Align glutamyl-tRNAGlx synthetase (EC 6.1.1.17; EC 6.1.1.24) (characterized)
to candidate GFF1264 Psest_1297 glutamyl-tRNA synthetase, bacterial family
Query= metacyc::MONOMER-13959 (483 letters) >FitnessBrowser__psRCH2:GFF1264 Length = 493 Score = 338 bits (867), Expect = 2e-97 Identities = 182/480 (37%), Positives = 277/480 (57%), Gaps = 16/480 (3%) Query: 5 VRVRYAPSPTGHLHIGNARTALFNYLFARNQGGKFIIRVEDTDKKRNIEGGEQSQLNYLK 64 VR R APSPTG H+G A ALFN FAR GG+FI+R+EDTD+ R+ EQ + L+ Sbjct: 4 VRTRIAPSPTGDPHVGTAYIALFNLCFARQHGGQFILRIEDTDQLRSTRESEQQIYDALR 63 Query: 65 WLGIDWDESVDVGGEYGPYRQSERNDIYKVYYEELLEKGLAYKCYCTEEELEKEREEQIA 124 WLGI+WDE DVGG +GPYRQSER +IYK Y +EL+ KG A+ C+C+ E L++ R EQ+A Sbjct: 64 WLGIEWDEGPDVGGPHGPYRQSERGEIYKKYSDELVAKGHAFPCFCSSERLDQVRAEQMA 123 Query: 125 RGEMPRYSGKHRDLTQEEQEKFIAEGRKPSIRFRVPEGKVIAFNDIVKGEISFESDGIGD 184 E PRY G L E ++ IA G IR +VP V D+++G + D + Sbjct: 124 NKETPRYDGHCMHLEPAEAQRRIAAGESHVIRMKVPSEGVCQVQDMLRGTVEIGWDRMDM 183 Query: 185 FVIVKKDGTPTYNFAVAIDDYLMKMTHVLRGEDHISNTPKQIMIYQAFGWDIPQFGHMTL 244 V++K DG PTY A +DD+LM +THVLRGE+ + + PK I +Y+ FGW+ PQ +M L Sbjct: 184 QVLMKADGLPTYFLANVVDDHLMGITHVLRGEEWLPSAPKLIKLYEYFGWEQPQLCYMPL 243 Query: 245 IVNESRKKLSKRDESIIQFIEQYKELGYLPEALFNFIGLLGWSPVGEEELFTKEQFIEIF 304 + N + KLSKR + Y+ +G+LP+A+ N++G +GWS E E FT ++ IE F Sbjct: 244 LRNPDKSKLSKRKNP--TSVTFYERMGFLPQAMLNYLGRMGWSMPDEREKFTLDEMIEHF 301 Query: 305 DVNRLSKSPALFDMHKLKWVNNQYVKKLDLDQVVELTLPHLQKAGKVGTELSAEEQEWVR 364 D+ R+S +FD+ KL W+N Q++++L ++Q +QK A +++ Sbjct: 302 DIQRVSLGGPIFDLEKLSWLNGQWLRELSVEQFA----TEVQK--------WAFNLQYMM 349 Query: 365 KLISLYHEQLSYGAEIVELTDLFFTDEIEYNQE--AKAVLEEEQVPEVLSTFAAKLEELE 422 ++ +++ ++I L FF+ + + A L+ QV +V+ KLE L Sbjct: 350 QIAPHVQQRVETFSQIAPLAGFFFSGALPLDPALFAHKKLDAAQVRQVMQLILWKLEALR 409 Query: 423 EFTPDNIKASIKAVQKETGHKGKKLFMPIRVAVTGQTHGPELPQSIELIGKETAIQRLKN 482 ++ + I A I V + G K + + + A+TGQ + ++E++G + RL+N Sbjct: 410 QWEKERITACITQVAEHLGFKLRDVMPLMFAAITGQASSVSVLDAMEILGPDLTRFRLRN 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: 606 Number of extensions: 30 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: 493 Length adjustment: 34 Effective length of query: 449 Effective length of database: 459 Effective search space: 206091 Effective search space used: 206091 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