Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_028314083.1 G491_RS0107090 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_000429905.1:WP_028314083.1 Length = 516 Score = 432 bits (1111), Expect = e-125 Identities = 233/512 (45%), Positives = 334/512 (65%), Gaps = 18/512 (3%) Query: 25 VRILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKMIAEE 84 V I DTTLRDGEQSPGA M +K+ A +L LGVDI+EAGFP AS+ DF AV+ +A Sbjct: 5 VYIFDTTLRDGEQSPGATMNAKEKVRIASRLEALGVDIMEAGFPAASEGDFAAVQDVAAV 64 Query: 85 VGNCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLRKSKD 144 C + + G++R ++ DI AW A++HAK PR+ TFIATS IH+E+KL+ +++ Sbjct: 65 ---CQKSS-----VAGLARTSKSDIDKAWGAVQHAKHPRIHTFIATSDIHLEHKLKMNRE 116 Query: 145 QVLETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDTVGIA 204 QV+E A N VK+A+S D++F AED +RSD+++L ++F I AGATT+ +PDTVG A Sbjct: 117 QVVEAAVNAVKYAKSF-TDDVEFSAEDGSRSDRDYLCRVFEAAIAAGATTVNLPDTVGYA 175 Query: 205 MPFEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTINGIGER 264 +P E+ +L+ + +TP I AI++ HCHNDLGLAT+NT+ + GARQ EVT+NGIGER Sbjct: 176 IPHEFAELVKYVMDHTPNIHQAILSVHCHNDLGLATSNTLAAIQAGARQAEVTVNGIGER 235 Query: 265 AGNASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVGANAF 324 AGN S EEVVMA+ R + HT I T I S++V +G+ +QP+KA+VGANAF Sbjct: 236 AGNTSLEEVVMAMHTRPNYL--DFHTNIVTEQIHPASRLVRMITGIMVQPNKAIVGANAF 293 Query: 325 LHESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGYKLKD 384 HE+GIHQDG+LK+ TYEI+ PE +GL + + +VLGK SGR ALR+ L ++GY L D Sbjct: 294 AHEAGIHQDGVLKNPMTYEIMRPETVGLSK---NNMVLGKHSGRHALRSHLADMGYVLSD 350 Query: 385 TEVEGVFWQFKAVAEKKKRITDTDLRALVSNEAFNEQPIWKLGDLQVTCGTVGFSTATVK 444 E++ +F +FK +A+KKK + D DL ALVS + L L V+ GT TATV Sbjct: 351 EELQDLFIKFKDLADKKKHVVDEDLEALVSIGILRTSDKYSLDYLHVSAGTGVKPTATVG 410 Query: 445 LFSIDGSMHVACSIGTGPVDSAYKAINHIVKEPAKLVKYTLGAITEGIDATATTSVEISR 504 L +G + + G GP+D+A+ I + ++++++T+ A+T G DA +V + Sbjct: 411 L-KTNGDVLMGAEFGNGPIDAAFNTIAKMTGTTSEMLRFTVSALTGGTDAQGEVTVRLQE 469 Query: 505 GDTNHPVFSGTGGGTDVVVSSVDAYLSALNNM 536 G + G G D++ +S AY++ +N + Sbjct: 470 GKN---IALGRGVDPDIITASAKAYVNGINRL 498 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: 688 Number of extensions: 30 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: 516 Length adjustment: 35 Effective length of query: 505 Effective length of database: 481 Effective search space: 242905 Effective search space used: 242905 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