Align glutamyl-tRNAGlx synthetase (EC 6.1.1.17; EC 6.1.1.24) (characterized)
to candidate WP_018234027.1 THITHI_RS0115525 glutamate--tRNA ligase
Query= metacyc::MONOMER-13959 (483 letters) >NCBI__GCF_000378965.1:WP_018234027.1 Length = 473 Score = 319 bits (818), Expect = 1e-91 Identities = 182/482 (37%), Positives = 273/482 (56%), Gaps = 29/482 (6%) Query: 5 VRVRYAPSPTGHLHIGNARTALFNYLFARNQGGKFIIRVEDTDKKRNIEGGEQSQLNYLK 64 V+ R+APSPTGHLH+GN RTALF+ L AR +GG F++R+EDTD R+ + + + L+ Sbjct: 6 VKTRFAPSPTGHLHLGNLRTALFSALLARREGGVFLLRIEDTDAARSSDAHVHALMEDLR 65 Query: 65 WLGIDWDESVDVGGEYGPYRQSERNDIYKVYYEELLEKGLAYKCYCTEEELEKEREEQIA 124 WLG++W E +VGG GPY QS R IY Y L GLAY C+C++E L R+ Q+A Sbjct: 66 WLGLEWQEGPEVGGPNGPYAQSLRGHIYAADYSRLESAGLAYPCFCSDEILRLSRKAQLA 125 Query: 125 RGEMPRYSGKHRDLTQEEQEKFIAEGRKPSIRFRVPEGKVIAFNDIVKGEISFESDGIGD 184 G+ PRY G L+ ++ + +G KP++RFRVP G+ I F+D+V+G F++D IGD Sbjct: 126 AGQPPRYPGTCARLSPQDVRARLDKGLKPTLRFRVPPGRRIRFDDLVRGSQVFDTDTIGD 185 Query: 185 FVIVKKDGTPTYNFAVAIDDYLMKMTHVLRGEDHISNTPKQIMIYQAFGWDIPQFGHMTL 244 FVI + DGTP++ F+ A+DD +M +THVLRGEDH++NTP+Q+M+ +A +P +GH++L Sbjct: 186 FVIRRSDGTPSFFFSNAVDDAMMGVTHVLRGEDHLANTPRQMMVMEALDLPVPAYGHISL 245 Query: 245 IVNESRKKLSKRDESIIQFIEQYKELGYLPEALFNFIGLLGWSPVGEEELFTKEQFIEI- 303 I+ E LSKR ++ + + ++ GYLP+AL N + LG S + + F+++ Sbjct: 246 ILGEDGAPLSKRHGALS--LRELRDRGYLPQALLNHLARLGHS-------YEADGFMDLD 296 Query: 304 -----FDVNRLSKSPALFDMHKLKWVNNQYVKKLDLDQVVELTLPHLQKAGKVGTELSAE 358 FD RL ++PA D +L +Q V L D + P L+ G Sbjct: 297 ALARGFDAARLGRAPARHDPVQLDHWQHQAVLALADDGLARWLGPMLEDEVPAGAR---- 352 Query: 359 EQEWVRKLISLYHEQLSYGAEIVELTDLFFTDEIEYNQEAKAVLEEEQVPEVLSTFAAKL 418 + + + +S+ E + F + EA V+ + F A L Sbjct: 353 -----GPFLRVVRDNISFPGEARDWARRLFGAPPVPDAEAGQVMARAGS----AFFDAAL 403 Query: 419 EELEEFTPDNIKASIKAVQKETGHKGKKLFMPIRVAVTGQTHGPELPQSIELIGKETAIQ 478 L +P + + V TG KG+ LFMP+R A+TG+THGPE+ L+G E + Sbjct: 404 VALAA-SPGDFRVLAGQVGTATGLKGRHLFMPLRAALTGRTHGPEMKDLWPLLGPERVAE 462 Query: 479 RL 480 RL Sbjct: 463 RL 464 Lambda K H 0.316 0.137 0.394 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: 530 Number of extensions: 20 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 483 Length of database: 473 Length adjustment: 34 Effective length of query: 449 Effective length of database: 439 Effective search space: 197111 Effective search space used: 197111 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: 51 (24.3 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