Align Probable 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate WP_034273566.1 AMYHA_RS20250 citramalate synthase
Query= curated2:Q8TYB1 (499 letters) >NCBI__GCF_000504245.1:WP_034273566.1 Length = 544 Score = 202 bits (515), Expect = 2e-56 Identities = 172/518 (33%), Positives = 257/518 (49%), Gaps = 41/518 (7%) Query: 3 DRVRIFDTTLRDGEQTPGVSLTVEEKVEIARKLDEFGVDTIEAGFPVA--SEGEFEAVRA 60 D ++DTTLRDG Q G+S +V +K+ +AR LDE GV IE G+P A + EF A RA Sbjct: 13 DTFHVYDTTLRDGAQREGISYSVTDKLAVARLLDELGVGFIEGGWPGALPKDTEFFA-RA 71 Query: 61 IAGEEL--DAEICGLARCVKGDIDAAIDADVDC-------VHVFIATSDI-HLRYKLEMS 110 +GE A + K A+ DA V V +A SD H+ L++ Sbjct: 72 SSGELALKHAALVAFGATRKAGTTASEDAQVRALLDSNAPVITLVAKSDRRHIERALKVD 131 Query: 111 REEALERAIEGVEYASDHGVTVEFSAE---DATRTDRDYLLEVYKATVEAGADRVNVPDT 167 EA + V + G V AE D D D L V +A + GAD + DT Sbjct: 132 VAEACAMVRDTVSFLVSEGRRVFLDAEHFFDGYAFDPDTALRVLRAGADGGADVAVLCDT 191 Query: 168 VGVMTPPEMYRLTAEVVDAVDVPVSVHCHNDFGMAVANSLAAVEAGAEQVHVTVNGIGER 227 G P + EV D + + +HC +D AVANS+AAV+AGA V T NG GER Sbjct: 192 NGGQLPLGIAETVREVADKTGLRLGIHCQDDTSCAVANSVAAVQAGATHVQCTANGYGER 251 Query: 228 AGNASLEQVVMALKALYDIELDVRTEMLVELSRLVERLTGVV-VPPNT--PIVGENAFAH 284 AGNA L V+ L D+++ + T EL+R+ L + + P+T VG +AFAH Sbjct: 252 AGNADLFAVIGNLVTKLDMDV-LPTGGAAELTRVSHALAEIANIAPDTHQAYVGASAFAH 310 Query: 285 ESGIHSHGVIKKAETYEPIRPEDVGHRRRIVLGKHAGRHAIKKKLEEMGIEVTEE--QLD 342 ++G+H+ + Y I P VG+ R+++ + AGR +++ K E+G+++ + L Sbjct: 311 KAGLHASAIKVDPLLYNHIDPPVVGNDMRVLVTEMAGRASLELKGRELGVDLASQPTALT 370 Query: 343 EIVRRVKELGDKG--KRVTEDDLEAIAR-------DVVGEVPESEAAVKLEEIAVM---- 389 +V +VK L KG + LE + R D G+ EA +LE V+ Sbjct: 371 NVVEKVKALEAKGWSFEAADASLELLLRRAMDDDGDGSGDTLAPEAPFELESYRVVLDHR 430 Query: 390 TGNKFTPTASVRVYLDGEEHEAASTGVGSVDAAIRALREAIEE--LGMD-VELKEYRLEA 446 + ++ A+V+V++ GE A + G G V A ALR+A+ +D V+L +Y++ Sbjct: 431 SNDEVISEATVKVHVAGERVIATAEGNGPVHALDAALRKALTPRLAWLDSVDLTDYKVRI 490 Query: 447 ITG--GTDALAEVTVRLEDEDGNVTTARGAAEDIVMAS 482 + G GT+A+ V + D + TT G E+IV AS Sbjct: 491 LPGTHGTEAVTRVLIESSDREREWTTV-GVHENIVEAS 527 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: 584 Number of extensions: 25 Number of successful extensions: 3 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: 544 Length adjustment: 35 Effective length of query: 464 Effective length of database: 509 Effective search space: 236176 Effective search space used: 236176 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 26 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