Align homoserine dehydrogenase (EC 1.1.1.3) (characterized)
to candidate WP_010964316.1 CA_RS05310 homoserine dehydrogenase
Query= BRENDA::P19582 (433 letters) >NCBI__GCF_000008765.1:WP_010964316.1 Length = 429 Score = 352 bits (903), Expect = e-101 Identities = 173/430 (40%), Positives = 284/430 (66%), Gaps = 6/430 (1%) Query: 1 MKAIRVGLLGLGTVGSGVVKIIQDHQDKLMHQVGCPVTIKKVLVKDLEKKREVDLPKEVL 60 M I++G+LGLG VG GV+KI+ +++++ + G + I K+LV++++K R +D+P+E+L Sbjct: 1 MDKIKIGILGLGNVGRGVLKILNTNKEEIQKRSGYDIEIGKILVRNIDKNRGIDVPRELL 60 Query: 61 TTEVYDVIDDPDVDVVIEVIGGVEQTKQYLVDALRSKKHVVTANKDLMAVYGSELLAEAK 120 T + D+++D + +VIEVIGG+ K Y++ A+++KKHVVTANK L+A G EL A+ Sbjct: 61 TVDPDDILEDESIKIVIEVIGGINPAKDYILRAMKNKKHVVTANKMLLATEGDELFDTAE 120 Query: 121 ENGCDIYFEASVAGGIPILRTLEEGLSSDRITKMMGIVNGTTNFILTKMIKEKSPYEEVL 180 E G Y+EASVAGGIPI+ + E L++++I +++GI+NGTTN+ILTKM EK + + L Sbjct: 121 EEGVMFYYEASVAGGIPIIHAINESLTANKIEQLIGIINGTTNYILTKMTLEKMNFHDAL 180 Query: 181 KEAQDLGFAEADPTSDVEGLDAARKMAILARLGFSMNVDLEDVKVKGISQITDEDISFSK 240 +EAQ+ GFAEADPTSD+E DA K+AIL+ L F ++++DV +GI++I DI F++ Sbjct: 181 REAQEKGFAEADPTSDIEAYDAMYKLAILSSLSFGTKINVDDVYREGITKIEPIDIEFAR 240 Query: 241 RLGYTMKLIGIAQRDGSKIEVSVQPTLLPDHHPLSAVHNEFNAVYVYGEAVGETMFYGPG 300 GY +KL+ I + + +E+ V PT++P+ HPL+ V++ FNA+++ G AVG+ M YG G Sbjct: 241 EFGYVIKLVAIVKETETGLEMRVHPTMIPERHPLANVNDSFNAIFIKGNAVGDIMLYGRG 300 Query: 301 AGSMPTATSVVSDLVAVMKNMRLGVTGNSFVGPQYEKNMKSPSD-IYAQQFLRIHVKDEV 359 AG +PT ++VV+D++++++ + ++ S V Y +P D ++ ++RI VKD Sbjct: 301 AGDLPTGSAVVADVISILRG-NVDLSAISTVKKNYWNREINPMDKTRSEYYVRITVKDLP 359 Query: 360 GSFSKITSVFSERGVSFEKILQLPIKG-HDELAEIVIVTHHTSEADFSDILQNLNDLEVV 418 G +I+ +F E GVS ++Q KG +E +V TH +E + + + Sbjct: 360 GVLGEISMIFGEEGVSLLSVMQ---KGKREECVTVVYFTHSANEGMIKSAIDRIKSSKYT 416 Query: 419 QEVKSTYRVE 428 + V + R+E Sbjct: 417 KSVDNIIRIE 426 Lambda K H 0.316 0.135 0.372 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: 421 Number of extensions: 15 Number of successful extensions: 3 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: 433 Length of database: 429 Length adjustment: 32 Effective length of query: 401 Effective length of database: 397 Effective search space: 159197 Effective search space used: 159197 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 (21.6 bits) S2: 51 (24.3 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