:YP_002825934.1
          Length = 440

 Score =  202 bits (514), Expect = 3e-56
 Identities = 133/319 (41%), Positives = 186/319 (58%), Gaps = 12/319 (3%)

Query: 20  VRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGVPKEEIAFD 79
           +++GIAGLGTVG S+ RIL+ER   +    G    +  V  R   K    GV   + A+ 
Sbjct: 5   LKIGIAGLGTVGASLVRILQERHEMLATTCGRPIELVAVAARDRSKDR--GVDLAKAAWF 62

Query: 80  FDDLILNS----DVVVEAIGGT-DVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYIK 134
            D + L S    DV VE +GG  D A   V+ AL+ G  VVT NK L++++G E +   +
Sbjct: 63  EDAVALASEADIDVFVELMGGAGDPAYSSVKAALKRGIHVVTANKALLAKHGIELAAIAE 122

Query: 135 KRK--LFFEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMSK-GRHFEEVL 191
           ++   L +EA+V GGIP+I  L++ L    V+R+ GIMNGT NYILT+M + G  FE  L
Sbjct: 123 EQGALLNYEAAVAGGIPVIKALRESLTGNTVSRVYGIMNGTCNYILTKMEREGLTFEACL 182

Query: 192 KEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEIV 251
           KEAQ LGYAEADP  DIEG D A+K+S+L  +  G     + +  EGIT I  E ++   
Sbjct: 183 KEAQRLGYAEADPAFDIEGNDTAHKLSILTSLAFGTAIAADDIYLEGITNISIEDIQAAA 242

Query: 252 RSGKKLKLIGELDFSTNRYEVRLR-EVTPEDPFF-NVDGVDNAIEVSTDLAGDFLLKGRG 309
             G ++KL+G    + +  E R+   + P D     VDGV NA+ V +D+ G+ L+ G G
Sbjct: 243 DLGYRIKLLGVAQRTESGIEQRVHPTMVPYDSVIAQVDGVTNAVAVESDILGELLMVGPG 302

Query: 310 AGGYPTASAVIADLFRVAK 328
           AGG  TASAV+ D+  +AK
Sbjct: 303 AGGNATASAVLGDIADIAK 321


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: 699
Number of extensions: 34
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: 739
Length of database: 440
Length adjustment: 36
Effective length of query: 703
Effective length of database: 404
Effective search space:   284012
Effective search space used:   284012
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