Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_013009813.1 DACET_RS02375 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_000025725.1:WP_013009813.1 Length = 519 Score = 450 bits (1157), Expect = e-131 Identities = 237/510 (46%), Positives = 333/510 (65%), Gaps = 14/510 (2%) Query: 25 VRILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKMIAEE 84 V I DTTLRDGEQ+PG +M +K++ A QL +LGVD++EAGFP +S DF AV +A+ Sbjct: 6 VIIFDTTLRDGEQAPGFSMNTDEKIQLALQLERLGVDVMEAGFPISSPGDFEAVTRVAKV 65 Query: 85 VGNCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLRKSKD 144 + N + G+ R NEKDI+ W+AL+HA RPR+ TFIATS IH+++KL+K+++ Sbjct: 66 IKNSG--------VAGLCRANEKDISVGWDALQHAVRPRIHTFIATSDIHLQHKLKKTRE 117 Query: 145 QVLETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDTVGIA 204 + LE A VKFAR+L C D++F AEDA RSD ++L Q+ VI AGA T+ +PDTVG Sbjct: 118 EALEIAVKAVKFARNL-CDDVEFSAEDAMRSDVDYLCQVVEAVIAAGANTVNLPDTVGYK 176 Query: 205 MPFEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTINGIGER 264 MPFE K+I+++ P ++ A ++ HCHNDLGL+ AN++ GA Q+E TINGIGER Sbjct: 177 MPFEIDKVISEVINRVPNVDKARISVHCHNDLGLSVANSLMAVNAGASQIECTINGIGER 236 Query: 265 AGNASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVGANAF 324 AGN S EEVVM LT R D+ + G+ T I + SKM+ +G+ +QP+KA+VG NAF Sbjct: 237 AGNCSLEEVVMGLTVRK-DVFDDIEIGVKTNEIYRASKMLTTITGVGVQPNKAIVGKNAF 295 Query: 325 LHESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGYKLKD 384 HE+GIHQDGMLK+R TYEI++PE +G + ++VLGK SGR A R+++LGY++++ Sbjct: 296 AHEAGIHQDGMLKNRTTYEIMTPESVGYPST---SLVLGKHSGRHAFVQRIKDLGYEIEN 352 Query: 385 TEVEGVFWQFKAVAEKKKRITDTDLRALVSNEAFNEQPIWKLGDLQVTCGTVGFSTATVK 444 ++ F +FK +A+KKK + D D+ +++ N+A +EQ + + + + G TAT+K Sbjct: 353 DAMQSAFDEFKILADKKKEVFDEDIESIIFNQAKDEQFAYVMESVNILSGDTAIPTATIK 412 Query: 445 LFSIDGSMHVACSIGTGPVDSAYKAINHIVKEPAKLVKYTLGAITEGIDATATTSVEISR 504 L DG+ V S G GPVD+ KAI I KL Y + A+T G DA + Sbjct: 413 LADKDGNEFVDASTGDGPVDAVMKAIERIAGVGGKLKSYQIKALTAGKDAQGEVVLSAEF 472 Query: 505 GDTNHPVFSGTGGGTDVVVSSVDAYLSALN 534 + + V G G TDVVV+S AYL ALN Sbjct: 473 EECGYDV-RGRGSDTDVVVASAKAYLDALN 501 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: 628 Number of extensions: 25 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: 519 Length adjustment: 35 Effective length of query: 505 Effective length of database: 484 Effective search space: 244420 Effective search space used: 244420 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