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_066328409.1 BLR17_RS00965 3-isopropylmalate dehydrogenase
Query= SwissProt::Q58991 (347 letters) >NCBI__GCF_900100165.1:WP_066328409.1 Length = 351 Score = 208 bits (530), Expect = 1e-58 Identities = 134/348 (38%), Positives = 197/348 (56%), Gaps = 20/348 (5%) Query: 2 MKVCVIEGDGIGKEVIPEAIKILNELGE---FEIIKGEA--GLECLKKYGNALPEDTIEK 56 + + ++ GDGIG EVI +A+K+ + + + EI A G + G P+ T E Sbjct: 3 LNIALLAGDGIGPEVIDQAVKVSDAIAQKFGHEITWKPALTGAAAIDAVGEPYPDSTHEV 62 Query: 57 AKEADIILFGAITSPK----PGEVKNYKSPIITLRKMFHLYANVRPINNFGIGQLIGKIA 112 K AD +LFGAI PK P + ++ +RK L+ANVRP F L+ K + Sbjct: 63 CKNADAVLFGAIGHPKYDNDPSAPVRPEQGLLKMRKALGLFANVRP--TFTFPSLLDK-S 119 Query: 113 DYEFLNAKNIDIVIIRENTEDLYVGRERLEN--DTAIAERVITRKGSERIIRFAFEYAIK 170 + + D+V +RE T +Y G + ++ DTA V TR+ +R+ + FE A+ Sbjct: 120 PLKRERIEGTDLVFLRELTGGIYFGEKGRKDGGDTAFDNCVYTREEVQRLAKKGFELAMT 179 Query: 171 NNRKKVSCIHKANVLRITDGLFLEVFNEIKKHY-NIEADDYLVDSTAMNLIKHPEKFDVI 229 + KK+ C+ KANVL T L+ E ++K Y +E VD+ AM L++ P +DV+ Sbjct: 180 RS-KKLCCVDKANVLE-TSRLWRETVQAMEKDYPEVEVSYEFVDAVAMRLVQWPNSYDVL 237 Query: 230 VTTNMFGDILSDEASALIGGLGLAPSANIGDDKALFEPVHGSAPDIAGKGIANPMASILS 289 +T N+FGDIL+DEAS + G +GL PSA++G + +LFEP+HGS P G IANPMA++LS Sbjct: 238 ITENLFGDILTDEASVISGSMGLMPSASMGAEVSLFEPIHGSYPQATGLNIANPMATVLS 297 Query: 290 IAMLFDYIGEKEKGDLIREAVKYCLINKKVTPDLGGDLK---TKDVGD 334 AM+F+ G E+G +R+AV L VT DL K TK+VGD Sbjct: 298 AAMMFENFGLMEEGKAMRDAVNKALEAGVVTEDLANGGKAYGTKEVGD 345 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: 318 Number of extensions: 17 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: 351 Length adjustment: 29 Effective length of query: 318 Effective length of database: 322 Effective search space: 102396 Effective search space used: 102396 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 26 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