Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_084276501.1 B8779_RS09685 2-isopropylmalate synthase
Query= curated2:Q8TYM1 (509 letters) >NCBI__GCF_900176045.1:WP_084276501.1 Length = 516 Score = 382 bits (982), Expect = e-110 Identities = 208/509 (40%), Positives = 320/509 (62%), Gaps = 21/509 (4%) Query: 12 DEVRIFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIA 71 ++V+IFDTTLRDGEQ+PG ++ EEK++IA++L+++GVD IEAGFAAAS G+ +AIR+I+ Sbjct: 3 EQVKIFDTTLRDGEQSPGASMNTEEKIQIAKQLEKLGVDIIEAGFAAASPGDFEAIRKIS 62 Query: 72 REELDAEVCSMARMVKGDVDAAVEAEADA----VHIVVPTSEVHVKKKLRMDREEVLERA 127 + VCS+AR ++ D+ AA EA A A +H + TS +H+K KLRM+ EEV++RA Sbjct: 63 EVVNKSTVCSLARALEKDIKAAGEAIAPAKFKRIHTFIATSPIHMKYKLRMEPEEVIKRA 122 Query: 128 REVVEYARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFL 187 E V+YA+ VE S ED R+E+ +L E+ A +EAGA+ + DTVG P M Sbjct: 123 IEAVKYAKTFVNDVEFSCEDAGRSEMAFLKEIIAAVIEAGAKTINIPDTVGYRFPHEMGE 182 Query: 188 AVKKLRERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEV 247 +K+L++ +GE I+SVHCH+D G+A AN++ +V GARQV T+NG+GERAGNAALEE+ Sbjct: 183 MIKELKDFIGERAIISVHCHNDLGLAVANSLYSVLNGARQVECTINGLGERAGNAALEEI 242 Query: 248 VVVLEE----LYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADG 303 V+ ++ G+DT I T+ + S+LV +TG+ PNKA+VG+NAF HESGIH DG Sbjct: 243 VMAIKTRKDIFDGIDTNINTKEIYPTSRLVAAITGIEPQPNKAIVGKNAFAHESGIHQDG 302 Query: 304 ILKDESTYEPIPPEKVGHERR-FVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRL 362 +LK + TYE + E +G +R VLGKH G +K+++ +G + +E++ + R K L Sbjct: 303 VLKHQETYEIMRAEDIGLDRNAIVLGKHSGRHAFKKRIEDLGFTLSEEEINKAFERFKVL 362 Query: 363 GDRGKRITEADLRAIAEDVLGRPAE----RDIEVEDFTTVTGKRTIPTASIVVKIDGTRK 418 D+ K IT+ D+R + + + E + +++ D + +P+A++ ++ DG Sbjct: 363 ADKKKEITDDDIRMLITNEIASAPEVYKLKKLQISDCS-----EGVPSAAVTIEFDGKEI 417 Query: 419 EAASTGVGPVDATIKALERALKDQGIDFELVEYRAEALTGGTDAITHVDVKLRDPETGDI 478 A G G +DA K ++R G L +Y+ A++ G DA+ V VK+ E Sbjct: 418 TDAGIGDGTIDAIFKTIDRI---SGYKGTLNDYQVAAVSKGKDALAKVVVKVVFDEKKPA 474 Query: 479 VHSGSSREDIVVASLEAFIDGINSLMARK 507 V D ++AS +A++ +NS ++ K Sbjct: 475 VIGHGLSIDTMIASAKAYVSALNSYISMK 503 Lambda K H 0.315 0.134 0.367 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: 657 Number of extensions: 39 Number of successful extensions: 7 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: 509 Length of database: 516 Length adjustment: 35 Effective length of query: 474 Effective length of database: 481 Effective search space: 227994 Effective search space used: 227994 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 (21.6 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