Align 3-isopropylmalate dehydratase large subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized)
to candidate PfGW456L13_4052 Aconitate hydratase (EC 4.2.1.3)
Query= curated2:Q9WYC7 (418 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4052 Length = 913 Score = 101 bits (252), Expect = 8e-26 Identities = 123/491 (25%), Positives = 199/491 (40%), Gaps = 111/491 (22%) Query: 25 LARVDIAMAQDGTGPLMINEFRELGFKEVKVPKAFLFIDHASPSPRKELSNSQKMMREFG 84 LA + AMA+ G P IN + V + +D + S E + +M R Sbjct: 100 LAAMRAAMAKAGGNPQRINPLSPVDL----VIDHSVMVDKFASSSAFEQNVDIEMQRNGE 155 Query: 85 K----EMGVKVFD------AGDGISHQILAE--------------KYVKPGDLVAGADSH 120 + G FD G GI HQ+ E Y P LV G DSH Sbjct: 156 RYAFLRWGQSAFDNFSVVPPGTGICHQVNLEYLGRTVWTKDEDGRTYAFPDTLV-GTDSH 214 Query: 121 TCTAGGLGAFGTGMGSTDVAIIFGLGQNW-FKVPETIKVVVNGKLQDGVYAKDIILEIAR 179 T GLG G G+G + LGQ +PE I + GKL++G+ A D++L + + Sbjct: 215 TTMINGLGVLGWGVGGIEAEAAM-LGQPVSMLIPEVIGFKLTGKLKEGITATDLVLTVTQ 273 Query: 180 ILGSDGATYKALEFHGSCIENMNVEDRLTISNMAVEVGAKAGLMPSDEKTREFLKKMGRE 239 +L G K +EF+G + ++ + DR TI+NMA E GA G P D+ T ++L+ GR Sbjct: 274 MLRKKGVVGKFVEFYGDGLADLPLADRATIANMAPEYGATCGFFPVDDITLDYLRLSGRP 333 Query: 240 EDFREL-----KAD-------PDAVYETEIEIDATTLEPL----------VSLPHYVDNV 277 + +L KA + V+ + +D ++E V+LP+ Sbjct: 334 LETVQLVEAYSKAQGLWRLPGQEPVFTDSLALDMGSVEACLAGPKRPQDRVTLPNVAQAF 393 Query: 278 RKVSEVE-----KEKIKIDQ-----VFIG------------------------------T 297 ++++ KE+ +++ V +G + Sbjct: 394 SDFTDLQFKPTSKEEGRLESEGGGGVAVGNADMAGEADYDYEGQTYRLKNGAVVIAAITS 453 Query: 298 CTNGRLQDLEIALKILEKHG------KHPDVRLIVGPASRKVYMDALEKGIIKKFVELGA 351 CTN + +A ++ K + P V+ + P S+ V G+ + ELG Sbjct: 454 CTNTSNPSVMMAAGLVAKKAVEKGLKRKPWVKSSLAPGSKVVTDYYKAAGLTQYLDELGF 513 Query: 352 AVIPPGCGPCVGIHMGVLGDG-ERVLS----------TQNRNFKGRMGNPNAEIYLASPA 400 A++ GC C+G + G L + E+ + + NRNF+GR+ +LASP Sbjct: 514 ALVGYGCTTCIG-NSGPLSEPIEKAIQQADLTVASVLSGNRNFEGRVHPLVKTNWLASPP 572 Query: 401 TAAATAVTGYI 411 A A+ G + Sbjct: 573 LVVAYALAGTV 583 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: 769 Number of extensions: 43 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 418 Length of database: 913 Length adjustment: 37 Effective length of query: 381 Effective length of database: 876 Effective search space: 333756 Effective search space used: 333756 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