Align homoserine dehydrogenase (EC 1.1.1.3) (characterized)
to candidate WP_005816736.1 DHAF_RS12295 homoserine dehydrogenase
Query= BRENDA::D8WXQ1 (432 letters) >NCBI__GCF_000021925.1:WP_005816736.1 Length = 431 Score = 405 bits (1042), Expect = e-117 Identities = 211/427 (49%), Positives = 298/427 (69%), Gaps = 2/427 (0%) Query: 1 MEAIQVGLLGLGTVGSGVVKIIENHQDKLMHQVGCPVKVKKILVQDLNKKRDVDVDPAQL 60 M+ +++GLLGLGTVGSGV++I+E + + + ++ +KV K+LV++L R + D L Sbjct: 1 MQVVKIGLLGLGTVGSGVIQILEQNANDIQNRSLSQIKVSKVLVRNLKAPRSIAGD-FTL 59 Query: 61 TTNADDILQDPDIDVVIEVMGGIEETRNYLLKALSEKKHVVTANKDLMAVYGSELLTAAS 120 T A D+L DPDI +V+EVMGGIE + Y+L+A + K+VVTANKDL+A++G ELL AA Sbjct: 60 TDQAADVLTDPDISIVVEVMGGIEPAKTYILEAFKQGKNVVTANKDLLALHGQELLDAAK 119 Query: 121 ANGCDLFYEASVAGGIPILRSLVDGLASDRITKMMGIVNGTTNYILTKMSKHGRAYEEVL 180 G DL++EASVAGGIPI+ +L LA +RI++++GI+NGTTNYILT M++ GR Y+EVL Sbjct: 120 EAGKDLYFEASVAGGIPIIAALKQSLAGNRISEVLGIINGTTNYILTAMTEQGRDYQEVL 179 Query: 181 KEAQELGYAEADPASDVEGLDAARKMAILATLGFSMKIDLDDVKVEGITRITEEDIQYGK 240 KEAQELGYAEADP +DV+GLDAARK+AILA++ F+ ++ ++DV VEGI +IT EDI Y + Sbjct: 180 KEAQELGYAEADPTADVDGLDAARKLAILASIAFNSRVTVNDVYVEGIAKITSEDIAYAR 239 Query: 241 QLGYTMKLIGIAHREGEKVEVSVQPTLLSDSHPLASVNDEYNAVYVYGEAVGETMFYGPG 300 +L T+KL+ +A + + +EV V P + D+HPLA+V+ +NA+YV G+AVGETMFYG G Sbjct: 240 ELNSTIKLLAVAKAQADGIEVRVHPAFVPDNHPLAAVSGVFNAIYVVGDAVGETMFYGRG 299 Query: 301 AGSLPTATAVVSDLVGVMKNMRLGVNGANAVTPQYQKKLKGPDEIYSKFFLRLHVKDEVG 360 AGSLPT +AVVSD++ V++N+ T + +K + S F++RL VKDE Sbjct: 300 AGSLPTGSAVVSDIIQVVRNINADSTANINCTCYNELAIKSEQDFKSAFYIRLRVKDEPR 359 Query: 361 VFANITSIFSEHSVSFEKILQMPLKENGLAEIVLVTHQASLQDYEDILVKLRDLNAVHEI 420 V A + +F+E VSF I+Q K+ AEIVLVTH + L +R + V I Sbjct: 360 VLATLALLFAEAGVSFASIIQKQ-KKRQEAEIVLVTHPTQESCLREALDSVRAYSKVLSI 418 Query: 421 KSSYRVE 427 + R E Sbjct: 419 HNVIRFE 425 Lambda K H 0.316 0.134 0.368 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: 462 Number of extensions: 15 Number of successful extensions: 4 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: 432 Length of database: 431 Length adjustment: 32 Effective length of query: 400 Effective length of database: 399 Effective search space: 159600 Effective search space used: 159600 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