Align isocitrate lyase (EC 4.1.3.1) (characterized)
to candidate SMc00768 SMc00768 isocitrate lyase
Query= BRENDA::P9WKK7 (428 letters) >FitnessBrowser__Smeli:SMc00768 Length = 429 Score = 548 bits (1412), Expect = e-160 Identities = 277/410 (67%), Positives = 319/410 (77%), Gaps = 4/410 (0%) Query: 22 RWKDVTRTYSAEDVVALQGSVVEEHTLARRGAEVLWEQLHDLEWVNALGALTGNMAVQQV 81 R+ + R YSAEDV L+GSV ++LA GA LW+ +H+ ++VNALGAL+GN A+Q V Sbjct: 15 RFDGIERPYSAEDVKRLRGSVEIRYSLAEMGANRLWKLIHEEDFVNALGALSGNQAMQMV 74 Query: 82 RAGLKAIYLSGWQVAGDANLSGHTYPDQSLYPANSVPQVVRRINNALQRADQIAKIEGD- 140 RAGLKAIYLSGWQVA DAN + YPDQSLYPAN+ P++ +RIN LQRADQI EG Sbjct: 75 RAGLKAIYLSGWQVAADANTASAMYPDQSLYPANAAPELAKRINRTLQRADQIETAEGKG 134 Query: 141 TSVENWLAPIVADGEAGFGGALNVYELQKALIAAGVAGSHWEDQLASEKKCGHLGGKVLI 200 SVE W APIVAD EAGFGG LN +E+ KA I AG AG H+EDQLASEKKCGHLGGKVLI Sbjct: 135 LSVETWFAPIVADAEAGFGGPLNAFEIMKAFIEAGAAGVHYEDQLASEKKCGHLGGKVLI 194 Query: 201 PTQQHIRTLTSARLAADVADVPTVVIARTDAEAATLITSDVDERDQPFITGE--RTREGF 258 PT HIR L +ARLAADV PT+VIARTDAEAA L+TSD+DERD+PF+ + RT EGF Sbjct: 195 PTAAHIRNLNAARLAADVMGTPTLVIARTDAEAAKLLTSDIDERDRPFVDYDAGRTVEGF 254 Query: 259 YRTKNGIEPCIARAKAYAPFADLIWMETGTPDLEAARQFSEAVKAEYPDQMLAYNCSPSF 318 Y+ KNGIEPCIARA AYAP DLIW ET PDLE AR+F+E V +P ++LAYNCSPSF Sbjct: 255 YQVKNGIEPCIARAIAYAPHCDLIWCETSKPDLEQARKFAEGVHKAHPGKLLAYNCSPSF 314 Query: 319 NWKKHLDDATIAKFQKELAAMGFKFQFITLAGFHALNYSMFDLAYGYAQNQMSAYVELQE 378 NWKK+LDDATIAKFQ+EL AMG+KFQFITLAGFH LNY MF+LA GY QM+AY ELQE Sbjct: 315 NWKKNLDDATIAKFQRELGAMGYKFQFITLAGFHQLNYGMFELARGYRDRQMAAYSELQE 374 Query: 379 REFAAEERGYTATKHQREVGAGYFDRIATTV-DPNSSTTALTGSTEEGQF 427 EFAAE GYTATKHQREVG GYFD ++ + SSTTA+ STE QF Sbjct: 375 AEFAAEANGYTATKHQREVGTGYFDAVSVAITGGQSSTTAMKESTEHDQF 424 Lambda K H 0.316 0.130 0.384 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: 574 Number of extensions: 20 Number of successful extensions: 4 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: 428 Length of database: 429 Length adjustment: 32 Effective length of query: 396 Effective length of database: 397 Effective search space: 157212 Effective search space used: 157212 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: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
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