Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_011390163.1 RRU_RS12480 homoserine dehydrogenase
Query= BRENDA::Q9WZ17 (739 letters) >NCBI__GCF_000013085.1:WP_011390163.1 Length = 430 Score = 188 bits (477), Expect = 6e-52 Identities = 142/418 (33%), Positives = 211/418 (50%), Gaps = 20/418 (4%) Query: 20 VRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGVPKEEIAFD 79 ++V +AGLGTVG + ++L + + + R G ++S V RS + GV A+ Sbjct: 5 LKVAVAGLGTVGAGVVKLLADHKDLLAARAGRPVVVSAVSARSRTRDR--GVDLSSYAW- 61 Query: 80 FDDLIL-----NSDVVVEAIGGTDVAVDLV-RRALELGRIVVTPNKNLISEYGNEFSEYI 133 FDD + +DVVVE IGG+D V AL+LGR VVT NK L++ +G + Sbjct: 62 FDDPVALVREAKADVVVELIGGSDGPAKAVCETALDLGRPVVTANKALLAHHGLALAARA 121 Query: 134 KKRK--LFFEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMSK-GRHFEEV 190 + L+FEA+V GGIPII L++ L ++ + GI+NGT NYILT M + GR F +V Sbjct: 122 EATGAGLWFEAAVAGGIPIIKALREGLAANRIDALHGILNGTCNYILTTMRESGRDFADV 181 Query: 191 LKEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEI 250 L EAQ LGYAEADP DI+G D A+K+++LA + + V +GI I ++ Sbjct: 182 LAEAQALGYAEADPGFDIDGIDAAHKLALLASLAFHVPVDLGGVSIQGIRHISSLDIRFA 241 Query: 251 VRSGKKLKLIGELDFSTNRYEVRLREV-TPED-PFFNVDGVDNAIEVSTDLAGDFLLKGR 308 G ++KL+ + E R+ V P D P +V+GV+NA+ D G + +GR Sbjct: 242 DELGYRIKLLAMARRTAEGVEQRVAPVMVPLDAPLAHVEGVNNAVVTEGDFVGRSVFQGR 301 Query: 309 GAGGYPTASAVIADLFRVAKYKVLGGAEKFSVVVMKFGGAAISDVEKLEKVAEKIIKRKK 368 GAG PTASAV+ADL +A+ K V + ++ + E + R Sbjct: 302 GAGAGPTASAVVADLIDLAR------GHKVPVFGVPSSALSVLPRAEPEDHVGRYYVRLM 355 Query: 369 SGVKPVVVLSAMGDTTDHLIELAKTIDENPDPRELDLLLSTGEIQSVALMSIALRKRG 426 +P V D + + + DP E ++ T A M+ AL + G Sbjct: 356 VVDRPGVFAEVAAALRDEQVSMESVLQRARDPGETVPVVMTLHDTGEAAMTRALARIG 413 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: 710 Number of extensions: 39 Number of successful extensions: 7 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: 430 Length adjustment: 36 Effective length of query: 703 Effective length of database: 394 Effective search space: 276982 Effective search space used: 276982 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