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_029767971.1 HALAL_RS0113465 3-isopropylmalate dehydrogenase
Query= SwissProt::Q58991 (347 letters) >NCBI__GCF_000527155.1:WP_029767971.1 Length = 344 Score = 209 bits (533), Expect = 6e-59 Identities = 127/357 (35%), Positives = 210/357 (58%), Gaps = 26/357 (7%) Query: 1 MMKVCVIEGDGIGKEVIPEAIKILN-ELGEFEIIKGEAGLECLKKYGNALPEDTIEKAKE 59 M + VI GDGIGKEVI +A+K++ L ++E ++ + G G LP+ + + Sbjct: 1 MSSIAVIPGDGIGKEVIDQAMKVVRLVLPDWEAVEYDLGASRYHATGEVLPDSVLSELDT 60 Query: 60 ADIILFGAITSPK--PGEVKNYKSPIITLRKMFHLYANVRPINNF-GIGQLIGKIADYEF 116 D IL GA+ P PG ++ + ++ LR F Y N+RP + G+ + K+ E Sbjct: 61 HDAILLGAVGDPSVPPGVLE--RGLLLRLRFEFDQYVNLRPSRLYPGVASPLAKVQPGE- 117 Query: 117 LNAKNIDIVIIRENTEDLYVGRE-RLENDTAIA----ERVITRKGSERIIRFAFEYAIKN 171 +D +++RE TE LY G L TA E + TR G ER++R AFE A ++ Sbjct: 118 -----VDFIVVREGTEGLYAGAGGNLHTGTAAEIATEESLNTRYGVERVVRDAFERA-RS 171 Query: 172 NRKKVSCIHKANVLRITDGLFLEVFNEIKKHYNIEADDYL-VDSTAMNLIKHPEKFDVIV 230 R +++ +HK NVL GL+ F ++ + Y DY VD+ AM ++ P+ +DV+V Sbjct: 172 RRGRLTLVHKTNVLSHAGGLWNRAFADVAEEYRDVVTDYQHVDAAAMFMVNRPQDYDVVV 231 Query: 231 TTNMFGDILSDEASALIGGLGLAPSANIGDDK---ALFEPVHGSAPDIAGKGIANPMASI 287 T N+FGDI++D A+A+ GG+GLA S + D+ ++FEPVHGSAPDIAG+GIA+P+A+I Sbjct: 232 TDNLFGDIITDIAAAVTGGIGLAASGCVNPDRTHPSMFEPVHGSAPDIAGQGIADPIAAI 291 Query: 288 LSIAMLFDYIGEKEKGDLIREAVKYCLINKKVTPDLGGDLKTKDVGDEILNYIRKKL 344 +S ++L +++GE + +++E+++ L ++ +G T+ VGD + + + ++L Sbjct: 292 MSASLLLEHVGEAKAATVVQESIERELSSRSPGQAVG----TEAVGDRVASDVEQRL 344 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: 315 Number of extensions: 26 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: 344 Length adjustment: 29 Effective length of query: 318 Effective length of database: 315 Effective search space: 100170 Effective search space used: 100170 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