Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_018231339.1 THITHI_RS0101700 homoserine dehydrogenase
Query= BRENDA::Q9WZ17 (739 letters) >NCBI__GCF_000378965.1:WP_018231339.1 Length = 436 Score = 206 bits (524), Expect = 2e-57 Identities = 150/408 (36%), Positives = 213/408 (52%), Gaps = 13/408 (3%) Query: 17 VRKVRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGVPKEEI 76 ++ V VG+ GLGTVG +L G+EI +R G + R ++ + + + Sbjct: 1 MKPVNVGLLGLGTVGCGAINVLARNGDEIARRAGRGIEVVAASARDLERPRECSLDRIRL 60 Query: 77 AFDFDDLILNSDV--VVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYIK 134 D D++ + V VVE IGGT A +LV A+E G+ VVT NK LI+ +GNE + Sbjct: 61 HADPFDVVNDPQVQIVVELIGGTSPARELVLAAIEQGKHVVTANKALIALHGNEIFAAAQ 120 Query: 135 KRKLF--FEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEM-SKGRHFEEVL 191 R + FEA+V GGIPII +++ L ++ + GI+NGT N+ILTEM KGR F +VL Sbjct: 121 ARGVMVAFEAAVAGGIPIIKAIREGLSGNRILWLAGIINGTGNFILTEMRDKGREFADVL 180 Query: 192 KEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEIV 251 EAQ LGYAEADPT D+EG D A+K+++LA + G + V EGI RI E + Sbjct: 181 AEAQRLGYAEADPTFDVEGIDAAHKLTILASIAFGIPLQFDKVYTEGIARITREDVAYAA 240 Query: 252 RSGKKLKLIGELDFSTNRYEVRLRE--VTPEDPFFNVDGVDNAIEVSTDLAGDFLLKGRG 309 G ++K +G S E+R+ + NVDGV NA+ V D G L G G Sbjct: 241 ELGYRIKHLGIARQSEQGIELRVHPTLIPHRRLIANVDGVMNAVLVMGDAVGPTLYYGAG 300 Query: 310 AGGYPTASAVIADLFRVAKYKVLGGAEKFSVVVMKFGGAAISD--VEKLEKVAEKIIKRK 367 AG PTASAV+ADL V + L + V + F A+SD V +E+V R Sbjct: 301 AGAEPTASAVVADLVDVV--RALTSDPENRVPHLAFQADALSDTAVLSMEEVQTAFYLRL 358 Query: 368 KSGVKPVVVLSAMGDTTDHLIELAKTIDENPD--PRELDLLLSTGEIQ 413 + +P V+ D I L + PD E ++L T +++ Sbjct: 359 RVQDRPGVLADITRILGDQDISLEAVLQREPDEAAAEASVILLTHKVR 406 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: 696 Number of extensions: 30 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: 436 Length adjustment: 36 Effective length of query: 703 Effective length of database: 400 Effective search space: 281200 Effective search space used: 281200 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