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_055434914.1 ASC41_RS01705 3-isopropylmalate dehydrogenase
Query= SwissProt::Q58991 (347 letters) >NCBI__GCF_001418085.1:WP_055434914.1 Length = 372 Score = 218 bits (554), Expect = 3e-61 Identities = 142/357 (39%), Positives = 202/357 (56%), Gaps = 26/357 (7%) Query: 2 MKVCVIEGDGIGKEVIPEAIKILNELG-----EFEIIKGEAGLECLKKYGNALPEDTIEK 56 + + V+ GDGIG EV +AIK+L + F + G + + N LP++T+E Sbjct: 3 LNIAVLPGDGIGPEVTKQAIKVLKAIALEFDHTFLFKEALVGAIAIDEQNNPLPDNTLEL 62 Query: 57 AKEADIILFGAITSPK----PGEVKNYKSPIITLRKMFHLYANVRPINNFGIGQLIGKIA 112 K +D ILFGAI PK P + ++ LRK LYANVRP+ + + Sbjct: 63 CKSSDAILFGAIGHPKYDNDPSAKVRPEQGLLKLRKELGLYANVRPVKAYDT------LL 116 Query: 113 DYEFLNAKNI---DIVIIRENTEDLYVGRERLENDTAIAERVI--TRKGSERIIRFAFEY 167 D L + I DI I RE T +Y G ++L D A + +R+ ERI AF+ Sbjct: 117 DKSPLKREIIEGTDISIYRELTGGIYFGEKQLSEDGNTASDLCEYSREEIERIAHLAFK- 175 Query: 168 AIKNNRKKVSCIHKANVLRITDGLFLEVFNEIKKHY-NIEADDYLVDSTAMNLIKHPEKF 226 A ++ KKV+ + KANVL T L+ V E+ Y ++ D VD+ AM +I +P++F Sbjct: 176 AAQSRSKKVTLVDKANVLE-TSRLWRRVVTELATQYPDVTLDFLFVDNAAMQMILNPKQF 234 Query: 227 DVIVTTNMFGDILSDEASALIGGLGLAPSANIGDDKALFEPVHGSAPDIAGKGIANPMAS 286 DVI+T N+FGD++SDEAS + G +GL SA++GD A+FEP+HGS P GK IANP+AS Sbjct: 235 DVILTENLFGDVISDEASVIGGSIGLLASASVGDKYAMFEPIHGSYPQATGKDIANPVAS 294 Query: 287 ILSIAMLFDYIGEKEKGDLIREAVKYCLINKKVTPDLG---GDLKTKDVGDEILNYI 340 ILS AML ++ E+ DLI+EAV+ L TPDL ++ T VGD I ++I Sbjct: 295 ILSAAMLLEHFDLHEEADLIKEAVEKSLKLNVTTPDLNTIYDNISTNKVGDFIADFI 351 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: 342 Number of extensions: 20 Number of successful extensions: 5 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: 372 Length adjustment: 29 Effective length of query: 318 Effective length of database: 343 Effective search space: 109074 Effective search space used: 109074 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