Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (characterized)
to candidate WP_158211654.1 BK574_RS13545 homoserine dehydrogenase
Query= SwissProt::P52985 (428 letters) >NCBI__GCF_002019605.1:WP_158211654.1 Length = 410 Score = 235 bits (599), Expect = 2e-66 Identities = 148/426 (34%), Positives = 245/426 (57%), Gaps = 27/426 (6%) Query: 3 VNIAILGFGTVGTGLPTLLSENKEKLAKILDEEIVISKVLMRDNKAIEKARSQGFNYDFV 62 ++I I+G+GTVG+G+ L+ +KE+L L +EI + KVL+RD K ++ +QG Sbjct: 2 LSIGIIGYGTVGSGVYERLTSSKEELQSALKKEIQVKKVLVRDCK--KERNNQGAKQ--C 57 Query: 63 LNLDDI-LADSEISIVVELMGRIEPAKTYITQAIEAGKNVVTANKDLLAVHGVELRSLAQ 121 + D + ++ +V E +G +EPA+ YI + I+AG +++TANK+L+A HG EL LA+ Sbjct: 58 MTSDPVNFFQNQYDVVFEAIGGVEPARDYIIKLIQAGTSIITANKELIAKHGAELEKLAK 117 Query: 122 KHHVALYYEAAVAGGIPILRTLANSFSSDKITHLLGILNGTSNFMMTKMSEEGWTYDESL 181 ++ V L +EAAV GGIPI+ + F++ I + GILNGT+N+++T+M E+ +D+ L Sbjct: 118 EYQVYLGFEAAVGGGIPIVNSFKTLFTTTPIRSVSGILNGTTNYILTEMKEKNRQFDDVL 177 Query: 182 AKAQELGYAESDPTNDVDGIDASYKLAILSEFAFGMTLAPDDIAKSGLRSIQKTDVEIAQ 241 A+A+ LGYAE+DPT+D++G DA YK+ ILS AF ++ + G+ ++ +E A+ Sbjct: 178 AEAKVLGYAEADPTDDIEGYDALYKIRILSRLAFNEWPREENFSCKGISGMEVEAIEFAE 237 Query: 242 QFGYVLKLTGEINEVDSGIFAEVSPTFLPKSHPLASVNGVMNAVFIESEGIGDSVFYGAG 301 + G +KL + D I VSP+F+ ++HPL ++NGV N V I+ E + G G Sbjct: 238 RQGLTIKLIAKTANEDGVISGFVSPSFVTQTHPLYNINGVTNGVCIDGETVDCITMSGPG 297 Query: 302 AGQKPTATSVLADIVRIVKRVKDGTIGKSFNEY-ARSTSLANPHDIENKYYFSVETPDST 360 AG++ TA S++ D V + + F + R L+N + NK V D Sbjct: 298 AGKEATANSMVEDFV----------LHEQFQGFERRKVRLSN--QVSNKETKVVVFVDEF 345 Query: 361 GQLLLLVELFT-SENVSFEQVLQQKGNGKRAVVVIISHKINRVQLSAIQDKLNQEKDFKL 419 + ++++L T S+ + E + NGK A++V + + L + L Q+ + L Sbjct: 346 EKEEVVLQLRTISDCIDTEDTM----NGKLALIVKLGYGKTVYDL----ETLIQKSSYPL 397 Query: 420 LNRFKV 425 L F V Sbjct: 398 LGDFSV 403 Lambda K H 0.315 0.133 0.363 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: 411 Number of extensions: 23 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: 428 Length of database: 410 Length adjustment: 32 Effective length of query: 396 Effective length of database: 378 Effective search space: 149688 Effective search space used: 149688 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: 50 (23.9 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