Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_013840144.1 DESRU_RS00330 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_000215085.1:WP_013840144.1 Length = 501 Score = 405 bits (1040), Expect = e-117 Identities = 229/510 (44%), Positives = 326/510 (63%), Gaps = 18/510 (3%) Query: 27 ILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKMIAEEVG 86 I DTTLRDGEQS G + +KLE ARQL +LGVD+IEAGFP +S D +VK IA E+ Sbjct: 6 IFDTTLRDGEQSLGITLNTHEKLEIARQLVRLGVDVIEAGFPASSPGDMNSVKTIAREIK 65 Query: 87 NCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLRKSKDQV 146 V I G++R KDI EAL+ A++PR+ T IA SP+HME KLR S +QV Sbjct: 66 GAV--------ICGLTRAVAKDIDACAEALRDAEQPRIHTGIAVSPVHMEKKLRLSPEQV 117 Query: 147 LETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDTVGIAMP 206 +E A VK A+ +D++F AEDA+RS+ FL +I +VI+AGAT + IPDTVG P Sbjct: 118 VEAAVAAVKHAKKY-VSDVEFYAEDASRSEPAFLAKILEKVIEAGATVVNIPDTVGYVTP 176 Query: 207 FEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTINGIGERAG 266 ++YG+LI+ + N I++AI++THCHNDLG+ATANT+ + GA Q+E TINGIGERAG Sbjct: 177 WQYGELISFLTKNVKNIDSAIISTHCHNDLGMATANTLAAVKAGASQVEGTINGIGERAG 236 Query: 267 NASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVGANAFLH 326 N + EEV+MA+ + L G+ G+ T+ I TS++V +G+ + HKA+VGANAF+H Sbjct: 237 NTALEEVMMAVYSQ--PSLYGVELGVKTKEIAATSRLVSGITGVPVPSHKAIVGANAFMH 294 Query: 327 ESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGYKLKDTE 386 SGIHQDG+LK + TYEII PE +G++R + IVL SGR AL++RLEELGY + + Sbjct: 295 ASGIHQDGVLKEKRTYEIIDPETVGILR---NKIVLSARSGRHALKHRLEELGYSPEQYD 351 Query: 387 VEGVFWQFKAVAEKKKRITDTDLRALVSNEAFNEQPIWKLGDLQVTCGTVGFSTATVKLF 446 VE V+ +F +A++KK + D DL AL+ I + ++ V +TATV L Sbjct: 352 VETVYKEFLQLADQKKEVFDEDLHALMGYTEKERNSI-SIKNISVATNGAATATATVSL- 409 Query: 447 SIDGSMHVACSIGTGPVDSAYKAINHIVKEPAKLVKYTLGAITEGIDATATTSVEISRGD 506 +++ + + G GPVD+ +KAI I KL Y L +++ G +A V++ G+ Sbjct: 410 AMNDQILTDAAYGNGPVDAVFKAIERITGITVKLEDYNLSSVSRGSEALGNAIVKVRYGE 469 Query: 507 TNHPVFSGTGGGTDVVVSSVDAYLSALNNM 536 + + G G DV+ ++ AY++AL+ + Sbjct: 470 SG--LVIGRGVSPDVIEATAKAYVNALSKI 497 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: 674 Number of extensions: 27 Number of successful extensions: 6 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: 501 Length adjustment: 35 Effective length of query: 505 Effective length of database: 466 Effective search space: 235330 Effective search space used: 235330 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