Align Homoserine dehydrogenase; EC 1.1.1.3 (characterized, see rationale)
to candidate 206318 DVU0890 homoserine dehydrogenase
Query= uniprot:B8DRS3_DESVM (436 letters) >lcl|MicrobesOnline__882:206318 DVU0890 homoserine dehydrogenase Length = 424 Score = 680 bits (1754), Expect = 0.0 Identities = 347/425 (81%), Positives = 379/425 (89%), Gaps = 2/425 (0%) Query: 11 KRLVIGMAGFGTVGSGLARVLDENRQWITERTGREMVIKTILVRDLAKPRAWPVPQGATL 70 K LVIGMAG GTVGSGL RVL+ENRQWI ERTGR + +K +LVRDL+KPR +P GA+L Sbjct: 2 KPLVIGMAGCGTVGSGLLRVLEENRQWIVERTGRAVQVKHVLVRDLSKPR--DLPDGASL 59 Query: 71 TADPAVLTDDPEIDVLVELMGGIAAPHAIIKRALEAGKHVVTANKALLAEDGYDLYRLAE 130 T DPAVLTDDPE+DVLVELMGGI P +I+RA+E GKHVVTANKALLAEDG+ L+RLAE Sbjct: 60 TDDPAVLTDDPEVDVLVELMGGIEKPRELIRRAIENGKHVVTANKALLAEDGFGLFRLAE 119 Query: 131 QKNVGLHHEASVAGGIPIVQTLKESLAGNRIGSLVGILNGTANYILSEMTSNGLDFATAL 190 +K VGL++EASVAGGIPIVQTLKESLAGNRI SLVGILNGTAN+ILSEMTS GLDF TAL Sbjct: 120 EKGVGLYYEASVAGGIPIVQTLKESLAGNRITSLVGILNGTANHILSEMTSAGLDFETAL 179 Query: 191 AQAQELGYAEADPTLDIEGHDTAHKLVLLIRLAYGMDYPYAELPVQGIAGIDRMDIEFAR 250 AQAQELGYAEADPTLDI+GHDTAHKLVLLIRLAYG++YPYAE+PVQGI GIDRMDIEFAR Sbjct: 180 AQAQELGYAEADPTLDIDGHDTAHKLVLLIRLAYGLEYPYAEMPVQGIRGIDRMDIEFAR 239 Query: 251 ELGFRIKLLAQVREVDGKLEAGVFPTLVKHTFLIARVGGAYNAIRLEGNAVGPVFLHGLG 310 E GFRIKLL QVREVDG+LEAGVFPTLV+HT+LIARVGGAYNAIR+EGNAVGPVFLHG G Sbjct: 240 EFGFRIKLLGQVREVDGRLEAGVFPTLVRHTYLIARVGGAYNAIRIEGNAVGPVFLHGQG 299 Query: 311 AGSLPTASAVLADLMTVARGAAPHNTGFQRQVPPRADILPPADAESSYYVRAMVPDNPGV 370 AGSLPTAS+VLADLM VAR PHNTGFQRQVPP+A ILPP DA S+YYVR MVPD+PGV Sbjct: 300 AGSLPTASSVLADLMAVARATPPHNTGFQRQVPPKASILPPDDAVSAYYVRVMVPDHPGV 359 Query: 371 LRDLAGAMADHSISIAQAIQKGQHPQGVPLVFMTHAAKASAIQGAIAQVQAAGLLLAPPV 430 LRDLAGAMADH ISIAQAIQKGQ +GVPLVFMTH A A AI AI Q++ AGLL A PV Sbjct: 360 LRDLAGAMADHGISIAQAIQKGQDKRGVPLVFMTHEAGARAISDAIEQIRQAGLLTADPV 419 Query: 431 CYRVL 435 CYRVL Sbjct: 420 CYRVL 424 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: 701 Number of extensions: 21 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: 424 Length adjustment: 32 Effective length of query: 404 Effective length of database: 392 Effective search space: 158368 Effective search space used: 158368 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 Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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