Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_012992063.1 THAL_RS05225 2-isopropylmalate synthase
Query= curated2:Q8TYM1 (509 letters) >NCBI__GCF_000025605.1:WP_012992063.1 Length = 519 Score = 412 bits (1058), Expect = e-119 Identities = 227/509 (44%), Positives = 334/509 (65%), Gaps = 19/509 (3%) Query: 12 DEVRIFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIA 71 ++V IFDTTLRDGEQ PG ++T EEKL++A +L +GVD +EAGFAAAS+G+ +A++ IA Sbjct: 2 EKVYIFDTTLRDGEQAPGFSMTSEEKLQMALQLARLGVDVLEAGFAAASKGDYEAVKLIA 61 Query: 72 REELDAEVCSMARMVKGDVDAAVEAEADA----VHIVVPTSEVHVKKKLRMDREEVLERA 127 +E +CS+AR ++ D+D A EA A A +H + TSE+H++ KLRM ++VLERA Sbjct: 62 QEVKGPVICSLARALEKDIDLAAEALAPAERKRIHTFIATSEIHMRYKLRMSPQDVLERA 121 Query: 128 REVVEYARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFL 187 + V YAR + VE S ED TR++ E+LY V + ++AGA + DTVG PE Sbjct: 122 KRAVSYARRYTDDVEFSCEDATRSQREFLYRVIEEAIKAGATVINIPDTVGYSVPEEFAQ 181 Query: 188 AVKKLRERVG--EDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALE 245 ++ +R V + VI+SVHCHDD G+A AN++ AV+ GARQV T+NGIGERAGNAALE Sbjct: 182 LIEDIRNNVPNIDKVIISVHCHDDLGLAVANSLMAVKHGARQVECTINGIGERAGNAALE 241 Query: 246 EVVVVL---EELYG-VDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHA 301 EVV+ L ++ +G + T I T+ + + S+L+ R+TG V PNKA+VG+NAF+HESGIH Sbjct: 242 EVVMALKVRKDFFGDLYTSINTKEIYKTSRLLCRITGSFVQPNKAIVGDNAFSHESGIHQ 301 Query: 302 DGILKDESTYEPIPPEKVGH-ERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLK 360 G+L + TYE + PE VG R +LGKH G ++KKL+QMG++V + +L I + K Sbjct: 302 HGVLSNPLTYEIMNPEDVGFPSSRIILGKHSGRHALKKKLQQMGIEVSEAELERIFEKFK 361 Query: 361 RLGDRGKRITEADLRAIA-EDVLGRPAERDIEVEDFTTVTGKRTIPTASIVVKIDGTRKE 419 L D+ K I + DL A+ E+V+ P ++ + V + TG + +PTA++V++ G + Sbjct: 362 ELADKKKEIYDEDLEALVYEEVMKLPDDQPVSVLHYQVQTGDKLLPTATVVIRYMGQERT 421 Query: 420 AASTGVGPVDATIKALERALKDQGIDFELVEYRAEALTGGTDAITHVDVKLRDPETGDIV 479 A +TG GPVDA IKA+++AL +D +L+++ +ALT TDA + + E + Sbjct: 422 ATATGNGPVDAVIKAIQKAL---DLDTKLLDFSIKALTPNTDAQAEARLVI---ELDGVR 475 Query: 480 HSGSSRE-DIVVASLEAFIDGINSLMARK 507 SG + DI+ AS+ F+D +N + RK Sbjct: 476 SSGRGVDVDIIKASVVGFVDAVNRALLRK 504 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: 644 Number of extensions: 27 Number of successful extensions: 9 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: 519 Length adjustment: 35 Effective length of query: 474 Effective length of database: 484 Effective search space: 229416 Effective search space used: 229416 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