Align isocitrate lyase (EC 4.1.3.1) (characterized)
to candidate RR42_RS12200 RR42_RS12200 isocitrate lyase
Query= BRENDA::P9WKK7 (428 letters) >FitnessBrowser__Cup4G11:RR42_RS12200 Length = 430 Score = 605 bits (1559), Expect = e-177 Identities = 302/419 (72%), Positives = 348/419 (83%), Gaps = 2/419 (0%) Query: 10 AEQIQQEWDTNPRWKDVTRTYSAEDVVALQGSVVEEHTLARRGAEVLWEQLHDLEWVNAL 69 A +Q+EWDTNPRWK V R Y+A+DVV L+GSV EHTLARRGAE LW L+ +VN L Sbjct: 7 ARNLQKEWDTNPRWKGVARHYTADDVVRLRGSVQIEHTLARRGAEKLWHLLNTEPFVNTL 66 Query: 70 GALTGNMAVQQVRAGLKAIYLSGWQVAGDANLSGHTYPDQSLYPANSVPQVVRRINNALQ 129 GALTGN A+QQV+AGLKAIYLSGWQVAGDANL+G YPDQSLYPANSVPQVVRRINN Q Sbjct: 67 GALTGNQAMQQVKAGLKAIYLSGWQVAGDANLAGEMYPDQSLYPANSVPQVVRRINNTFQ 126 Query: 130 RADQIAKIEGDTSVENWLAPIVADGEAGFGGALNVYELQKALIAAGVAGSHWEDQLASEK 189 RADQI EG + + APIVAD EAGFGG LN +EL K++I AG AG H+EDQLAS K Sbjct: 127 RADQIQWSEGKGDTD-FFAPIVADAEAGFGGVLNAFELMKSMIDAGAAGVHFEDQLASVK 185 Query: 190 KCGHLGGKVLIPTQQHIRTLTSARLAADVADVPTVVIARTDAEAATLITSDVDERDQPFI 249 KCGH+GGKVL+PT++ + LT+ARLAADV+ VPT+VIARTDAEAA L+TSDVDERD+PF Sbjct: 186 KCGHMGGKVLVPTREAVAKLTAARLAADVSGVPTLVIARTDAEAADLLTSDVDERDRPFC 245 Query: 250 TGERTREGFYRTKNGIEPCIARAKAYAPFADLIWMETGTPDLEAARQFSEAVKAEYPDQM 309 TGERT EGFYR K GIE I+RA AYA ADL+W ETG PDLE A++F+EAV A++P +M Sbjct: 246 TGERTVEGFYRVKPGIEQSISRALAYAEVADLVWCETGKPDLEFAKKFAEAVHAKFPGKM 305 Query: 310 LAYNCSPSFNWKKHLDDATIAKFQKELAAMGFKFQFITLAGFHALNYSMFDLAYGYAQNQ 369 LAYNCSPSFNWKK+LDDATIAKFQKEL AMG+KFQFITLAGFH+LNYSMF+LAYGYA+N Sbjct: 306 LAYNCSPSFNWKKNLDDATIAKFQKELGAMGYKFQFITLAGFHSLNYSMFNLAYGYARNH 365 Query: 370 MSAYVELQEREFAAEERGYTATKHQREVGAGYFDRIATTVD-PNSSTTALTGSTEEGQF 427 MSA+VELQE EF A E+G+TA KHQREVG GYFD + T++ SSTTAL GSTE+ QF Sbjct: 366 MSAFVELQENEFTAAEKGFTAVKHQREVGTGYFDAVTQTIEGGQSSTTALKGSTEDEQF 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: 632 Number of extensions: 19 Number of successful extensions: 3 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: 430 Length adjustment: 32 Effective length of query: 396 Effective length of database: 398 Effective search space: 157608 Effective search space used: 157608 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 Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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