Align isocitrate lyase (EC 4.1.3.1) (characterized)
to candidate BWI76_RS01665 BWI76_RS01665 isocitrate lyase
Query= BRENDA::P9WKK7 (428 letters) >FitnessBrowser__Koxy:BWI76_RS01665 Length = 434 Score = 513 bits (1320), Expect = e-150 Identities = 264/427 (61%), Positives = 326/427 (76%), Gaps = 11/427 (2%) Query: 11 EQIQQEWDTNPRWKDVTRTYSAEDVVALQGSVVEEHTLARRGAEVLWEQLHDLE---WVN 67 E++ +EW T PRW+ +TR YSAEDVV L+GSV E TLA+ GA +W LH ++N Sbjct: 9 EELNKEW-TKPRWEGITRPYSAEDVVKLRGSVNPECTLAQLGAAKMWRLLHGEAKKGYIN 67 Query: 68 ALGALTGNMAVQQVRAGLKAIYLSGWQVAGDANLSGHTYPDQSLYPANSVPQVVRRINNA 127 +LGALTG A+QQ +AG++AIYLSGWQVA DANL+ YPDQSLYPANSVP VV RINN Sbjct: 68 SLGALTGGQALQQAKAGIEAIYLSGWQVAADANLASSMYPDQSLYPANSVPAVVDRINNT 127 Query: 128 LQRADQI---AKIE-GDTSVENWLAPIVADGEAGFGGALNVYELQKALIAAGVAGSHWED 183 +RADQI A IE D ++ PIVAD EAGFGG LN +EL K++I AG A H+ED Sbjct: 128 FRRADQIQWSAGIELNDPRYTDYFLPIVADAEAGFGGVLNAFELMKSMIEAGAAAVHFED 187 Query: 184 QLASEKKCGHLGGKVLIPTQQHIRTLTSARLAADVADVPTVVIARTDAEAATLITSDVDE 243 QLAS KKCGH+GGKVL+PTQ+ I+ L +ARLAADV VPT+VIARTDA+AA LITSD D Sbjct: 188 QLASVKKCGHMGGKVLVPTQEAIQKLVAARLAADVMGVPTLVIARTDADAADLITSDCDP 247 Query: 244 RDQPFITGERTREGFYRTKNGIEPCIARAKAYAPFADLIWMETGTPDLEAARQFSEAVKA 303 D+ FITG+RT EGF+RT GIE I+R AYAP+ADL+W ET TPDLE A++F++A+ A Sbjct: 248 YDRQFITGDRTSEGFFRTHAGIEQAISRGLAYAPYADLVWCETSTPDLELAKRFADAIHA 307 Query: 304 EYPDQMLAYNCSPSFNWKKHLDDATIAKFQKELAAMGFKFQFITLAGFHALNYSMFDLAY 363 +YP ++LAYNCSPSFNW+K LDD TIA FQ++LA MG+K+QFITLAG H++ ++MFDLA+ Sbjct: 308 KYPGKLLAYNCSPSFNWQKKLDDKTIASFQQQLADMGYKYQFITLAGIHSMWFNMFDLAH 367 Query: 364 GYAQNQ-MSAYVE-LQEREFAAEERGYTATKHQREVGAGYFDRIATTVD-PNSSTTALTG 420 YAQ + M YVE +Q+ EFAA + GYT HQ+EVG GYFD++ T + SS TALTG Sbjct: 368 AYAQGEGMKHYVEKVQQPEFAAAKDGYTFVSHQQEVGTGYFDKVTTIIQGGTSSVTALTG 427 Query: 421 STEEGQF 427 STEE QF Sbjct: 428 STEESQF 434 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: 600 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: 434 Length adjustment: 32 Effective length of query: 396 Effective length of database: 402 Effective search space: 159192 Effective search space used: 159192 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