Align homoserine dehydrogenase (EC 1.1.1.3) (characterized)
to candidate WP_027178114.1 G496_RS0103810 homoserine dehydrogenase
Query= reanno::Miya:8500664 (436 letters) >NCBI__GCF_000429985.1:WP_027178114.1 Length = 427 Score = 473 bits (1217), Expect = e-138 Identities = 242/422 (57%), Positives = 315/422 (74%), Gaps = 1/422 (0%) Query: 15 IGMAGFGTVGSGLARVLDENRQWITERTGREMVIKTILVRDLAKPRAWPVPQGATLTADP 74 + +AGFGTVG+G+AR+L+EN + + +R+G + VI ++LVRD K R + T +P Sbjct: 6 LALAGFGTVGTGVARILEENEELLLKRSGIKYVITSVLVRDTEKQRDYIPGPETKFTTNP 65 Query: 75 AVLTDDPEIDVLVELMGGIAAPHAIIKRALEAGKHVVTANKALLAEDGYDLYRLAEQKNV 134 LT DPE+DV+VELMGGI I+ +A+++GKHVVTANK LLA G +L++LAE+ V Sbjct: 66 EDLTADPEVDVVVELMGGITLAKEIVVKAIKSGKHVVTANKHLLAVHGIELFKLAEEYGV 125 Query: 135 GLHHEASVAGGIPIVQTLKESLAGNRIGSLVGILNGTANYILSEMTSNGLDFATALAQAQ 194 GL++EASVAGGIPIV+++KESL N+I ++VGILNGTANYILSEMT+NGL+F TAL+QAQ Sbjct: 126 GLYYEASVAGGIPIVESIKESLCVNKIKNIVGILNGTANYILSEMTTNGLEFDTALSQAQ 185 Query: 195 ELGYAEADPTLDIEGHDTAHKLVLLIRLAYGMDYPYAELPVQGIAGIDRMDIEFARELGF 254 ELGYAEADPT DIEG D AHKLV+LIRLAYG DYP ELPV+GI+ I +DI+ ARE G+ Sbjct: 186 ELGYAEADPTFDIEGIDAAHKLVVLIRLAYGEDYPLEELPVEGISKITGLDIKLAREFGY 245 Query: 255 RIKLLAQVREVDGKLEAGVFPTLVKHTFLIARVGGAYNAIRLEGNAVGPVFLHGLGAGSL 314 RIKL+ QVR+V GKLEAG+FP LVK+T L+ARVGG YNAIR+EGNAVGP F HG GAG+L Sbjct: 246 RIKLIGQVRDVCGKLEAGIFPALVKYTLLLARVGGNYNAIRVEGNAVGPAFFHGQGAGAL 305 Query: 315 PTASAVLADLMTVARGAAPHNTGFQRQVPPRADILPPADAESSYYVRAMVPDNPGVLRDL 374 PT SAV+AD+MT+ + P+NTGF +ADILPP A S YY R V D GV+ + Sbjct: 306 PTGSAVVADIMTLTKMDKPNNTGFYSSDLKKADILPPEHATSEYYFRFTVADKAGVMAAI 365 Query: 375 AGAMADHSISIAQAIQKGQ-HPQGVPLVFMTHAAKASAIQGAIAQVQAAGLLLAPPVCYR 433 + +++H+ISIAQA+QKG VP+VF+TH A+A + A+ + + + R Sbjct: 366 SKILSEHNISIAQAVQKGDASGVNVPIVFLTHKARAKDVNDALKIIDDMPFIAQSTISLR 425 Query: 434 VL 435 +L Sbjct: 426 IL 427 Lambda K H 0.319 0.137 0.394 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: 552 Number of extensions: 16 Number of successful extensions: 2 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: 436 Length of database: 427 Length adjustment: 32 Effective length of query: 404 Effective length of database: 395 Effective search space: 159580 Effective search space used: 159580 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 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