Align 3-isopropylmalate/3-methylmalate dehydrogenase; 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; IPMDH; Beta-IPM dehydrogenase; D-malate dehydrogenase [decarboxylating]; EC 1.1.1.85; EC 1.1.1.n5; EC 1.1.1.83 (characterized)
to candidate WP_053767687.1 BVI061214_RS06265 homoisocitrate dehydrogenase
Query= SwissProt::Q58130 (333 letters) >NCBI__GCF_001280255.1:WP_053767687.1 Length = 334 Score = 309 bits (791), Expect = 7e-89 Identities = 177/336 (52%), Positives = 220/336 (65%), Gaps = 12/336 (3%) Query: 2 HKICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALDC 61 ++IC+IEGDGIG EVVPA +VLEATGLP EFV AEAG E ++R G ++PEET+E L C Sbjct: 3 YRICLIEGDGIGHEVVPAARRVLEATGLPLEFVEAEAGWETFERRGVSVPEETVEKILSC 62 Query: 62 DAVLFGAAGETAADV------IVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRENT 115 A LFGAA V I LR LD YAN+RP K+ + + RP +D +IVRENT Sbjct: 63 HATLFGAATSPTRKVPGFFGAIRYLRRRLDLYANVRPAKS-RPIPQSRPGVDLIIVRENT 121 Query: 116 EGLYKGIEAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEGKVTCAHKANVLK 175 EGLY E + + IA VI++KA ERI R A +A R + AHKANVL Sbjct: 122 EGLYVEQERRYLD-VAIADAVISKKASERIGRVALKIAEGRPCK----TLHIAHKANVLP 176 Query: 176 LTDGLFKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAAG 235 +T GLF + A ++ + +D +D M ++ +P+ FDV+VT+NL GDILSD AG Sbjct: 177 VTQGLFLDTVKEAARDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTNLLGDILSDLTAG 236 Query: 236 TVGGLGLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAADK 295 VGGLGLAPSANIGD +FEPVHGSAPDIAGK IANPTATILSA +ML YLGE E A K Sbjct: 237 LVGGLGLAPSANIGDTTAVFEPVHGSAPDIAGKGIANPTATILSAAMMLDYLGEREVARK 296 Query: 296 VEKALEEVLALGLTTPDLGGNLNTFEMAEEVAKRVR 331 VE+A++ VL G TPDLGG T + V + ++ Sbjct: 297 VERAVDLVLEKGPRTPDLGGEATTETFTQAVIEALK 332 Lambda K H 0.318 0.138 0.390 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: 302 Number of extensions: 11 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: 333 Length of database: 334 Length adjustment: 28 Effective length of query: 305 Effective length of database: 306 Effective search space: 93330 Effective search space used: 93330 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 (21.7 bits) S2: 49 (23.5 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