Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_018125378.1 B149_RS0111850 homoserine dehydrogenase
Query= BRENDA::Q9WZ17 (739 letters) >NCBI__GCF_000375485.1:WP_018125378.1 Length = 436 Score = 209 bits (532), Expect = 2e-58 Identities = 142/397 (35%), Positives = 210/397 (52%), Gaps = 11/397 (2%) Query: 17 VRKVRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGV-PKEE 75 ++ V++G+AG GTVG + IL+E G IE+RIG + I+ V+ R K P E Sbjct: 1 MKSVKLGLAGFGTVGSGLAAILEENGEWIERRIGRRLEIATVVVRDLNKPRAAATAPGTE 60 Query: 76 IAFDFDDLILNS--DVVVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYI 133 D L + D+VVE +GG D A DL+R ALE G+ VVT NK+L++E G E Sbjct: 61 FTTDLTRLTTDPEIDIVVECMGGLDSAYDLIRSALEAGKHVVTANKHLLAERGPELFAIA 120 Query: 134 KKRK--LFFEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMS-KGRHFEEV 190 ++ L FEAS GGIPI+ L++ L +V + GI+NGT NYIL+EM+ KG F Sbjct: 121 RENGTGLSFEASCAGGIPIVQTLKNSLAGDRVLEMLGILNGTANYILSEMTTKGMDFATA 180 Query: 191 LKEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEI 250 L +AQ+LGYAEADPT D+EG+D A+K+ VL+ + G ++ + +GIT + P ++ Sbjct: 181 LSKAQDLGYAEADPTFDVEGFDAAHKLCVLSRLAFGLDYPLSELPIQGITAVTPLDIELA 240 Query: 251 VRSGKKLKLIGELDFSTNRYEVRLREVTPEDPFF--NVDGVDNAIEVSTDLAGDFLLKGR 308 G ++KL+ + E + + F V G NA+ V + G +L G+ Sbjct: 241 REFGYRIKLMAHARVVDGKIEAGVHPALVKYTFLLARVGGNYNAVRVVGNAVGPVMLHGQ 300 Query: 309 GAGGYPTASAVIADLFRVAKYKVLGGA-EKFSVVVMKFGGAAISDVEKL--EKVAEKIIK 365 GAG PT SAV+AD+ +AK+ G E + F A I E L E+ Sbjct: 301 GAGDTPTGSAVLADIIDLAKHIDRSGCDEAYRPDNTGFRNADIPLAEILPPEESRSSYYF 360 Query: 366 RKKSGVKPVVVLSAMGDTTDHLIELAKTIDENPDPRE 402 R +P V+ + DH I +A+ + + + E Sbjct: 361 RFTVADRPGVMAAISKSMADHSISIAQAVQKGDEQSE 397 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: 745 Number of extensions: 37 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