Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_011766840.1 AZO_RS15630 aspartate kinase
Query= BRENDA::Q9WZ17 (739 letters) >NCBI__GCF_000061505.1:WP_011766840.1 Length = 408 Score = 324 bits (831), Expect = 5e-93 Identities = 179/405 (44%), Positives = 266/405 (65%), Gaps = 5/405 (1%) Query: 339 SVVVMKFGGAAISDVEKLEKVAEKIIKRKKSGVKPVVVLSAMGDTTDHLIELAKTIDENP 398 +++V K+GG ++ E+++ VA K+ K + G + VVV+SAM T+ LI LAK + P Sbjct: 2 ALIVQKYGGTSVGSPERIKNVASKVAKFRAEGHQVVVVVSAMSGETNRLIALAKDVAAKP 61 Query: 399 DPRELDLLLSTGEIQSVALMSIALRKRGYKAISFTGNQLKIITDKRYGSARIIDINTDII 458 DPRELD+++STGE ++ L+ +AL+ G A S+TG Q+KI+TD + ARI++I+ I Sbjct: 62 DPRELDVVVSTGEQVTIGLLCMALQDIGVPAKSYTGAQVKILTDSAHTKARILNIDEAPI 121 Query: 459 SRYLKQDFIPVVAGFQGITETGDITTLGRGGSDLTAIALAYSLGADLCELYKDVDGVYTA 518 + L + VVAGFQG+ E G+ITTLGRGGSD T +ALA +L AD C++Y DVDGVYT Sbjct: 122 RKDLDAGAVVVVAGFQGVDEHGNITTLGRGGSDTTGVALAAALKADECQIYTDVDGVYTT 181 Query: 519 DPRIVKDARVIKELSWEEMIELSRHGAQVLQARAAEFARKYGVKVLIKNAHKE-TRGTLI 577 DPRIV +AR + +++EEM+E++ G++VLQ R+ EFA KY VK+ + ++ +E +GTLI Sbjct: 182 DPRIVPEARKLDTITFEEMLEMASLGSKVLQIRSVEFAGKYKVKLRVLSSFQEGGQGTLI 241 Query: 578 W--EGTKVENPIVRAVTFEDGMAKVVLKDVPDKPGVAARIMRTLSQMGVNIDMIIQGMKS 635 E +E P++ + F AKV + VPDKPG+A +I+ ++ +++DMIIQ + Sbjct: 242 TVEEDKNMEQPVISGIAFNRDEAKVTVLGVPDKPGIAYQILGPVADANLDVDMIIQNVGH 301 Query: 636 GEYNTVAFIVPESQLGK--LDIDLLKTRSEAKEIIIEKGLAKVSIVGVNLTSTPEISATL 693 +F + L K ++ +KT A+ I +K + KVSIVGV + S P +++ + Sbjct: 302 DGTTDFSFTLARGDLEKAVAILEGVKTHIGARAIEGDKTMCKVSIVGVGMRSHPGVASKM 361 Query: 694 FETLANEGINIDMISASSSRISVIIDGKYVEDAVKAIHSRFELDR 738 F TLA EGINI MIS S +ISV ID KY+E AV+ +H F LD+ Sbjct: 362 FRTLAEEGINIQMISTSEIKISVAIDEKYLELAVRVLHKAFGLDQ 406 Score = 27.3 bits (59), Expect = 0.002 Identities = 23/74 (31%), Positives = 35/74 (47%), Gaps = 8/74 (10%) Query: 44 EIEKRIGEKFIISKVINRSPQKYELLGVP-KEEIAFDF----DDLILNSDVVVEAI---G 95 E +K + + I NR K +LGVP K IA+ D L+ D++++ + G Sbjct: 244 EEDKNMEQPVISGIAFNRDEAKVTVLGVPDKPGIAYQILGPVADANLDVDMIIQNVGHDG 303 Query: 96 GTDVAVDLVRRALE 109 TD + L R LE Sbjct: 304 TTDFSFTLARGDLE 317 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: 737 Number of extensions: 37 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 739 Length of database: 408 Length adjustment: 36 Effective length of query: 703 Effective length of database: 372 Effective search space: 261516 Effective search space used: 261516 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