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_010875823.1 MTH_RS00845 homoisocitrate dehydrogenase
Query= SwissProt::Q58130 (333 letters) >NCBI__GCF_000008645.1:WP_010875823.1 Length = 331 Score = 356 bits (914), Expect = e-103 Identities = 189/336 (56%), Positives = 239/336 (71%), Gaps = 15/336 (4%) Query: 1 MHKICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALD 60 M++I VI GDGIG EV+ A + VL+A + FEF +AEAG+E ++R G LPEET++ Sbjct: 1 MYRITVIPGDGIGVEVMEAALHVLQALEIEFEFTHAEAGNECFRRCGDTLPEETLKLVRK 60 Query: 61 CDAVLFGAA----GETAADVIVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRENTE 116 DA LFGA G+ +A I+ LR LD +AN+RPVK+ GV CL PD+D+VIVRENTE Sbjct: 61 ADATLFGAVTTVPGQKSA--IITLRRELDLFANLRPVKSLPGVPCLYPDLDFVIVRENTE 118 Query: 117 GLYKGIEAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEG--KVTCAHKANVL 174 LY G E EG +A R+IT A RI +FAF A+ KEG KVT HKANVL Sbjct: 119 DLYVGDEEYTPEG-AVAKRIITRTASRRISQFAFQYAQ------KEGMQKVTAVHKANVL 171 Query: 175 KLTDGLFKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAA 234 K TDG+F+ FYKVA EY ++A DYY+DA MY+IT+PQ F +VT+NLFGDILSD AA Sbjct: 172 KKTDGIFRDEFYKVASEYPQMEANDYYVDATAMYLITQPQEFQTIVTTNLFGDILSDEAA 231 Query: 235 GTVGGLGLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAAD 294 G +GGLGLAPSANIG+++ LFEPVHGSAP IAGK IANPTA IL+ LML++L + + A Sbjct: 232 GLIGGLGLAPSANIGEKNALFEPVHGSAPQIAGKNIANPTAMILTTTLMLKHLNKKQEAQ 291 Query: 295 KVEKALEEVLALGLTTPDLGGNLNTFEMAEEVAKRV 330 K+EKAL++ L G+ TPDLGG +T EMAE + + + Sbjct: 292 KIEKALQKTLMRGIMTPDLGGTASTMEMAEAIKEEI 327 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: 321 Number of extensions: 17 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: 331 Length adjustment: 28 Effective length of query: 305 Effective length of database: 303 Effective search space: 92415 Effective search space used: 92415 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