Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_013258203.1 DEBA_RS06900 homoserine dehydrogenase
Query= BRENDA::Q9WZ17 (739 letters) >NCBI__GCF_000143965.1:WP_013258203.1 Length = 435 Score = 204 bits (520), Expect = 6e-57 Identities = 139/418 (33%), Positives = 226/418 (54%), Gaps = 16/418 (3%) Query: 18 RKVRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGVPKEEIA 77 +++ VG+ GLGTVGG + R+L E+ + +G + +++ +R P + L +P + Sbjct: 4 KRINVGLIGLGTVGGGVARLLLEQQRRLSDYLGAELTLARAADRDPALAQGLDLPAGVLV 63 Query: 78 FDFDDLILNS--DVVVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYIKK 135 D ++ + D+VVE IGG + A V A+ G+ V T NK L++ +G E ++ Sbjct: 64 ADGAAVVADPQVDIVVELIGGLEPARAFVLAAIAGGKHVATANKALLAHHGREIFLAARQ 123 Query: 136 RKL--FFEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMS-KGRHFEEVLK 192 + + FEASVGGGIP+I L++ L ++ GI+NGT N+IL++M+ +G + +VL Sbjct: 124 KGVGVAFEASVGGGIPLIRSLREGLAANDISHCLGILNGTCNFILSKMTAEGAAYADVLA 183 Query: 193 EAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEIVR 252 +AQ+ GYAEADPT D+ G D A+K++++A +VTGR P +N + EGIT+I P ++ Sbjct: 184 QAQQEGYAEADPTFDVAGTDTAHKLAIIAALVTGRQPELNDISTEGITKIAPLDIQLAGE 243 Query: 253 SGKKLKLIGELDFSTNRYEVRLRE--VTPEDPFFNVDGVDNAIEVSTDLAGDFLLKGRGA 310 G K+KL+ L E+R+ V P +VDG NA+ V D G+ LL GRGA Sbjct: 244 FGFKVKLLAVLRKVGQAVELRVHPTLVPLGHPMASVDGPFNALFVEGDWVGEVLLYGRGA 303 Query: 311 GGYPTASAVIADLFRVAKYKVLGGAEKFSVVVMKFGGAAISD----VEKLEKVAEKIIKR 366 G PTASAV+ D+ +A+ + G + V G AA + + L++ K R Sbjct: 304 GRRPTASAVVGDVLDLARDVLCGCPGR----VPPLGSAAEPEGPLALAPLDQTVCKYYFR 359 Query: 367 KKSGVKPVVVLSAMGDTTDHLIELAKTIDE-NPDPRELDLLLSTGEIQSVALMSIALR 423 + KP V+ + +H I + I + + + +++ T E A+ R Sbjct: 360 FAAQDKPGVLAAISAVLAEHRISIEAVIQKGREEAGPVPIVMLTHEANEAAVQRALAR 417 Score = 27.7 bits (60), Expect = 0.001 Identities = 19/71 (26%), Positives = 35/71 (49%), Gaps = 15/71 (21%) Query: 607 DKPGVAARIMRTLSQMGVNIDMIIQGMKSGEYNTVAFIVPESQLGKLDIDLLKTRSEAKE 666 DKPGV A I L++ ++I+ +IQ + + G + I +L EA E Sbjct: 364 DKPGVLAAISAVLAEHRISIEAVIQKGR-------------EEAGPVPIVML--THEANE 408 Query: 667 IIIEKGLAKVS 677 +++ LA+++ Sbjct: 409 AAVQRALARIN 419 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: 655 Number of extensions: 39 Number of successful extensions: 6 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: 435 Length adjustment: 36 Effective length of query: 703 Effective length of database: 399 Effective search space: 280497 Effective search space used: 280497 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