Align Probable 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate WP_053767939.1 BVI061214_RS07990 citramalate synthase
Query= curated2:Q8TYB1 (499 letters) >NCBI__GCF_001280255.1:WP_053767939.1 Length = 526 Score = 229 bits (585), Expect = 1e-64 Identities = 175/512 (34%), Positives = 262/512 (51%), Gaps = 31/512 (6%) Query: 5 VRIFDTTLRDGEQTPGVSLTVEEKVEIARKLDEFGVDTIEAGFPVASEGEFEAVRAIAGE 64 V I DTTLRDG Q G+SL+VE+KV IA++L FG+ IE G+P ++ + E + G Sbjct: 2 VEILDTTLRDGTQGEGISLSVEDKVAIAKRLAAFGIHLIEGGWPGSNPKDAEFFARMKGV 61 Query: 65 ELDAEIC---------GLARCVKGDIDAAIDADVDCVHVFIATSDIHLRYKLEMSREEAL 115 +L GL + A ++A+ V +F + +H+ LE S EE L Sbjct: 62 DLGESRLAAFGATRRKGLLPEEDPSVLALLEAETPVVVLFGKSWTLHVLEALETSLEENL 121 Query: 116 ERAIEGVEYASDHGVTVEFSAE---DATRTDRDYLLEVYKATVEAGADRVNVPDTVGVMT 172 + V + + G V + AE D + D Y L +A ++ GAD + + DT G Sbjct: 122 RMVEDTVAFFASRGRRVIYDAEHFFDGYKEDPGYALATLEAALKGGADTLVLCDTNGGTL 181 Query: 173 PPEMYRLTAEVVDAVD-VPVSVHCHNDFGMAVANSLAAVEAGAEQVHVTVNGIGERAGNA 231 P E+Y +T VV+ V V +H HND +AVAN+LAAV AGA V T+NG GER GN Sbjct: 182 PEEVYAVTKVVVERFPGVRVGIHPHNDADLAVANALAAVRAGATHVQGTINGYGERCGNL 241 Query: 232 SLEQVVMALKALYDIEL--DVRTEMLVELSRLVERLTGVVVPPNTPIVGENAFAHESGIH 289 +L + L Y I R L ELS V+ + P VGE+AFAH++G+H Sbjct: 242 NLTSFLPNLVFKYHIPAIPPERLRGLKELSHFVDERANLTPNRRAPYVGESAFAHKAGVH 301 Query: 290 SHGVIKKAETYEPIRPEDVGHRRRIVLGKHAGRHAIKKKLEEMGIEVTEEQLDEIVRRVK 349 V+K TYE I PE VG+ RR ++ +GR + KL+E+G+++++E+ ++ VK Sbjct: 302 VSAVLKNPRTYEHIPPEWVGNGRRFLVSDVSGRSNLLAKLQELGVDLSKEEAKRLLDEVK 361 Query: 350 ELGDKGKRVTEDDLEAIARDVVGEVPESEAAVKLEEIAVMTGNKFTPT----ASVRVYLD 405 L +G + EA + + ++E +V T A+VRV + Sbjct: 362 ALEYEG--YAFEGAEASFYVLAHRLKGGSLPFQVEGFSVFVHGAGLATAWAEATVRVRVG 419 Query: 406 GE-EHEAASTGVGSVDAAIRALREAI----EELGMDVELKEYRLEAITG---GTDALAEV 457 EH AA + G V A RA R+A+ EL DVEL +Y++ ++G GT++ V Sbjct: 420 KTLEHTAAESPYGPVSALDRAFRKAVLGFYPELA-DVELADYKVRILSGREAGTNSGVRV 478 Query: 458 TVRLEDEDGNVTTARGAAEDIVMASVKAFVRG 489 V ++ G + GA+E+I+ AS+KA G Sbjct: 479 MVEMK-RGGERFSTVGASENILEASLKALTDG 509 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: 590 Number of extensions: 27 Number of successful extensions: 4 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: 526 Length adjustment: 35 Effective length of query: 464 Effective length of database: 491 Effective search space: 227824 Effective search space used: 227824 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