Align homoserine dehydrogenase (EC 1.1.1.3) (characterized)
to candidate WP_013643891.1 METBO_RS01460 homoserine dehydrogenase
Query= BRENDA::D8WXQ1 (432 letters) >NCBI__GCF_000191585.1:WP_013643891.1 Length = 426 Score = 333 bits (855), Expect = 5e-96 Identities = 180/420 (42%), Positives = 270/420 (64%), Gaps = 6/420 (1%) Query: 2 EAIQVGLLGLGTVGSGVVKIIENHQDKLMHQVGCPVKVKKILVQDLNKKRDVDVDPAQLT 61 + + +GL+G GT+GSGVV+ + + D + ++VG VK+KK++ D+ R V++ L+ Sbjct: 3 DTVNIGLIGFGTIGSGVVETLNKNIDLVENKVGKKVKLKKVVDLDITTDRGVEISSDVLS 62 Query: 62 TNADDILQDPDIDVVIEVMGGIEETRNYLLKALSEKKHVVTANKDLMAVYGSELLTAASA 121 T+ +DIL DPDI++VIE+MGG + ++ KA+ KHVVTANK L+A + E+++ A Sbjct: 63 TDINDILDDPDIEIVIELMGGYQPALKFITKAMENGKHVVTANKALLAKHWDEIISTAQK 122 Query: 122 NGCDLFYEASVAGGIPILRSLVDGLASDRITKMMGIVNGTTNYILTKMSKHGRAYEEVLK 181 N + +EASV GGIP+L+ L +GL+++ I + GI+NGT NYILTKM+ G +E+VLK Sbjct: 123 NDVRICFEASVGGGIPLLQPLNEGLSANNIQSIYGIINGTANYILTKMTDEGLEFEDVLK 182 Query: 182 EAQELGYAEADPASDVEGLDAARKMAILATLGFSMKIDLDDVKVEGITRITEEDIQYGK- 240 EAQ+ GYAEADP+ D+EG D A+K+ IL L F I D+ VEGIT IT EDI + K Sbjct: 183 EAQKKGYAEADPSFDIEGDDTAQKLIILTILSFGKYIKQDNFHVEGITCITPEDISFAKE 242 Query: 241 QLGYTMKLIGIAHREGEKVEVSVQPTLLSDSHPLASVNDEYNAVYVYGEAVGETMFYGPG 300 +L +KL+ IA K+EV V PT++ H L+SVN +N VY+ G+ VG M YGPG Sbjct: 243 ELNSCIKLLAIAKLVDGKLEVRVHPTIVPLDHLLSSVNGVFNGVYLVGDVVGPVMMYGPG 302 Query: 301 AGSLPTATAVVSDLVGVMKNMRLGV-NGANAVTPQYQKKLKGPDEIYSKFFLRLHVKDEV 359 AG +PTA+AVV D + +++NM V G + T + K+K ++ SK++LRL KDE Sbjct: 303 AGMMPTASAVVGDCIDIIENMEKPVLYGPKSCTVE---KIKDISDLESKYYLRLITKDEP 359 Query: 360 GVFANITSIFSEHSVSFEKILQMPLKENGLAEIVLVTHQASLQDYEDILVKLRDLNAVHE 419 GV I+ I S++++S + Q + G+ I +VTH A +D + ++ L V++ Sbjct: 360 GVLHKISGILSKYNISIGSMTQKQHDKPGI-PIFMVTHSALERDMRSAVEEIDQLKCVND 418 Lambda K H 0.316 0.134 0.368 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: 523 Number of extensions: 31 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: 432 Length of database: 426 Length adjustment: 32 Effective length of query: 400 Effective length of database: 394 Effective search space: 157600 Effective search space used: 157600 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