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_027722231.1 H589_RS0111950 3-isopropylmalate dehydrogenase
Query= SwissProt::Q58991 (347 letters) >NCBI__GCF_000425265.1:WP_027722231.1 Length = 355 Score = 202 bits (515), Expect = 8e-57 Identities = 133/349 (38%), Positives = 201/349 (57%), Gaps = 31/349 (8%) Query: 2 MKVCVIEGDGIGKEVIPEAIKILNELGE-----FEIIKGEAGLECLKKYGNALPEDTIEK 56 MK+C++ GDGIG E++ + IK+LN + + FE + G + + G LP+ T++ Sbjct: 1 MKICMMPGDGIGPEIMEQGIKVLNVIADRFGHNFETTEALIGGIAIDETGVPLPDATVKA 60 Query: 57 AKEADIILFGAITSPKPGEVKNYKSP---IITLRKMFHLYANVRPINNFGIGQLIGKIAD 113 KEAD +L GA+ PK + P ++ +RK L+AN+RP L ++ D Sbjct: 61 CKEADAVLLGAVGGPKWDTIDPAIRPEKGLLGIRKELSLFANLRP------AALFPQLKD 114 Query: 114 YEFLN----AKNIDIVIIRENTEDLYVGRER---LENDTAIAERVITRKGSE--RIIRFA 164 FL AK ID++++RE T +Y G R EN + + E RI + A Sbjct: 115 ACFLRPDIVAKGIDVMVVRELTGGIYFGEPRGTKEENGERMGYNTMVYYEHEVRRIAKVA 174 Query: 165 FEYAIKNNRKKVSCIHKANVLRITDGLFLEVFNEIKKHY-NIEADDYLVDSTAMNLIKHP 223 FE A + +K++ + KANVL ++ ++ E+ E+ + Y ++E VD+ AM L++ P Sbjct: 175 FE-AARKRKKRLCSVDKANVLDVSR-VWREIVIEVAEDYPDVELSHMYVDNAAMQLVRDP 232 Query: 224 EKFDVIVTTNMFGDILSDEASALIGGLGLAPSANIGD-DKALFEPVHGSAPDIAGKGIAN 282 +FDVIVT N+FGDILSDEA+ + G +G+ PSA++G+ + LFEP+HGSAPDIAG+ AN Sbjct: 233 SQFDVIVTGNLFGDILSDEAAVITGSIGMLPSASLGESNPGLFEPIHGSAPDIAGQNKAN 292 Query: 283 PMASILSIAMLFDY-IGEKEKGDLIREAVKYCLINKKVTPDL---GGDL 327 P+A+ILSIAM+ Y E+ D I AV+ L T D+ GG L Sbjct: 293 PLATILSIAMMLRYSFNMTEEADCIEAAVEKTLAQGLRTGDIMDEGGTL 341 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: 325 Number of extensions: 24 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