Align homoserine dehydrogenase (EC 1.1.1.3) (characterized)
to candidate WP_012409281.1 NPUN_RS13890 homoserine dehydrogenase
Query= BRENDA::P19582 (433 letters) >NCBI__GCF_000020025.1:WP_012409281.1 Length = 428 Score = 346 bits (888), Expect = e-100 Identities = 184/429 (42%), Positives = 283/429 (65%), Gaps = 9/429 (2%) Query: 4 IRVGLLGLGTVGSGVVKIIQDHQDKLMHQVGCPVTIKKVLVKDLEKKREVDLPKEVLTTE 63 +++G+LGLGTVG+G V+++QD + H + + I +V VK L+K R V+L EV+TT+ Sbjct: 3 VKLGILGLGTVGTGTVQLLQDKAGR--HPLLQEIEIYRVGVKSLDKPRAVELSTEVVTTD 60 Query: 64 VYDVIDDPDVDVVIEVIGGVEQTKQYLVDALRSKKHVVTANKDLMAVYGSELLAEAKENG 123 + +++DP VD+V+EV+GG+E + ++ AL + KHVVTANK +A +G+E+ A + G Sbjct: 61 LESIVNDPAVDIVVEVMGGLEPARSLILKALSNGKHVVTANKAAIARFGAEIFTTANQAG 120 Query: 124 CDIYFEASVAGGIPILRTLEEGLSSDRITKMMGIVNGTTNFILTKMIKEKSPYEEVLKEA 183 + EA+V GGIP+++ L++ LS +RI + GIVNGTTN+ILT+M E S + +VL +A Sbjct: 121 VYVMLEAAVGGGIPVIQPLKQSLSVNRIHTVTGIVNGTTNYILTRMQTEGSNFSDVLADA 180 Query: 184 QDLGFAEADPTSDVEGLDAARKMAILARLGFSMNVDLEDVKVKGISQITDEDISFSKRLG 243 Q LG+AEADPT+DV+GLDAA K+AILA LGF ++L+DV +GI Q++ DI+++++LG Sbjct: 181 QRLGYAEADPTADVDGLDAADKIAILASLGFGGRINLQDVYTEGIRQVSKTDIAYAEKLG 240 Query: 244 YTMKLIGIAQRD--GSKIEVSVQPTLLPDHHPLSAVHNEFNAVYVYGEAVGETMFYGPGA 301 + +KL+ IA+RD S + V V PTL+P HPL++++ +NA+ V GE +G+ MF+GPGA Sbjct: 241 FVIKLLAIAKRDTPSSPLSVRVHPTLVPQAHPLASINGVYNAILVEGEPIGQVMFFGPGA 300 Query: 302 GSMPTATSVVSD---LVAVMKNMRLGVTGNSFVGPQYEKNMKSPSDIYAQQFLRIHVKDE 358 G+ TA++V SD LVAV+K G Q + +++ + + R D+ Sbjct: 301 GAGATASAVTSDILNLVAVLKTNTAVANPLIACGHQEYCQIAPMAELITRFYARFLTNDQ 360 Query: 359 VGSFSKITSVFSERGVSFEKILQLPIKGHDELAEIVIVTHHTSEADFSDILQNLNDLEVV 418 G K+ + F GVS E I+Q +G ELAEIV+VTH E +F L + +LE + Sbjct: 361 PGVIGKLGTCFGNYGVSLESIVQTGFQG--ELAEIVVVTHDVPEGNFRQALAEIQNLEAI 418 Query: 419 QEVKSTYRV 427 + + S RV Sbjct: 419 ESIPSLLRV 427 Lambda K H 0.316 0.135 0.372 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: 419 Number of extensions: 18 Number of successful extensions: 3 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: 433 Length of database: 428 Length adjustment: 32 Effective length of query: 401 Effective length of database: 396 Effective search space: 158796 Effective search space used: 158796 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 (21.6 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