Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_017548412.1 C792_RS0105305 2-isopropylmalate synthase
Query= curated2:O26819 (496 letters) >NCBI__GCF_000330705.1:WP_017548412.1 Length = 515 Score = 360 bits (924), Expect = e-104 Identities = 209/507 (41%), Positives = 303/507 (59%), Gaps = 29/507 (5%) Query: 2 QVRVLDTTLRDGEQTPGVSLTPEEKLRIALKIDALGADIIEAGSAITSEGEREGIRKITS 61 ++R+ DTTLRDGEQ+PGV+L EKL IA +++ LG D++EAG SEG+ + +R I Sbjct: 3 RIRIFDTTLRDGEQSPGVNLNKMEKLEIAKQLEKLGVDVMEAGFPAASEGDFQAVRLIAD 62 Query: 62 EGLRAEICSFARAVREDIDAAISCDVDS----VHLVVPTSDLHLEHKLRKTREEVLEQAV 117 + + AR +EDID A ++ +H+ + TS +H+E+KL+ T EEV++Q+V Sbjct: 63 TVTDVSVTALARTRKEDIDRAWEALKNTPNPRIHIFLATSPIHMEYKLKMTPEEVIKQSV 122 Query: 118 DCTEYAVDHGILVELSAEDSTRSDMDFLRTIFREGIEAGAERICACDTVGILTPERSYEF 177 D YA + VE SAED+TRSD DF+ I + I+ GA I DTVG TP+ Sbjct: 123 DMVRYARERFSEVEWSAEDATRSDWDFMANIIEQVIDVGATVINLPDTVGYTTPDEYGRM 182 Query: 178 YRGLSE-----LGAPLSVHCHNDFGLAVANSLAGLRAGASEVHATINGIGERAGNAALEE 232 ++ + E A LS HCHND GLA AN++A + GA++V TINGIGERAGN ALEE Sbjct: 183 FKYMKENVPNIAKADLSCHCHNDLGLAAANTMAAIENGATQVEGTINGIGERAGNVALEE 242 Query: 233 VVVALK---SLYDVDTSINIEMLYETSRMVARMTGVYLQPNKAIVGENAFAHESGIHADG 289 V VAL Y+ +T + ++ + TS ++A+++G+Y+Q NKAI+G NA+AHESGIH DG Sbjct: 243 VAVALHIRADRYNYETGLKLDEIKRTSDLIAKLSGMYVQANKAIIGRNAYAHESGIHQDG 302 Query: 290 VLKKAETYEPITPEMVG-HGRGFVMGKHIGTHALRKRLDELGMKVADDKLMEIFRRVKTL 348 VLK AETYE ITPE+VG MGKH G HA + ++ E G+++ D+++ FRR K L Sbjct: 303 VLKNAETYEIITPELVGVSSNTLFMGKHSGKHAFKDKVKEFGVEMTDEEVKSTFRRFKEL 362 Query: 349 GDMGKCVTDVDLQAIAEDVLGVMEDKVV-------DLQEVTIVSGNRVTPTASVKLRVD- 400 D + VTD D+ + +ME K L+ + G TA+V L Sbjct: 363 TDHKREVTDDDIYTL------IMETKTAHSAVNKYSLENFQVNYGTANITTATVSLSTPA 416 Query: 401 DREVLEAGTGVGPVDAAIVAIKKSLEDFADITLEEYHVDAITGGTDALIDVVIKLRHGDR 460 R V A TG G V+A I++ ++ A++ L +Y ++++ GG DAL + ++L Sbjct: 417 GRTVQTAATGNGSVEALYKTIQELID--AELKLLDYQLNSVGGGKDALAESHVQLLVNGE 474 Query: 461 IISARSTQPDIIMASVEAFLSGVNRLL 487 + R T D+I AS A+++ VNR L Sbjct: 475 RTNGRGTAQDVIEASANAYINAVNRYL 501 Lambda K H 0.317 0.135 0.373 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: 601 Number of extensions: 27 Number of successful extensions: 6 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: 496 Length of database: 515 Length adjustment: 34 Effective length of query: 462 Effective length of database: 481 Effective search space: 222222 Effective search space used: 222222 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 (21.7 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