Align glutamyl-tRNAGlx synthetase (EC 6.1.1.17; EC 6.1.1.24) (characterized)
to candidate WP_077244519.1 B1A74_RS09765 glutamate--tRNA ligase
Query= metacyc::MONOMER-13959 (483 letters) >NCBI__GCF_001995255.1:WP_077244519.1 Length = 480 Score = 309 bits (791), Expect = 2e-88 Identities = 186/478 (38%), Positives = 269/478 (56%), Gaps = 20/478 (4%) Query: 6 RVRYAPSPTGHLHIGNARTALFNYLFARNQGGKFIIRVEDTDKKRNIEGGEQSQLNYLKW 65 R R+APSPTG LH+GN RTALF+ L AR +GG F++R+EDTD +R+ ++ L+W Sbjct: 10 RTRFAPSPTGLLHLGNLRTALFSALLARARGGHFLLRIEDTDAERSRAEFVEALQQDLQW 69 Query: 66 LGIDWDESVDVG-GEYGPYRQSERNDIYKVYYEELLEKGLAYKCYCTEEELEKEREEQIA 124 LG++WDE G+ GPY QS+R +Y+ YY+ L+ GLAY C+CT EELE+ R+ A Sbjct: 70 LGLNWDEGYGAAAGDAGPYAQSQRTGLYQAYYDRLIAAGLAYPCFCTPEELERGRKRMRA 129 Query: 125 RGEMPRYSGKHRDLTQEEQEKFIAEGRKPSIRFRVPEGKVIAFNDIVKGEISFESDGIGD 184 +G+ PRY G L EE + AEG++P++RFRVP G+ + F D V+G + F +D IGD Sbjct: 130 QGKPPRYPGTCAGLDPEEARRREAEGQRPTLRFRVPLGRTVRFEDGVRGAVKFRTDEIGD 189 Query: 185 FVIVKKDGTPTYNFAVAIDDYLMKMTHVLRGEDHISNTPKQIMIYQAFGWDIPQFGHMTL 244 FVI + DGTP + F+ A+DD LM +T V+RGEDHI+NTP+Q+++ +A P + H+ L Sbjct: 190 FVIRRSDGTPAFFFSNAVDDALMGVTDVVRGEDHIANTPRQLLLLEALELPAPGYHHLPL 249 Query: 245 IVNESRKKLSKRDESIIQFIEQYKELGYLPEALFNFIGLLGWSPVGEEELFTKEQFIEIF 304 + + LSKR+ S I + +E G LP A+ N + LG EE L + E + F Sbjct: 250 VNGDDGAPLSKRNGS--ASIRELREAGVLPLAILNHLARLG-HRYEEEGLLSLEGLAQGF 306 Query: 305 DVNRLSKSPALFDMHKLKWVNNQYVKKL-DLDQVVELTLPHLQKAGKVGTELSAEEQEWV 363 D R+ S A D +L+ + ++ L D D HL G + A W Sbjct: 307 DQGRIGHSAARHDPRQLEHWQAEALRALSDTD-----LQAHLAGLGVLDPLPEATRAAW- 360 Query: 364 RKLISLYHEQLSYGAEIVELTDLFFTDEIEYNQEAKAVLEEEQVPEVLSTFAAKLEELEE 423 I+L + ++ + F D + A+ +E + F A LE L+ Sbjct: 361 ---IALARDNIASVEDARCWVAAFAEDPAPLSDAAR----DEIAGAGPALFEAALEALD- 412 Query: 424 FTPDNIKASIKAVQKETGHKGKKLFMPIRVAVTGQTHGPELPQSIELIGKETAIQRLK 481 T + KA TG KG+ LFMP+R A++GQT GPELP+ E +G E RL+ Sbjct: 413 -TSTDFPEVAKAAGAATGRKGRGLFMPLRAALSGQTFGPELPRIREYLGPERTRVRLQ 469 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: 521 Number of extensions: 16 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: 483 Length of database: 480 Length adjustment: 34 Effective length of query: 449 Effective length of database: 446 Effective search space: 200254 Effective search space used: 200254 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