Align glutamate-tRNAGln ligase (EC 6.1.1.24) (characterized)
to candidate WP_086510764.1 BZY95_RS15280 glutamate--tRNA ligase
Query= BRENDA::Q9X2I8 (487 letters) >NCBI__GCF_002151265.1:WP_086510764.1 Length = 493 Score = 313 bits (803), Expect = 7e-90 Identities = 183/482 (37%), Positives = 279/482 (57%), Gaps = 32/482 (6%) Query: 25 VRVRFAPSPTGHLHVGGARTALFNWMFARKEGGKFILRIEDTDTERSSREYEQQILESLR 84 VR R APSPTG HVG A ALFN FAR+ GG+FILRIEDTD RS+ E E+ IL+SLR Sbjct: 3 VRTRIAPSPTGDPHVGTAYIALFNLCFARQHGGQFILRIEDTDRVRSTLESERMILDSLR 62 Query: 85 WCGLDWDEGPDIGGDFGPYRQSERLEIYREYAEKLVEDKRAY--YVVYDKEDPSKE---- 138 W GL+WDEGPD+GG GPYRQSER +IY EYA +L+E A+ Y ++ D +E Sbjct: 63 WLGLEWDEGPDVGGPHGPYRQSERGDIYAEYARQLIEAGHAFKCYRTSEELDELREARKA 122 Query: 139 -----------LFTTYEYPHEYKEKGHPVTIKFKV-LPGKTSFEDLLKGYMEFDNSTLED 186 L + + +G P ++ KV G +D+L+G +E D + ++ Sbjct: 123 SGMHLALKPDDLALPDDEVARREREGWPYVVRMKVPSSGTCVIDDMLRGTIEVDWAQVDA 182 Query: 187 FIIMKSNGFPTYNFAVVVDDHLMRISHVFRGEDHLSNTPKQLMIYEAFGWEAPVFMHIPL 246 +++KS+G PTY+ A VVDDHLM I+HV RGE+ +++ PK ++YE FGWE PV H+PL Sbjct: 183 QVLLKSDGMPTYHLANVVDDHLMGITHVLRGEEWINSAPKHQLLYEYFGWEMPVLCHMPL 242 Query: 247 ILGSDRTPLSKRHGATSVEHFRREGILSRALMNYLALLGWRVEGD-EIFTIEEKLQSFDP 305 + D++ LSKR TS+ +++R G L +A++NYL +GW + + E F+++E + FD Sbjct: 243 LRNPDKSKLSKRKNPTSINYYKRMGFLPQAVINYLGRMGWSMPDEREKFSLDEMMAHFDI 302 Query: 306 KDISNKGVIFDYQKLEWVNGKHMRRIDLED--LKREFIEWAKYAGKEIPSVDERYFSETL 363 + +S G +FD +KL W+NG ++R DL+D + +EWA +E Y + L Sbjct: 303 QRVSLGGPVFDLEKLTWLNGLYIRE-DLDDRAFLKALMEWA---------FNEEYVGQIL 352 Query: 364 RICREKVNTLSQLYDIMYPFMNDDYEY-EKDYVEKFLKREEAERVLEEAKKAFKDLNSWN 422 R +V TLSQ+ + F + + E+D+ L+REE R+L+ F+ + +W+ Sbjct: 353 PQVRTRVETLSQVAPLAGHFFSGVPDVREQDFDGIKLEREELVRLLQFLVWRFEAVPAWH 412 Query: 423 MEEIEKTLRDLSEKGLASKKVVFQLIRGAVTGKLVTPGLFETIEVLGKERTLKRLERTLQ 482 E + ++ L+ K + A+TG + + + + +LG + T RL ++ Sbjct: 413 KEALLAEVKLLAGHFGFKMKDFLAPVFIAITGSAASTSVMDAMAILGSDVTRARLRHAIE 472 Query: 483 FL 484 L Sbjct: 473 VL 474 Lambda K H 0.320 0.139 0.416 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: 703 Number of extensions: 46 Number of successful extensions: 5 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: 487 Length of database: 493 Length adjustment: 34 Effective length of query: 453 Effective length of database: 459 Effective search space: 207927 Effective search space used: 207927 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: 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