Align Probable 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate WP_020175256.1 A3OQ_RS0110050 citramalate synthase
Query= curated2:Q8TYB1 (499 letters) >NCBI__GCF_000385335.1:WP_020175256.1 Length = 531 Score = 228 bits (581), Expect = 4e-64 Identities = 173/519 (33%), Positives = 270/519 (52%), Gaps = 32/519 (6%) Query: 3 DRVRIFDTTLRDGEQTPGVSLTVEEKVEIARKLDEFGVDTIEAGFPVASEGE--FEAVRA 60 + + +FDTTLRDG QT GV ++++K IA LD+ G+D IE G+P A+ + F A R Sbjct: 4 ETLALFDTTLRDGAQTTGVDFSLDDKRHIAALLDDLGLDYIEGGYPGANPTDTAFFAKRP 63 Query: 61 IAGEELDAEICGLA----RCVKGD--IDAAIDADVDCVHVFIATSDIHLRYKLEMSREEA 114 + + A G+ R V D + + +AD D + T D +R L + +E Sbjct: 64 VLKKARFAAF-GMTKRAGRSVANDPGLASLFEADADVITYVAKTWDYQVRVALGCTLDEN 122 Query: 115 LERAIEGVEYASDHGVTVEFSAE---DATRTDRDYLLEVYKATVEAGADRVNVPDTVGVM 171 LE + VE A+ G V E D + + Y L+ KA AGA + + DT G Sbjct: 123 LEGISQSVEAAAARGREVILDCEHFFDGYKANPAYALDCAKAAHAAGARWIVLCDTNGGS 182 Query: 172 TPPEMYRLTAEVVDAVDVP-VSVHCHNDFGMAVANSLAAVEAGAEQVHVTVNGIGERAGN 230 P E+ R+ EV + + +H HND AVANSLAAV AGA + T+NG+GER GN Sbjct: 183 LPHEVERIVTEVTAHIPGSHLGIHAHNDTEHAVANSLAAVRAGARHIQGTLNGLGERCGN 242 Query: 231 ASLEQVVMALKALYDI----ELDVRTEMLVELSRLVERLTGVVV-PPN--TPIVGENAFA 283 A+L ++ L D E+ V E L +++++ L ++ PN P VG +AFA Sbjct: 243 ANLMSIIPTLLLKKDYADHYEIGVPLEKLAQITKISHALDELLNRQPNRHAPYVGASAFA 302 Query: 284 HESGIHSHGVIKKAETYEPIRPEDVGHRRRIVLGKHAGRHAIKKKLEEMGIEVTEE--QL 341 ++GIH+ V+K TYE + PE VG++R++++ AGR I +LE +G+ + ++ ++ Sbjct: 303 TKAGIHASAVLKDPATYEHVTPESVGNQRKVIVSDQAGRSNILAELERIGVMLAKDDPRI 362 Query: 342 DEIVRRVKELGDKGKRV--TEDDLEAIARDVVGEVPE----SEAAVKLEEIAVMTGNKFT 395 + ++ VKE G E E + R V+GEVP+ +V +E G+ T Sbjct: 363 NRLLDEVKEKESLGYAYEGAEASFELLVRRVLGEVPDYFDVERFSVGVERRHNAQGDLVT 422 Query: 396 PT-ASVRVYLDGEEHEAASTGVGSVDAAIRALREAI---EELGMDVELKEYRLEAITGGT 451 + A V+V + E +A+ G+G V+A ALR+ + + DVEL +YR+ GGT Sbjct: 423 VSEAVVKVRVHDELLLSAAEGIGPVNALDLALRKDLGRYQRFIEDVELVDYRVRVFQGGT 482 Query: 452 DALAEVTVRLEDEDGNVTTARGAAEDIVMASVKAFVRGV 490 DA+ V V D+D + G + +I+ AS +A + Sbjct: 483 DAVTRVLVEFADKDDMRWSTVGVSANIIDASFQALTDAI 521 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: 540 Number of extensions: 23 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: 531 Length adjustment: 35 Effective length of query: 464 Effective length of database: 496 Effective search space: 230144 Effective search space used: 230144 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