Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_078430192.1 BK574_RS22745 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_002019605.1:WP_078430192.1 Length = 511 Score = 413 bits (1061), Expect = e-120 Identities = 232/514 (45%), Positives = 324/514 (63%), Gaps = 18/514 (3%) Query: 25 VRILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKMIAEE 84 + + DTTLRDGEQS G + +K+E A+QL +LGVD++EAGFP AS DF +VK IA+ Sbjct: 4 INVFDTTLRDGEQSAGVNLNFEEKMEIAKQLERLGVDVMEAGFPAASPGDFNSVKAIADT 63 Query: 85 VGNCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLRKSKD 144 + C + G+SR E DI AW+ALK PRL FIATSPIHME+KLR + D Sbjct: 64 IKGCS--------VIGLSRSVESDIDAAWDALKGGAEPRLHVFIATSPIHMEHKLRLTPD 115 Query: 145 QVLETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDTVGIA 204 QV+E A VK+A + IQ+ AEDA RSD +FL +I +VI AGA+ + IPDTVG Sbjct: 116 QVVENAVAAVKYAATR-FPKIQWSAEDACRSDLDFLVRIIEQVIDAGASVINIPDTVGYI 174 Query: 205 MPFEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTINGIGER 264 P E + + +K N ++ AI++THCH+DLGLATAN++ GA Q+E TINGIGER Sbjct: 175 TPKEITHIFSYLKNNVRNMDKAILSTHCHDDLGLATANSLAAIEAGADQVECTINGIGER 234 Query: 265 AGNASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVGANAF 324 AGNAS EE+ +AL R + +TGI + I +TS +V K +G+ + +KA+VG NAF Sbjct: 235 AGNASLEEIAVALHIR--NDFYKANTGITLKEIKRTSSLVSKLTGMIVPNNKAVVGNNAF 292 Query: 325 LHESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGYKLKD 384 HESGIHQDG+LK + TYEII+PE +G+ + +VLGK SGR A +++++ELGY D Sbjct: 293 AHESGIHQDGVLKEKSTYEIITPELVGV---SSNRMVLGKHSGRHAFKDKIKELGYTASD 349 Query: 385 TEVEGVFWQFKAVAEKKKRITDTDLRALVSNEAFNEQ-PIWKLGDLQVTCGTVGFSTATV 443 ++ VF FK +A+KKK IT+ D+ AL++ E +++ LQV GT TAT+ Sbjct: 350 EQLNKVFKAFKELADKKKEITEDDIFALMTEEKIGAAVQYYEVDSLQVNYGTANIPTATI 409 Query: 444 KLFSIDGSMHVACSIGTGPVDSAYKAINHIVKEPAKLVKYTLGAITEGIDATATTSVEIS 503 + DG + + G+G V++ Y + I+ P KL+ Y + +IT G DA A V++ Sbjct: 410 TMKMPDGEVVQEAATGSGSVEAIYNTLERIIASPVKLLDYRIQSITGGRDALAEVYVKVR 469 Query: 504 RGDTNHPVFSGTGGGTDVVVSSVDAYLSALNNML 537 T SG G DV+ +S AY++A+N +L Sbjct: 470 FDGTE---TSGRGTAHDVLEASARAYINAVNRVL 500 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: 634 Number of extensions: 32 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: 511 Length adjustment: 35 Effective length of query: 505 Effective length of database: 476 Effective search space: 240380 Effective search space used: 240380 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