Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_084276501.1 B8779_RS09685 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_900176045.1:WP_084276501.1 Length = 516 Score = 432 bits (1111), Expect = e-125 Identities = 241/513 (46%), Positives = 330/513 (64%), Gaps = 17/513 (3%) Query: 25 VRILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKMIAEE 84 V+I DTTLRDGEQSPGA+M +K++ A+QL KLGVDIIEAGF AS DF A++ I+E Sbjct: 5 VKIFDTTLRDGEQSPGASMNTEEKIQIAKQLEKLGVDIIEAGFAAASPGDFEAIRKISEV 64 Query: 85 VGNCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLRKSKD 144 V + ++R EKDI A EA+ AK R+ TFIATSPIHM+YKLR + Sbjct: 65 VNKST--------VCSLARALEKDIKAAGEAIAPAKFKRIHTFIATSPIHMKYKLRMEPE 116 Query: 145 QVLETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDTVGIA 204 +V++ A VK+A++ D++F EDA RS+ FL +I VI+AGA T+ IPDTVG Sbjct: 117 EVIKRAIEAVKYAKTF-VNDVEFSCEDAGRSEMAFLKEIIAAVIEAGAKTINIPDTVGYR 175 Query: 205 MPFEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTINGIGER 264 P E G++I ++K E AI++ HCHNDLGLA AN++ GARQ+E TING+GER Sbjct: 176 FPHEMGEMIKELKDFIG--ERAIISVHCHNDLGLAVANSLYSVLNGARQVECTINGLGER 233 Query: 265 AGNASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVGANAF 324 AGNA+ EE+VMA+ R DI G+ T INT+ I TS++V +G+ QP+KA+VG NAF Sbjct: 234 AGNAALEEIVMAIKTRK-DIFDGIDTNINTKEIYPTSRLVAAITGIEPQPNKAIVGKNAF 292 Query: 325 LHESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGYKLKD 384 HESGIHQDG+LKH+ TYEI+ EDIGL R + IVLGK SGR A + R+E+LG+ L + Sbjct: 293 AHESGIHQDGVLKHQETYEIMRAEDIGLDR---NAIVLGKHSGRHAFKKRIEDLGFTLSE 349 Query: 385 TEVEGVFWQFKAVAEKKKRITDTDLRALVSNEAFNEQPIWKLGDLQVTCGTVGFSTATVK 444 E+ F +FK +A+KKK ITD D+R L++NE + ++KL LQ++ + G +A V Sbjct: 350 EEINKAFERFKVLADKKKEITDDDIRMLITNEIASAPEVYKLKKLQISDCSEGVPSAAVT 409 Query: 445 LFSIDGSMHVACSIGTGPVDSAYKAINHIVKEPAKLVKYTLGAITEGIDATATTSVEISR 504 + DG IG G +D+ +K I+ I L Y + A+++G DA A V++ Sbjct: 410 I-EFDGKEITDAGIGDGTIDAIFKTIDRISGYKGTLNDYQVAAVSKGKDALAKVVVKVV- 467 Query: 505 GDTNHPVFSGTGGGTDVVVSSVDAYLSALNNML 537 D P G G D +++S AY+SALN+ + Sbjct: 468 FDEKKPAVIGHGLSIDTMIASAKAYVSALNSYI 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: 659 Number of extensions: 29 Number of successful extensions: 8 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