Align Homoisocitrate dehydrogenase; HICDH; Homo(2)-isocitrate/homo(3)-isocitrate dehydrogenase; Isohomocitrate dehydrogenase; IHDH; NAD-dependent threo-isohomocitrate dehydrogenase; EC 1.1.1.87; EC 1.1.1.- (characterized)
to candidate WP_093393429.1 BM091_RS03260 3-isopropylmalate dehydrogenase
Query= SwissProt::Q58991 (347 letters) >NCBI__GCF_900114975.1:WP_093393429.1 Length = 355 Score = 207 bits (527), Expect = 3e-58 Identities = 132/355 (37%), Positives = 201/355 (56%), Gaps = 27/355 (7%) Query: 3 KVCVIEGDGIGKEVIPEAIKILNELGE-----FEIIKGEAGLECLKKYGNALPEDTIEKA 57 ++ I GDG G EV+ EA+K+L+ + E E ++ + G E + G LP I++ Sbjct: 7 RIAKIPGDGTGPEVVREAVKVLDAVAEKEGFKIEWVEYDLGGERYLRTGEILPAGVIDEL 66 Query: 58 KEADIILFGAITSP--KPGEVKNYKSPIITLRKMFHLYANVRPINNFGIGQLIGKIADYE 115 ++ D IL GAI P KPG ++ + ++ LR Y N+RP+ F G + Sbjct: 67 RQMDAILLGAIGHPDVKPGVLE--RGLLLELRFQLDQYVNLRPVTLFP-----GVYTPVK 119 Query: 116 FLNAKNIDIVIIRENTEDLYVG-----RERLENDTAIAERVITRKGSERIIRFAFEYAIK 170 ++ID V++RENTE LY G R+ ++ A+ E + TR G ER IRFAFEY K Sbjct: 120 DKGPEDIDFVVVRENTEGLYAGAGGILRKGTPHEVAVQESINTRMGVERCIRFAFEYCRK 179 Query: 171 NNRKK-VSCIHKANVLRITDGLFLEVFNEIKKHY-NIEADDYLVDSTAMNLIKHPEKFDV 228 N+KK V+ K NVL L+ F E+ + Y +IE D VD+ M ++K+PE FDV Sbjct: 180 RNKKKKVTLCGKTNVLIYAFDLWERTFREVAREYPDIETDYAHVDAICMWMVKNPEWFDV 239 Query: 229 IVTTNMFGDILSDEASALIGGLGLAPSANIG-DDKALFEPVHGSAPDIAGKGIANPMASI 287 IVT NMFGDI++D + + GG+G+A NI + ++FEP+ GSAP GK + NP+A+I Sbjct: 240 IVTDNMFGDIITDLGAMIQGGMGIAAGGNINPNGVSMFEPIGGSAPKYTGKNVINPLAAI 299 Query: 288 LSIAMLFDYIGEKEKGDLIREAVKYCLINKKVTPDLGG---DLKTKDVGDEILNY 339 + M+ +++GE++ + EAVK + + DLG + T++VGD + Y Sbjct: 300 CAGQMMLEHLGEEKAAQRVLEAVKRAV--ARDIKDLGAGKMGMTTQEVGDLVARY 352 Lambda K H 0.319 0.140 0.397 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: 372 Number of extensions: 19 Number of successful extensions: 6 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: 347 Length of database: 355 Length adjustment: 29 Effective length of query: 318 Effective length of database: 326 Effective search space: 103668 Effective search space used: 103668 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 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