Align glutamyl-tRNAGlx synthetase (EC 6.1.1.17; EC 6.1.1.24) (characterized)
to candidate WP_012675348.1 PERMA_RS09495 glutamate--tRNA ligase
Query= metacyc::MONOMER-13959 (483 letters) >NCBI__GCF_000021565.1:WP_012675348.1 Length = 478 Score = 462 bits (1190), Expect = e-135 Identities = 222/478 (46%), Positives = 327/478 (68%), Gaps = 9/478 (1%) Query: 5 VRVRYAPSPTGHLHIGNARTALFNYLFARNQGGKFIIRVEDTDKKRNIEGGEQSQLNYLK 64 VRVR+APSPTG+LH+GNARTALFNY++AR+ GGK I+R+EDTD++R+ + E ++ LK Sbjct: 2 VRVRFAPSPTGYLHLGNARTALFNYIYARHTGGKLILRIEDTDRERSKKEYEDLLIDDLK 61 Query: 65 WLGIDWDESVDVGGEYGPYRQSERNDIYKVYYEELLEKGLAYKCYCTEEELEKEREEQIA 124 WLGI+WDE D+GG+YGPYRQSER DIY Y E+L E G YKC+C+ EELE+ER++ ++ Sbjct: 62 WLGIEWDEGPDIGGDYGPYRQSERTDIYNQYVEKLKESGHIYKCFCSPEELEEERKKALS 121 Query: 125 RGEMPRYSGKHRDLTQEEQEKFIAEGRKPSIRFRVPEGKVIAFNDIVKGEISFESDGIGD 184 G PRYSGK R+LT+++ +K +EG+ RFRVP+G+ I F D++KG + D GD Sbjct: 122 EGRPPRYSGKCRNLTEDQIKKLESEGKPYVWRFRVPDGEFIIFEDVIKGTVEINVDEFGD 181 Query: 185 FVIVKKDGTPTYNFAVAIDDYLMKMTHVLRGEDHISNTPKQIMIYQAFGWDIPQFGHMTL 244 FVIV+ DG+P YNF V +DD LMK+T V+RGEDH+SNTPKQI+IY+A G++ P+F H+ + Sbjct: 182 FVIVRSDGSPVYNFVVVVDDALMKITDVIRGEDHLSNTPKQILIYRALGFEEPRFAHLPI 241 Query: 245 IVNESRKKLSKRDESIIQFIEQYKELGYLPEALFNFIGLLGWSPVGEEELFTKEQFIEIF 304 I+ E R KLSKR ++ + +++ GY+ EA+FN + LLGW P G+ E+ +KE+ I F Sbjct: 242 ILGEDRSKLSKRHGAV--SVRAFRDDGYVSEAMFNGLSLLGWHPKGDNEVLSKEEIIREF 299 Query: 305 DVNRLSKSPALFDMHKLKWVNNQYVK-KLDLDQVVELTLPHLQKAGKVGTELSAEEQEWV 363 D+ + +PA+FD KL+W+N Y++ K+DLD + E +P + G + ++ Sbjct: 300 DIKDIHNAPAVFDRAKLRWLNGVYIREKIDLDDLTERAVPFFEGFG------YKADFDYY 353 Query: 364 RKLISLYHEQLSYGAEIVELTDLFFTDEIEYNQEAKAVLEEEQVPEVLSTFAAKLEELEE 423 RK++ + L +I + FF D+ Y ++A+ L++E V+ F K+++++E Sbjct: 354 RKVMEAIRDSLETLMDIEQRAKPFFVDDFHYEEDAQQFLKDETGYRVVQLFYEKVKDMDE 413 Query: 424 FTPDNIKASIKAVQKETGHKGKKLFMPIRVAVTGQTHGPELPQSIELIGKETAIQRLK 481 ++ K K +QKE G KGK LFMPIRVA+TG T G ++ +E+IG E RL+ Sbjct: 414 IKKEDFKRITKEIQKELGVKGKNLFMPIRVALTGVTSGVDMAVLVEVIGVERVKHRLQ 471 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: 684 Number of extensions: 29 Number of successful extensions: 4 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: 478 Length adjustment: 34 Effective length of query: 449 Effective length of database: 444 Effective search space: 199356 Effective search space used: 199356 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