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_013707830.1 DESAC_RS14605 3-isopropylmalate dehydrogenase
Query= SwissProt::Q58991 (347 letters) >NCBI__GCF_000195295.1:WP_013707830.1 Length = 355 Score = 198 bits (504), Expect = 2e-55 Identities = 129/359 (35%), Positives = 196/359 (54%), Gaps = 23/359 (6%) Query: 3 KVCVIEGDGIGKEVIPEAIKILNELG-----EFEIIKGEAGLECLKKYGNALPEDTIEKA 57 K+ V+ GDG G EV+ E IK+LN + +FE I + G E K+ G LP+ +++ Sbjct: 4 KIAVLPGDGTGPEVVAEGIKVLNAIAGPAGLKFEFIHYDLGGERYKRTGEILPDSVLKEL 63 Query: 58 KEADIILFGAITSP--KPGEVKNYKSPIITLRKMFHLYANVRPINNFGIGQLIGKIADYE 115 + I GAI P KPG ++ K ++ LR Y N+RP+ + G Sbjct: 64 RGFRSIYLGAIGHPDVKPGILE--KGLLLRLRFELDQYINLRPVILYP-----GVYTPLR 116 Query: 116 FLNAKNIDIVIIRENTEDLYVG-----RERLENDTAIAERVITRKGSERIIRFAFEYAIK 170 ++I+ V++RENTE LY G + ++ A+ E + TRKG +R +++AFE K Sbjct: 117 DKGPEDINFVVVRENTEGLYAGAGGVLKYGTPDEVAVQESINTRKGVDRCLKYAFELTRK 176 Query: 171 NNR-KKVSCIHKANVLRITDGLFLEVFNEIKKHYNIEADDYL-VDSTAMNLIKHPEKFDV 228 N+ KK++ + K NVL L+ F+ + + Y A DY VD+T M ++K+PE FDV Sbjct: 177 RNKNKKLTLVGKTNVLTFAFDLWERAFHAMAQSYPDIATDYAHVDATCMWMVKNPEWFDV 236 Query: 229 IVTTNMFGDILSDEASALIGGLGLAPSANIG-DDKALFEPVHGSAPDIAGKGIANPMASI 287 +VT NMFGDI++D + + GG+G+A NI + ++FEP+ GSAP GK I NP+A+I Sbjct: 237 LVTDNMFGDIITDLGAMIQGGMGIAAGGNINPEGVSMFEPIGGSAPKYTGKNIINPLAAI 296 Query: 288 LSIAMLFDYIGEKEKGDLIREAVK-YCLINKKVTPDLGGDLKTKDVGDEILNYIRKKLK 345 + ML D++GE + I EA+K C + K T +VGD + Y LK Sbjct: 297 AAAQMLLDHLGEVKAAAAIEEAIKTVCAKHLKSLQAGKMGYSTSEVGDLVAQYAIDNLK 355 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: 377 Number of extensions: 24 Number of successful extensions: 7 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