Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_078427294.1 BK574_RS02120 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_002019605.1:WP_078427294.1 Length = 520 Score = 360 bits (925), Expect = e-104 Identities = 205/514 (39%), Positives = 306/514 (59%), Gaps = 18/514 (3%) Query: 25 VRILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKMIAEE 84 V + DTTLRDGEQ+PG + K++ A +L KLG+DIIEAGF AS D AV+ +AE Sbjct: 6 VILFDTTLRDGEQTPGVNLNENDKVKIALRLEKLGIDIIEAGFAAASPGDAKAVRAVAEA 65 Query: 85 VGNCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLRKSKD 144 V + P++ ++R N+ DI +A K + FIATSPIH E KL +K Sbjct: 66 V--------HKPLVVSLARTNKNDIDEVVKAFKGITNVGIHIFIATSPIHRERKLGMTKQ 117 Query: 145 QVLETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDTVGIA 204 +V++ A V +A I+F ED+ R++ EFL +I +VI+AGAT L PDTVG Sbjct: 118 EVVDKAVESVAYASQF-FDHIEFSCEDSTRTELEFLREISEKVIEAGATVLNFPDTVGYT 176 Query: 205 MPFEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTINGIGER 264 P EY +L I +T GIE I++ HCH+DLGLA +N+I + GA Q+E INGIGER Sbjct: 177 TPEEYTELFQYILNHTRGIEKVILSCHCHDDLGLALSNSIAAMKAGALQIEGCINGIGER 236 Query: 265 AGNASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVGANAF 324 AGN + EEV + R TGIN + I KTS +V + +G+ + P+KA+VG NA+ Sbjct: 237 AGNVALEEVAALIETRSEHY--QRKTGINLKEIAKTSNLVSRLTGISIPPNKAVVGGNAY 294 Query: 325 LHESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGYKLKD 384 H SGIHQDG++K + TYEI+ PE +G + +VLGKLSGR AL+ R EELGY + D Sbjct: 295 AHSSGIHQDGVIKDKSTYEILKPESVGFSET---KLVLGKLSGRHALKKRYEELGYHVDD 351 Query: 385 TEVEGVFWQFKAVAEKKKRITDTDLRALVSNEAFNEQPIW-KLGDLQVTCGTVGFSTATV 443 +++ +F ++K + ++KK I D D+ AL+ +E NE + D+ + A V Sbjct: 352 QQLKEIFTKYKELTDRKKEIFDNDIIALLESEQPNEGTNYLSFQDVSLQVLNNKQYRAFV 411 Query: 444 KLFSIDGSMHVACSIGTGPVDSAYKAINHIVKEPAKLVKYTLGAITEGIDATATTSVEIS 503 + D + + G GP+D+ + AI+ ++ +LV Y + ++++G D+ V++S Sbjct: 412 NINGKDQQVIEGIAKGNGPIDAIFNAIDTLINLDVELVDYKITSVSQGKDSLGEVFVKVS 471 Query: 504 RGDTNHPVFSGTGGGTDVVVSSVDAYLSALNNML 537 G++ +F G G D++V+S AY+ A+N ++ Sbjct: 472 SGNS---IFQGRGMDVDIIVASTTAYIDAINRII 502 Lambda K H 0.318 0.134 0.390 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: 640 Number of extensions: 23 Number of successful extensions: 7 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: 540 Length of database: 520 Length adjustment: 35 Effective length of query: 505 Effective length of database: 485 Effective search space: 244925 Effective search space used: 244925 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: 52 (24.6 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