Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate GFF785 HP15_764 homoserine dehydrogenase
Query= BRENDA::Q9WZ17 (739 letters) >FitnessBrowser__Marino:GFF785 Length = 433 Score = 202 bits (514), Expect = 3e-56 Identities = 145/408 (35%), Positives = 218/408 (53%), Gaps = 16/408 (3%) Query: 17 VRKVRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLG-VPKEE 75 ++ V VGI GLGTVGG + +L I R G I++V +R ++ LG VP Sbjct: 1 MKDVSVGICGLGTVGGGTFNVLTRNARLIAGRAGCNIRITRVASRRAREDMDLGDVP--- 57 Query: 76 IAFDFDDLILNSDV--VVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYI 133 + D D++ + DV VVE IGG D A +LV A+ G+ VVT NK LI+ +GNE E Sbjct: 58 FSTDIYDVVNDPDVDIVVELIGGYDAAKELVLAAIRNGKHVVTANKALIAVHGNEIFEAA 117 Query: 134 KKRKLF--FEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMSKGRHFEEVL 191 +K + +EA V GGIP+I +++ + ++ I GI+NGT NYILTEM GR F EVL Sbjct: 118 EKAGVVVAYEAGVAGGIPVIKAVREGMAANRIDWIAGIINGTGNYILTEMRAGREFSEVL 177 Query: 192 KEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEIV 251 KEAQ+LGYAEADPT D+EG D A+K+++LA G EGI++I P + Sbjct: 178 KEAQDLGYAEADPTFDVEGIDAAHKLTILASAGFGVPLQFEKGFTEGISKITPYDIAHAE 237 Query: 252 RSGKKLKLIGELDFSTNRYEVRLR-EVTPEDPFF-NVDGVDNAIEVSTDLAGDFLLKGRG 309 G ++K +G + E+R+ + P+ VDGV NA+ V D G + G G Sbjct: 238 LLGYRIKHLGIARRRDDGIELRVHPTLVPQSHLIAQVDGVLNAVLVDGDAVGQTMYYGPG 297 Query: 310 AGGYPTASAVIADLFRVAKYKVLGGAEKFSVVVMKFGGAAISDVE--KLEKVAEKIIKRK 367 AG T SAVIAD+ VA + + K V + F A+ D++ +E + R Sbjct: 298 AGDEATGSAVIADIVDVA--RAVATESKLRVPYLGFSPDAMEDLDVLSMEDIQSAYYLRI 355 Query: 368 KSGVKPVVVLSAMGDTTDHLIELAKTIDENPDPRE--LDLLLSTGEIQ 413 + +P V+ ++H I + + + + ++ + +++ T +Q Sbjct: 356 TALDRPGVLAKIASILSEHGINIESIMQKESELKDGRIPVIILTHTVQ 403 Score = 31.2 bits (69), Expect = 1e-04 Identities = 13/25 (52%), Positives = 19/25 (76%) Query: 607 DKPGVAARIMRTLSQMGVNIDMIIQ 631 D+PGV A+I LS+ G+NI+ I+Q Sbjct: 359 DRPGVLAKIASILSEHGINIESIMQ 383 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: 784 Number of extensions: 41 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: 433 Length adjustment: 36 Effective length of query: 703 Effective length of database: 397 Effective search space: 279091 Effective search space used: 279091 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