Align 3-isopropylmalate dehydratase large subunit 2; EC 4.2.1.33; Alpha-IPM isomerase 2; IPMI 2; Isopropylmalate isomerase 2 (uncharacterized)
to candidate WP_029908844.1 P166_RS0103590 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase
Query= curated2:Q1AVC5 (424 letters) >NCBI__GCF_000711315.1:WP_029908844.1 Length = 857 Score = 107 bits (267), Expect = 1e-27 Identities = 122/451 (27%), Positives = 188/451 (41%), Gaps = 54/451 (11%) Query: 3 HTLAEKLLISHSEVDDASPGDIIMVRCDLVMANDVSGPVAFRQMERMGVQRVFDPSKVVM 62 ++LA+K++ ++ PG V + D +G + +M+ + F V+ Sbjct: 372 YSLAQKMVGKACGIEGVRPGMYCEPHMTTVGSQDTTGAMTRDEMKELACLG-FSADLVMQ 430 Query: 63 VSDHFMPAKDARSAALQKRLKSWSDLQGVYYYGQGRGGIEHTVLVEDGWIVPGMVIAGGD 122 H LQ L + +G G G I H+ L + ++P V GGD Sbjct: 431 SFCHTAAYPKPVDIKLQHSLPDFMTSRGGVALRPGDGVI-HSWL--NRLLLPDTVGTGGD 487 Query: 123 SHTCTYGALGAFGTGLGSTDIAACLAFGEFWQQVPGTIQVEFTGHKGSFVAGKDLILAV- 181 SHT + +F G G A L G +P ++ V F G + +DL+ A+ Sbjct: 488 SHT-RFPIGISFPAGSGLVAFGATL--GVMPLNMPESVLVRFKGEMQPGITLRDLVNAIP 544 Query: 182 -------IADIGVGGGANA----VLEFVGEGAASLSLDDRLAVANMAVEAGAETGIFPAD 230 + + G N VLE EG L ++ +++ + E A + Sbjct: 545 YQAIQDGLLTVEKKGKKNIFNGRVLEI--EGLDHLKVEQAFELSDASAERSANGCVVKLA 602 Query: 231 EVT----------------------ARYLDRRAD--REW--HPE--RSDPDASYVRKVKI 262 E AR L RR D + W PE +D DA Y ++I Sbjct: 603 EEPIIEYLKSNMALIDWMVENGYQDARTLLRRRDEMQAWIDAPELLEADADADYAAVIEI 662 Query: 263 DLNSL-EPLVALPHSPGNVVAVSEARGTKIDQVYIGNCSNGTITDLRQTAEILRGNRVHP 321 DLN++ EP+VA P+ P +V +S G KID+V+IG+C I R ++L N + Sbjct: 663 DLNTIKEPIVACPNDPDDVKLLSAVSGDKIDEVFIGSCMT-NIGHYRAAGKVLE-NMKNV 720 Query: 322 DVRAIIVPASQKVYRQAISEGLIDVFVEAGAVVSTPTCGACFGGHMGVLAEGERAITTTN 381 R I P ++ RQ I EG ++ + GA P C C G V A+G +T+ Sbjct: 721 PTRLWIAPPTKMDERQLIEEGYYSIYGKVGARTEMPGCSLCMGNQARV-ADGATVFSTST 779 Query: 382 RNFKGRMGSPLAEVCLANAYVAAAAAVAGEI 412 RNF R+G+ A V L +A +AA A G I Sbjct: 780 RNFPNRLGNG-ANVYLGSAELAAVCAAVGRI 809 Lambda K H 0.319 0.135 0.401 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: 686 Number of extensions: 33 Number of successful extensions: 5 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: 424 Length of database: 857 Length adjustment: 37 Effective length of query: 387 Effective length of database: 820 Effective search space: 317340 Effective search space used: 317340 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 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