Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_012973715.1 AZL_RS05775 homoserine dehydrogenase
Query= BRENDA::Q9WZ17 (739 letters) >NCBI__GCF_000010725.1:WP_012973715.1 Length = 434 Score = 193 bits (490), Expect = 2e-53 Identities = 129/320 (40%), Positives = 183/320 (57%), Gaps = 14/320 (4%) Query: 20 VRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGVPKEEIAFD 79 +++ +AGLGTVG + ++L + + IE+R G + + V RS K GV + + Sbjct: 9 LKIAVAGLGTVGAGVLKLLDTQASLIERRCGRRIEVVAVSARSKGKDR--GVDLSAVQW- 65 Query: 80 FDDLIL-----NSDVVVEAIGGTD-VAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYI 133 FDD + +D+VVE IGG++ A D V A+E G+ VVT NK L++ +G + Sbjct: 66 FDDPVAMAAQSGADLVVELIGGSEGPARDTVATAIETGKHVVTANKALLAVHGTGIARKA 125 Query: 134 KKRKLF--FEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEM-SKGRHFEEV 190 + L FEA+V GGIPII L++ L V+ I GI+NGT NYILTEM + GR F +V Sbjct: 126 EAGGLTVAFEAAVAGGIPIIKGLREGLAANGVSEIHGILNGTCNYILTEMRTTGRDFADV 185 Query: 191 LKEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEI 250 L +AQ LGYAEADP+ D++G D A+K+++LA V G SV EGI ++ Sbjct: 186 LADAQALGYAEADPSFDVDGIDAAHKLAILASVAFGTAVDFASVFIEGIRQVSAVDFDYA 245 Query: 251 VRSGKKLKLIGELDFSTNRYEVRLRE--VTPEDPFFNVDGVDNAIEVSTDLAGDFLLKGR 308 + G ++KL+G + E R+ V P +VDGV NA+ D A L GR Sbjct: 246 DQLGFRIKLLGIARRTDAGIEQRVHPCMVPKTAPIASVDGVFNAVVAQADFADRVLFVGR 305 Query: 309 GAGGYPTASAVIADLFRVAK 328 GAG PTASAV+ADL +A+ Sbjct: 306 GAGAGPTASAVVADLIDIAR 325 Score = 25.4 bits (54), Expect = 0.006 Identities = 11/31 (35%), Positives = 18/31 (58%) Query: 605 VPDKPGVAARIMRTLSQMGVNIDMIIQGMKS 635 V D+PGV A I + GV+++ +Q +S Sbjct: 360 VKDRPGVIADIAAAMRDQGVSMEQFLQRGRS 390 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: 708 Number of extensions: 41 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: 434 Length adjustment: 36 Effective length of query: 703 Effective length of database: 398 Effective search space: 279794 Effective search space used: 279794 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.
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:
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