Align Homoserine dehydrogenase; EC 1.1.1.3 (characterized, see rationale)
to candidate CCNA_01447 CCNA_01447 homoserine dehydrogenase
Query= uniprot:A0A1L6J6Q3 (430 letters) >FitnessBrowser__Caulo:CCNA_01447 Length = 429 Score = 360 bits (923), Expect = e-104 Identities = 194/422 (45%), Positives = 258/422 (61%), Gaps = 2/422 (0%) Query: 6 RVALAGLGTVGAGVIRLIDANAELIARRAGRPIEIVAVSARDRAKDRGVDITRFDWVDDM 65 RV +AGLGTVG G+++ + AG + AVSAR +++ R VDI+ W DD Sbjct: 7 RVGVAGLGTVGGGLLQFLAERPGFAP--AGDLAVVTAVSARSKSRPRTVDISNLVWFDDP 64 Query: 66 TELARHPKADVVVELIGGSDGPALALARATLAAGKGLVTANKAMIAHHGLELAQVAEKSD 125 LA P+ D+ VEL+GGSDGPA A L AGK +VTANKA+IA HG ELA +AE ++ Sbjct: 65 VALAASPEIDIFVELVGGSDGPAKAAVETALKAGKPVVTANKALIAEHGAELAALAEATN 124 Query: 126 TPMKFEAAVAGGVPVIKGLREGAAANQIDRVYGILNGTCNFILSKMEAEGRDFGEVLAEA 185 TP+ FEAAV GGVP +K +RE + I V GILNGTCNFILS+ME GR F +VL EA Sbjct: 125 TPLLFEAAVMGGVPAVKMMREALVGDDIISVAGILNGTCNFILSEMEKTGRSFADVLREA 184 Query: 186 QAAGFAEADPSFDIDGVDAAHKLSILASIAFGTQPAFGDVAIGGIRHLLAADIAEAAALG 245 Q G+AEADP+ D+ G DA HK+SILA++AFG P F I GI + DI A LG Sbjct: 185 QGLGYAEADPTMDVGGFDAGHKVSILAALAFGCAPNFAAAEIEGISEVDLLDIKLAKDLG 244 Query: 246 YRIRLLGIADLSGNGLFQRVHPHLVPLSHPLAHVLGPTNAVVAEGNFVGRLLFQGAGAGD 305 YRI+L+ A S +G+ +VHP LVPL HPLA G NA+ EG +GR+ QG GAG Sbjct: 245 YRIKLIAGAAKSEDGVAVKVHPSLVPLDHPLAQAGGALNALFIEGKRIGRIFLQGPGAGA 304 Query: 306 GPTASAVVADLIDIARTEFGPPYAMPATSLAAEPVAPTGERRGRAYLRFTVADKVGVLAE 365 GPTA+AV AD+ D+ P + PA L + G+AYLR V D+ GV+A Sbjct: 305 GPTAAAVAADIADVMTKAVRPVFQAPAGDLKPFVSIDPSKAVGKAYLRVMVQDQPGVIAA 364 Query: 366 IAAAMRDAGVSIESLIQRGAMADGSVLVAIVTHEVPERSIAQALEKLRGSPSLAGEPMWM 425 I+ + + GVSI+S +Q+ G V + +VTH PE ++ A+ ++ ++ P + Sbjct: 365 ISETLAECGVSIDSFLQKPVEGAGGVPIVLVTHATPESNLLDAISRIEKLQTVLERPRLL 424 Query: 426 HI 427 + Sbjct: 425 RV 426 Lambda K H 0.319 0.136 0.388 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: 496 Number of extensions: 18 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: 430 Length of database: 429 Length adjustment: 32 Effective length of query: 398 Effective length of database: 397 Effective search space: 158006 Effective search space used: 158006 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 (21.8 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