Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_066325976.1 BLR17_RS13745 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_900100165.1:WP_066325976.1 Length = 391 Score = 338 bits (867), Expect = 2e-97 Identities = 188/394 (47%), Positives = 259/394 (65%), Gaps = 15/394 (3%) Query: 21 NPTYVRILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKM 80 N V+I DTTLRDGEQ PG + QKL A +L +GVDIIEAGFP +S DF++V Sbjct: 2 NRDKVQIFDTTLRDGEQVPGCKLDTNQKLVIAERLDNMGVDIIEAGFPVSSPGDFLSVTE 61 Query: 81 IAEEVGNCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLR 140 I++ V N + G++R + DI A ALKHAKRPR+ T I TS H+ +KL+ Sbjct: 62 ISKIVKNAT--------VCGLTRAVKNDIDVAAAALKHAKRPRIHTGIGTSESHILHKLQ 113 Query: 141 KSKDQVLETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDT 200 +++ ++ A+ V A+S D++F AEDA R+D FL Q+ EVIK+GAT L IPDT Sbjct: 114 TTREDIIARAKAAVAHAKSY-VEDVEFYAEDAGRTDNAFLAQVCEEVIKSGATVLNIPDT 172 Query: 201 VGIAMPFEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTING 260 G +P EYG I +K N GIEN ++ HCHNDLG+ATAN+I GA GARQ+E TING Sbjct: 173 TGYCLPEEYGAKIKYLKENVKGIENVTISCHCHNDLGMATANSISGAINGARQIECTING 232 Query: 261 IGERAGNASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVG 320 IGERAGN + EEVVM + D+ L+T I+T+ + + S++V + G+ +QP+KA+VG Sbjct: 233 IGERAGNTALEEVVMIFK-QHPDL--NLYTDIDTKQLNEMSRLVSESMGMMVQPNKAIVG 289 Query: 321 ANAFLHESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGY 380 ANAF H SGIHQDG++K+R TYEII P D+G+ S +IVL SGR AL R +++GY Sbjct: 290 ANAFAHSSGIHQDGVIKNRATYEIIDPLDVGVNES---SIVLTARSGRAALAYRAKKVGY 346 Query: 381 KLKDTEVEGVFWQFKAVAEKKKRITDTDLRALVS 414 +L +++ V+ +F A+ KK I D D+ +++ Sbjct: 347 ELTKNQLDVVYVEFLKFADVKKEILDDDIHLIIA 380 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: 504 Number of extensions: 25 Number of successful extensions: 5 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: 391 Length adjustment: 33 Effective length of query: 507 Effective length of database: 358 Effective search space: 181506 Effective search space used: 181506 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: 51 (24.3 bits)
This GapMind analysis is from Jul 26 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