Align 3-isopropylmalate dehydratase large subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized)
to candidate WP_011765266.1 AZO_RS07750 aconitate hydratase AcnA
Query= curated2:Q9WYC7 (418 letters) >NCBI__GCF_000061505.1:WP_011765266.1 Length = 903 Score = 118 bits (296), Expect = 6e-31 Identities = 134/489 (27%), Positives = 205/489 (41%), Gaps = 106/489 (21%) Query: 24 VLARVDIAMAQDGTG-PLMIN--EFRELGFKEVKVPKAF-------LFIDHASPSPR--K 71 V+ARV + QD TG PL+ + R++ ++ + PK L +DH+ Sbjct: 88 VVARV---VLQDFTGVPLLCDLAAMRDVAAEQGRDPKRIEPLVPVDLVVDHSVQVDHYGS 144 Query: 72 ELSNSQKMMREFGK--------EMGVKVFDA------GDGISHQILAEKYVK----PGDL 113 ++ Q M EF + + G++ FD G GI HQI E + GDL Sbjct: 145 PIALRQNMELEFERNRERYQFLKWGMQAFDTFGVVPPGIGIVHQINLEYLFRGLREEGDL 204 Query: 114 -----VAGADSHTCTAGGLGAFGTGMGSTDVAIIFGLGQN-WFKVPETIKVVVNGKLQDG 167 + G DSHT GLG G G+G + LGQ +F P+ I V + GKL +G Sbjct: 205 YYPDTLVGTDSHTTMINGLGVVGWGVGGIEAEAAM-LGQPVYFLTPDVIGVELRGKLPEG 263 Query: 168 VYAKDIILEIARILGSDGATYKALEFHGSCIENMNVEDRLTISNMAVEVGAKAGLMPSDE 227 V A D++L + +L + K +EF G N+ V DR TI+NMA E GA G P DE Sbjct: 264 VTATDLVLTVTELLRREKVVGKFVEFFGDGTANLTVTDRATIANMAPEYGATMGFFPVDE 323 Query: 228 KTREFLKKMGREED--------FR--ELKADPDA---VYETEIEIDATTLEP-------- 266 K+ +++ GR+E FR ++ P A Y + +D T+ P Sbjct: 324 KSVAYMRGTGRDERNCALLEAWFRAQQMFGVPRAGEIDYTRTLVLDLATITPSVAGPKRP 383 Query: 267 ---------------LVSLPHYVDNVRKVSEVEKEKIKIDQ------------VFIGTCT 299 L S P + + +E +E++ + I +CT Sbjct: 384 QDRIPLGGLGARFTELFSAPTAANGFGRPAETLRERVPSGRENIALGNGDVLIAAITSCT 443 Query: 300 NGRLQDLEIALKILEKHG------KHPDVRLIVGPASRKVYMDALEK-GIIKKFVELGAA 352 N + IA +L + P ++ + P SR V D LEK G+++ ELG A Sbjct: 444 NTSNPAVLIAAGLLARKAVEAGLRVQPHIKTSLAPGSR-VVTDYLEKAGLLEPLAELGFA 502 Query: 353 VIPPGCGPCVGIHMGVLGDGERVLSTQ----------NRNFKGRMGNPNAEIYLASPATA 402 + GC C+G + + ++ NRNF+ R+ +LASP Sbjct: 503 LAGYGCTTCIGNAGDLAPEFNETIAAHHLVAAAVLSGNRNFEARIHPSIRANFLASPPLV 562 Query: 403 AATAVTGYI 411 A A+ G + Sbjct: 563 VAFALAGTV 571 Lambda K H 0.318 0.137 0.395 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: 831 Number of extensions: 39 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 418 Length of database: 903 Length adjustment: 37 Effective length of query: 381 Effective length of database: 866 Effective search space: 329946 Effective search space used: 329946 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 53 (25.0 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