Align Probable 3-isopropylmalate dehydratase large subunit; EC 4.2.1.33; Alpha-IPM isomerase; IPMI; Isopropylmalate isomerase (uncharacterized)
to candidate GFF2253 HP15_2203 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase
Query= curated2:O27439 (419 letters) >FitnessBrowser__Marino:GFF2253 Length = 864 Score = 110 bits (275), Expect = 2e-28 Identities = 119/466 (25%), Positives = 200/466 (42%), Gaps = 76/466 (16%) Query: 4 TVSEKILARASGKDR---VEAGEIVMADIDVAMTHDLTGPLSVESFRAIGEDRVWDPEKI 60 T+++K++ +A G + V + + D TGP++ + + + + + + Sbjct: 382 TLAQKMVGKACGLEEGKGVRPNTYCEPHMTTVGSQDTTGPMTRDELKDLA-CLGFQADLV 440 Query: 61 VVIFDHQVPADSIEAAQNHMIMRDFVEEQGIRNFYDVREGVCHQVLPEKGHVVPGEVVVG 120 + F H + M DF+ +G + +G+ H L ++P V G Sbjct: 441 MQSFCHTAAYPKPVDVEMQHTMPDFIRTRGGVSLRP-GDGIIHSWLNRM--LLPDTVGTG 497 Query: 121 TDSHTCTHGALGAFATGI----GSTDMAMVFATGKLWFRVPETLRFDVRGKLREHVYAKD 176 DSHT F GI GS +A ATG + +PE++ +G+++ + +D Sbjct: 498 GDSHT-------RFPMGISFPAGSGLVAFAAATGVMPLDMPESVLVRFKGEMQPGITLRD 550 Query: 177 VILNI---------------------IGRV-GADGATYMACEFAGE-------------- 200 ++ I GR+ +G ++ E A E Sbjct: 551 LVHAIPLYGIKQGMLTVEKKGKINEFSGRILEIEGLEHLTVEQAFELSDASAERSAAGCT 610 Query: 201 ------TVAEMSVSDRMVLSNMAIEMGGKTGIVEPDEKTLNYVRRRSGKPW----RVFKT 250 +VAE S+ +L M E G D +TL R + + W ++ + Sbjct: 611 INLSEDSVAEYLRSNITMLRWMIAEGYG-------DPRTLER-RAQQMEEWLADPKLMRA 662 Query: 251 DPDAPSLSVMEVDVSDL-EPQVACPHNVDNVKPVTEVEGTEIDQVFLGSCTNGRLSDLRD 309 D DA V+E+D++D+ EP V CP++ D+ K ++EV G ++D+VF+GSC + R Sbjct: 663 DKDAEYAHVIEIDLADIKEPIVCCPNDPDDAKFLSEVAGDKVDEVFIGSCMT-NIGHFRA 721 Query: 310 AAAILKNRKVSDSVRMLVIPASREVYRRALDEGLIEIFVDAGALVCNPCCGPCLGGHVGL 369 A +L+ K S R+ + P ++ + ++EG + AG P C C+G Sbjct: 722 AGKLLEQHKGPLSTRLWMSPPTKMDQAQLMEEGYFNTYGTAGVRTEMPGCSLCMGNQ-AR 780 Query: 370 VGPGEVSLSTSNRNFRGRQGSPEAEVYLSSAAVAAASAVKGSITHP 415 V P LSTS RNF R G A VYL+SA +AA AV G + P Sbjct: 781 VAPKSTVLSTSTRNFPNRLGD-GANVYLTSAELAAVGAVLGKLPSP 825 Lambda K H 0.318 0.135 0.396 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: 821 Number of extensions: 55 Number of successful extensions: 5 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: 419 Length of database: 864 Length adjustment: 37 Effective length of query: 382 Effective length of database: 827 Effective search space: 315914 Effective search space used: 315914 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: 53 (25.0 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 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