Align Homoserine dehydrogenase; EC 1.1.1.3 (characterized, see rationale)
to candidate SMc00293 SMc00293 homoserine dehydrogenase
Query= uniprot:A0A1L6J6Q3 (430 letters) >lcl|FitnessBrowser__Smeli:SMc00293 SMc00293 homoserine dehydrogenase Length = 440 Score = 375 bits (962), Expect = e-108 Identities = 203/434 (46%), Positives = 275/434 (63%), Gaps = 7/434 (1%) Query: 1 MTEPLRVALAGLGTVGAGVIRLIDANAELIARRAGRPIEIVAVSARDRAKDRGVDITRFD 60 M + L++ +AGLGTVGA ++R++ E +A GR IEI AV+ARDR+KDRGV +T Sbjct: 1 MADALKIGIAGLGTVGASLVRILQDRHETMATTCGRAIEITAVAARDRSKDRGVKLTGIA 60 Query: 61 WVDDMTELARHPKADVVVELIGGSDGPALALARATLAAGKGLVTANKAMIAHHGLELAQV 120 W +D LA DV VEL+GG+ PA + +A L G +VTANKA++A HG+ELA++ Sbjct: 61 WFEDAVSLASEADVDVFVELMGGAGDPAYSCVKAALTRGVHVVTANKALLAAHGIELAEI 120 Query: 121 AEKSDTPMKFEAAVAGGVPVIKGLREGAAANQIDRVYGILNGTCNFILSKMEAEGRDFGE 180 AE+ + +EAAVAGG+PVIK LRE N I RVYGI+NGTCN+IL+KME EG F E Sbjct: 121 AEQHGALLNYEAAVAGGIPVIKALRESMTGNTISRVYGIMNGTCNYILTKMEKEGLSFEE 180 Query: 181 VLAEAQAAGFAEADPSFDIDGVDAAHKLSILASIAFGTQPAFGDVAIGGIRHLLAADIAE 240 L EAQ G+AEADP+FDI+G D AHKLSIL S+AFGT A D+ + GI ++ DI Sbjct: 181 CLKEAQRLGYAEADPAFDIEGNDTAHKLSILTSLAFGTAIAADDIYLEGITNISIEDIQA 240 Query: 241 AAALGYRIRLLGIADLSGNGLFQRVHPHLVPLSHPLAHVLGPTNAVVAEGNFVGRLLFQG 300 A+ LGYRI+LLG+A + +G+ QRVHP +VP +A V G TNAV E + +G LL G Sbjct: 241 ASDLGYRIKLLGVAQRTDSGIEQRVHPTMVPHDTVIAQVDGVTNAVAIESDILGELLMVG 300 Query: 301 AGAGDGPTASAVVADLIDIARTEFG----PPYAMPATSLAAEPVAPTGERRGRAYLRFTV 356 GAG TASAV+ D+ DIA++ G P + PA +L A G ++R V Sbjct: 301 PGAGGDATASAVLGDIADIAKSRPGAQHVPAFGRPAKALLPYKRARMQSHEGGYFIRLKV 360 Query: 357 ADKVGVLAEIAAAMRDAGVSIESLIQRGA-MADGS--VLVAIVTHEVPERSIAQALEKLR 413 D+ GV A +A M + +S+ES++Q AD + + +VTH E S+ +A+ ++ Sbjct: 361 VDRTGVFANVAKHMAENDISLESIMQHSKHYADPAEPKTIILVTHATSEASVRKAIVSIK 420 Query: 414 GSPSLAGEPMWMHI 427 G L GEP + I Sbjct: 421 GEGYLVGEPQVIRI 434 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: 466 Number of extensions: 11 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: 440 Length adjustment: 32 Effective length of query: 398 Effective length of database: 408 Effective search space: 162384 Effective search space used: 162384 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