Align Glutamate--tRNA ligase; Glutamyl-tRNA synthetase; GluRS; EC 6.1.1.17 (characterized)
to candidate WP_066551960.1 A4249_RS08525 glutamate--tRNA ligase
Query= SwissProt::Q8DLI5 (485 letters) >NCBI__GCF_001636925.1:WP_066551960.1 Length = 444 Score = 276 bits (706), Expect = 1e-78 Identities = 184/471 (39%), Positives = 251/471 (53%), Gaps = 58/471 (12%) Query: 1 MTVRVRLAPSPTGNLHIGTARTAVFNWLYARHRGGKFILRIEDTDRERSRPEYTENILEG 60 M+V+VR APSPTG LH+G RTA+ NW++A+ +GG F+LRI+DTD RS PE+ + I + Sbjct: 1 MSVKVRFAPSPTGKLHVGNVRTALVNWMFAKGQGGSFVLRIDDTDLARSTPEFEQGIEDD 60 Query: 61 LQWLGLTWDEGPYFQSDRLDLYRQAIQTLLDKGLAYYCYCTPEELEALRAEQKAKGQAPR 120 L WLG+ WDE Y QS R D Y +A +L G Y Y T +EL+ R Q ++G P Sbjct: 61 LTWLGMPWDER-YNQSKRFDRYEEAAASLKASGRLYPAYETADELDRRRKVQLSRGLPPI 119 Query: 121 YDNRHRHLTPEEQAAFEAAGRTPVIRFKIEDDRQIEWQDLVRGRVSWQGADLGGDMVIAR 180 YD LT E++AA+EA GR P RFK+ D +++ W+DL RG A + ++I Sbjct: 120 YDRAALELTEEQKAAYEAEGRRPHWRFKL-DGKRVAWEDLARGHAEVDTASMSDPVLIR- 177 Query: 181 AAPRGEIGYPLYNLVVVVDDIAMGITDVIRGEDHIGNTPKQILLYEALGATPPNFAHTPL 240 E G LY L V+DDI MGIT +IRGEDH+ NT QI ++EALGAT P FAH PL Sbjct: 178 -----EDGLFLYTLPSVIDDIDMGITHIIRGEDHVTNTGAQIEIFEALGATVPGFAHMPL 232 Query: 241 ILNSTGQKLSKRDGVTSISDFRAMGYLAPALANYMTLLGWSPPEGVGELFTLDLAAKHFS 300 ++ + G LSKR G SISD R GY A+ +++ +G S P VG +++ + F+ Sbjct: 233 LVGADGAALSKRLGSLSISDMRDQGYEPIAITSHLGRIGTSDPLEVGA--SVEALGQSFA 290 Query: 301 FERINKAGARFDWDKLNWLNRQYIQQLEPEEFLAELIPLWQGAGYAFDEERDRPWLFDLA 360 F ++ ++ AR+D L+ LN Q + ++ E L L G AF W Sbjct: 291 FSKMGRSPARYDTADLDRLNAQALHVMDYETAQPRLQALGADLGEAF-------W----- 338 Query: 361 QLLQPGLNTLREAIDQGAVFFIPSVTFDSEAMAQLG----QP--QSATILAYLLEHLP-- 412 NT+R + + A D MAQ+ QP + AT + L LP Sbjct: 339 -------NTVRGNLTKFA---------DVADMAQIVRGPIQPVIEDATFIETALRLLPEV 382 Query: 413 ----AEPALTVAMGQQLIQQAAKAAGVKKGATMRTLRAALTGAVHGPDLMA 459 A A T A+ + G K A LR ALTG HGPD+ A Sbjct: 383 IDENAWSAWTSAVKAE--------TGAKGKALFMPLRLALTGQQHGPDMAA 425 Lambda K H 0.320 0.136 0.418 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: 593 Number of extensions: 24 Number of successful extensions: 6 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: 485 Length of database: 444 Length adjustment: 33 Effective length of query: 452 Effective length of database: 411 Effective search space: 185772 Effective search space used: 185772 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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