Align isocitrate lyase (EC 4.1.3.1) (characterized)
to candidate 6938260 Sama_2380 isocitrate lyase (RefSeq)
Query= BRENDA::P9WKK7 (428 letters) >lcl|FitnessBrowser__SB2B:6938260 Sama_2380 isocitrate lyase (RefSeq) Length = 439 Score = 526 bits (1355), Expect = e-154 Identities = 267/435 (61%), Positives = 331/435 (76%), Gaps = 10/435 (2%) Query: 4 VGTPKSAEQIQQEWDTNPRWKDVTRTYSAEDVVALQGSVVEEHTLARRGAEVLWEQLHD- 62 + + + ++++W NPRWK V R Y+AE+VV+L+GS V E+T+A+RGA LW+ ++ Sbjct: 5 ISRQEQIDALKKDWAENPRWKGVRRPYTAEEVVSLRGSFVPENTVAQRGAAKLWDLVNGG 64 Query: 63 --LEWVNALGALTGNMAVQQVRAGLKAIYLSGWQVAGDANLSGHTYPDQSLYPANSVPQV 120 +VN+LGALTG AVQQ +AG++AIYLSGWQVA DANL+G YPDQSLYPANSVP V Sbjct: 65 AKKGYVNSLGALTGGQAVQQAKAGIEAIYLSGWQVAADANLAGTMYPDQSLYPANSVPAV 124 Query: 121 VRRINNALQRADQIAKIEG----DTSVENWLAPIVADGEAGFGGALNVYELQKALIAAGV 176 V RINN+ +RADQI G D ++ PIVAD EAGFGG LN YEL K++I AG Sbjct: 125 VGRINNSFRRADQIQWSNGVGPEDDKFVDYFLPIVADAEAGFGGVLNAYELMKSMIDAGA 184 Query: 177 AGSHWEDQLASEKKCGHLGGKVLIPTQQHIRTLTSARLAADVADVPTVVIARTDAEAATL 236 AG H+EDQLAS KKCGH+GGKVL+PTQ+ ++ L +ARLAADV+ V T+VIARTDA AA L Sbjct: 185 AGVHFEDQLASVKKCGHMGGKVLVPTQEAVQKLVAARLAADVSGVETLVIARTDANAADL 244 Query: 237 ITSDVDERDQPFITGERTREGFYRTKNGIEPCIARAKAYAPFADLIWMETGTPDLEAARQ 296 +TSD D D FITGERT EGFYR + G++ IAR AYAP+ADLIW ET PDLE AR+ Sbjct: 245 LTSDCDPYDSDFITGERTSEGFYRVRAGLDQAIARGLAYAPYADLIWCETAKPDLEEARR 304 Query: 297 FSEAVKAEYPDQMLAYNCSPSFNWKKHLDDATIAKFQKELAAMGFKFQFITLAGFHALNY 356 F+EA+ A+YPDQ+LAYNCSPSFNWKK+LDDATIAKFQ+ L+ MG+K+QFITLAG H + + Sbjct: 305 FAEAIHAKYPDQLLAYNCSPSFNWKKNLDDATIAKFQQALSDMGYKYQFITLAGIHNMWF 364 Query: 357 SMFDLAYGYAQNQ-MSAYVE-LQEREFAAEERGYTATKHQREVGAGYFDRIATTVDPN-S 413 +MFDLAY YA+ + M YVE +QE EFAA +GYT HQ+EVG GYFD++ + S Sbjct: 365 NMFDLAYDYARGEGMKHYVEKVQEAEFAAASKGYTFVAHQQEVGTGYFDKMTNIIQGGAS 424 Query: 414 STTALTGSTEEGQFH 428 S TALTGSTEE QFH Sbjct: 425 SVTALTGSTEEEQFH 439 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: 593 Number of extensions: 20 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: 428 Length of database: 439 Length adjustment: 32 Effective length of query: 396 Effective length of database: 407 Effective search space: 161172 Effective search space used: 161172 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