Align Probable methanogen homoaconitase large subunit; HACN; EC 4.2.1.114; Homoaconitate hydratase (uncharacterized)
to candidate Synpcc7942_1898 Synpcc7942_1898 isopropylmalate isomerase large subunit
Query= curated2:O27668 (428 letters) >FitnessBrowser__SynE:Synpcc7942_1898 Length = 468 Score = 221 bits (563), Expect = 4e-62 Identities = 154/442 (34%), Positives = 219/442 (49%), Gaps = 61/442 (13%) Query: 30 VDLAMTHDGTSPPTIRTFRDIASRGGPARVWDPERIVMVFDHNVPANTIGA------AEF 83 + L + H+ TSP RD RG + P R V DH VP AE Sbjct: 28 IGLHLIHEVTSPQAFSMLRD---RGLTVKF--PGRTVATVDHIVPTENQARPFADSLAEE 82 Query: 84 QRVTREF-AREQGI--VNIFQNAAGICHQVLPERGFVRPGMVIVGADSHTCTYGAFGAFA 140 VT E RE GI NI + GI H + PE+G +PGM I DSHT T+GAFGA A Sbjct: 83 MIVTLERNCRENGIRFYNIGSGSQGIVHVIAPEQGLTQPGMTIACGDSHTSTHGAFGAIA 142 Query: 141 TGMGATDMAMVFATGKTWFMVPEAMRIEVTGEPEGHVYAKDVILHIIGEIGVDGATYRSV 200 G+G + + V A+ + +IEV GE + VYAKDVILHII ++GV G + Sbjct: 143 FGIGTSQVRDVLASQTLALSKLKVRKIEVNGELQPGVYAKDVILHIIRKLGVKGGVGYAY 202 Query: 201 EFTGDTIESMDVSGRMTICNMAVEMGAKNGIMEPNRQTLDYVRARTGREF---------- 250 EF G T +M + RMT+CNMA+E GA+ G + P++ T DY++ GREF Sbjct: 203 EFAGSTFAAMSMEERMTVCNMAIEGGARCGYVNPDQITYDYLQ---GREFAPQGEAWDRA 259 Query: 251 ----RVYSSDEDSQYLEDHHFDVSDLEPQVA----------------CPD---DVD---- 283 S+ D++Y + FD +++ P V PD D D Sbjct: 260 IAWWESLRSEADAEYDDVVVFDAAEIAPTVTWGITPGQGIGITETIPTPDSLLDEDRAVA 319 Query: 284 -------NVYPVHRVEGTHIDEAFLGSCTNGRYEDLKIAAEVIGDRRVHEDVRFIVSPAS 336 ++ P ++GT +D F+GSCTNGR DL+ AA+V R+V ++ V P S Sbjct: 320 AEAYSYMDLEPGAPLQGTKVDVCFIGSCTNGRLSDLREAAKVAQGRKVAAGIKAFVVPGS 379 Query: 337 REIYLKALEDGIIETFIRAGAIVCNPGCGPCLGAHMGVLAPGEVSIATTNRNFRGRMGDP 396 + +A +G+ + F AG GC CL + L ++S +++NRNF+GR G Sbjct: 380 ERVKQQAEAEGLDQIFTAAGFEWRQAGCSMCLAMNPDKLEGRQISASSSNRNFKGRQGSA 439 Query: 397 ASSVYLANPAVVAESAIEGVIS 418 + L +PA+VA +AI G ++ Sbjct: 440 SGRTLLMSPAMVAAAAIAGEVT 461 Lambda K H 0.320 0.137 0.408 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: 535 Number of extensions: 25 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 428 Length of database: 468 Length adjustment: 33 Effective length of query: 395 Effective length of database: 435 Effective search space: 171825 Effective search space used: 171825 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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