Align Probable 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate WP_013257767.1 DEBA_RS04730 citramalate synthase
Query= curated2:Q8TYB1 (499 letters) >NCBI__GCF_000143965.1:WP_013257767.1 Length = 536 Score = 213 bits (542), Expect = 1e-59 Identities = 172/529 (32%), Positives = 258/529 (48%), Gaps = 47/529 (8%) Query: 2 PDR--VRIFDTTLRDGEQTPGVSLTVEEKVEIARKLDEFGVDTIEAGFPVASEGEFEAVR 59 PD+ V I+DTTLRDG Q G L+V++K+++A++LD GV IE G+P S + Sbjct: 5 PDKRVVEIYDTTLRDGTQAAGFVLSVDDKLKVAQRLDHLGVHYIEGGWP-GSNPRDKQFF 63 Query: 60 AIAGEELDAEICGLA---------RCVKGDIDAA--IDADVDCVHVFIATSDIHLRYKLE 108 A AGE L + L R + D + A + A D V + T D H+ +L Sbjct: 64 ARAGE-LRLKTAKLVAFGSTHHANRRPENDQNLADLLGAGTDVVTMVGKTWDRHVTIQLG 122 Query: 109 MSREEALERAIEGVEYASDHGVTVEFSAE---DATRTDRDYLLEVYKATVEAGADRVNVP 165 + E L + V Y S H + V F AE D + +R+Y L KA E GA + + Sbjct: 123 VPLERNLAMIADSVAYLSRHHIQVFFDAEHFFDGLKHNREYTLACLKAAAEGGAKCLVLC 182 Query: 166 DTVGVMTPPEMYRLTAEVVDAVD-VPVSVHCHNDFGMAVANSLAAVEAGAEQVHVTVNGI 224 DT G P ++ T V + + V VH HND +AVANSLAAVEAGA QV T+NG+ Sbjct: 183 DTNGGSLPGQVAEATRLVRQTLPGLAVGVHTHNDAELAVANSLAAVEAGASQVQGTINGV 242 Query: 225 GERAGNASLEQVVMALKALYDIEL--DVRTEMLVELSRLVERLTGVVVPPNTPIVGENAF 282 GER GNA+L +V AL+ + + R +L + +R V L P P VG AF Sbjct: 243 GERCGNANLCSIVAALELKMGLRALPEGRLPLLTDTARFVLELANQQPRPFAPYVGRAAF 302 Query: 283 AHESGIHSHGVIKKAETYEPIRPEDVGHRRRIVLGKHAGRHAIKKKLEEMGIEVTEEQ-- 340 H+ G+H V K YE + PE VG+ RR ++ AG+ AI +K +MG+++ + Sbjct: 303 GHKGGLHISAVEKDPALYEHVSPEAVGNDRRYLISDLAGKAAILRKARDMGLDLADNDPA 362 Query: 341 LDEIVRRVKELGDKG--KRVTEDDLEAIARDVVGEVPESEAAVKLEEIAVMTGNKF---- 394 L ++ +K +KG E E + V+G + +L + V T + Sbjct: 363 LGRMLEELKAQENKGYVYEAAEASFELLINRVLG---REKTYFQLMDFRVHTHKEANNIL 419 Query: 395 -------TPTASVRVYLDGEEHEAASTGVGSVDAAIRALREAIEELGM-----DVELKEY 442 A+V V +DG A+ G G V+A RA+R+A+ LG +++L +Y Sbjct: 420 GCKAPGPVSEATVMVLVDGRVRHTAAVGNGPVNALDRAMRKAL--LGFYPQLAEMQLVDY 477 Query: 443 RLEAITGGTDALAEVTVRLEDEDGNVTTAR-GAAEDIVMASVKAFVRGV 490 ++ ++ A V V +E DG G + D++ AS +A + Sbjct: 478 KVRVLSSADGTAARVRVLIESSDGRSRWGTVGVSFDVLEASWQALSESI 526 Lambda K H 0.315 0.133 0.364 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: 487 Number of extensions: 22 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: 499 Length of database: 536 Length adjustment: 35 Effective length of query: 464 Effective length of database: 501 Effective search space: 232464 Effective search space used: 232464 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 (21.5 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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