Align 2-isopropylmalate synthase (EC 2.3.3.13) (characterized)
to candidate WP_066325976.1 BLR17_RS13745 2-isopropylmalate synthase
Query= reanno::Cola:Echvi_3833 (390 letters) >NCBI__GCF_900100165.1:WP_066325976.1 Length = 391 Score = 567 bits (1461), Expect = e-166 Identities = 280/388 (72%), Positives = 330/388 (85%) Query: 1 MDKRQVLIFDTTLRDGEQVPGCKLNTPQKIEIARQLESLGVDVIEAGFPISSPGDFKSVV 60 M++ +V IFDTTLRDGEQVPGCKL+T QK+ IA +L+++GVD+IEAGFP+SSPGDF SV Sbjct: 1 MNRDKVQIFDTTLRDGEQVPGCKLDTNQKLVIAERLDNMGVDIIEAGFPVSSPGDFLSVT 60 Query: 61 EISKSVSEPIICGLSRGVAKDIEVAAEALKYAKRPRIHTGIGTSPSHIKYKFKSTPDQIL 120 EISK V +CGL+R V DI+VAA ALK+AKRPRIHTGIGTS SHI +K ++T + I+ Sbjct: 61 EISKIVKNATVCGLTRAVKNDIDVAAAALKHAKRPRIHTGIGTSESHILHKLQTTREDII 120 Query: 121 ERAVAAVKHAKSFVEDVEFYAEDAGRTDNEYLARICEAVVKAGATVLNIPDTTGYCLPDE 180 RA AAV HAKS+VEDVEFYAEDAGRTDN +LA++CE V+K+GATVLNIPDTTGYCLP+E Sbjct: 121 ARAKAAVAHAKSYVEDVEFYAEDAGRTDNAFLAQVCEEVIKSGATVLNIPDTTGYCLPEE 180 Query: 181 YGAKIKYLMDNVKGIENVIISAHCHNDLGLATANSISAVMNGARQIECTINGIGERAGNT 240 YGAKIKYL +NVKGIENV IS HCHNDLG+ATANSIS +NGARQIECTINGIGERAGNT Sbjct: 181 YGAKIKYLKENVKGIENVTISCHCHNDLGMATANSISGAINGARQIECTINGIGERAGNT 240 Query: 241 SLEEVAMIMKQHPRLNVYNKINSRLLNPISRLVSERMGMHVQPNKAIVGSNAFAHSSGIH 300 +LEEV MI KQHP LN+Y I+++ LN +SRLVSE MGM VQPNKAIVG+NAFAHSSGIH Sbjct: 241 ALEEVVMIFKQHPDLNLYTDIDTKQLNEMSRLVSESMGMMVQPNKAIVGANAFAHSSGIH 300 Query: 301 QDGVIKNRETYEIIDPEEVGVTESMIVLTARSGRAALAFRLHKIGYTITKLQLDDIYQLF 360 QDGVIKNR TYEIIDP +VGV ES IVLTARSGRAALA+R K+GY +TK QLD +Y F Sbjct: 301 QDGVIKNRATYEIIDPLDVGVNESSIVLTARSGRAALAYRAKKVGYELTKNQLDVVYVEF 360 Query: 361 LEHADMKKEITDEDLHEIMKVSSVPGNV 388 L+ AD+KKEI D+D+H I+ S + G++ Sbjct: 361 LKFADVKKEILDDDIHLIIAASKIEGDL 388 Lambda K H 0.317 0.134 0.375 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: 495 Number of extensions: 12 Number of successful extensions: 1 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: 390 Length of database: 391 Length adjustment: 31 Effective length of query: 359 Effective length of database: 360 Effective search space: 129240 Effective search space used: 129240 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 (21.6 bits) S2: 50 (23.9 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