Align glutamyl-tRNA(Glx) synthetase (EC 6.1.1.24) (characterized)
to candidate WP_077278500.1 B1C78_RS07285 glutamate--tRNA ligase
Query= reanno::Caulo:CCNA_01982 (470 letters) >NCBI__GCF_002000365.1:WP_077278500.1 Length = 470 Score = 362 bits (930), Expect = e-104 Identities = 200/465 (43%), Positives = 279/465 (60%), Gaps = 14/465 (3%) Query: 9 VVTRFAPSPTGFLHIGGARTALFNWLYARHTGGKFLIRVEDTDRERSTEAAVAAIFEGLD 68 V TRFAPSPTG+LHIGGARTALF+WLYAR GG F++RVEDTD RS +V AI EG++ Sbjct: 3 VRTRFAPSPTGYLHIGGARTALFSWLYARKHGGDFVLRVEDTDLARSNAESVNAILEGMN 62 Query: 69 WLGLKSDDEVIFQHTRAPRHVEVVHELLAKGRAYRCWMSIEELEVAR-------EKARAE 121 WLGL+ D+ +Q R R+ EVV LL +G+AY C+ + EEL+ R +K R + Sbjct: 63 WLGLEYDEGPFYQTQRFERYREVVQRLLDEGKAYHCYCTKEELDAMRAEQMASKQKPRYD 122 Query: 122 GRAIRSPWRDAPEGDLSAPHVIRFKGPLDGETLVNDLVKGPVTFKNIELDDLVLLRADGA 181 GR R E V+RF+ DG T+V D+V+G V F+N ELDDL++ R+DG+ Sbjct: 123 GRC-----RHRTEPREGVEPVVRFRNADDGVTVVEDMVRGRVVFQNSELDDLIIARSDGS 177 Query: 182 PTYNLAVVVDDHDMGVTHVIRGDDHLNNAARQTLIYQAMDWAVPAFAHIPLIHGPDGAKL 241 PTYNL VVVDD DM +THVIRGDDHLNN RQ I +A+D P +AH+P+I GPDG KL Sbjct: 178 PTYNLTVVVDDWDMQITHVIRGDDHLNNTPRQINILKALDVEPPKYAHLPMILGPDGTKL 237 Query: 242 SKRHGAQAVGEFADLGYIPEGMRNYLARLGWGHGDDEVFTDEQAISWFDVADVVKAPARL 301 SKRHGA +V ++ D G++PE + NYL RLGW HGD EVFT E+ I FD+ DV + + + Sbjct: 238 SKRHGAVSVMQYRDDGFLPEALINYLVRLGWSHGDQEVFTLEELIELFDIVDVNHSASAI 297 Query: 302 DWAKLNHINAQHLRKADDARLTALALAAAETRGEPLPADAAERIARTVPEVKEGAKTILE 361 + KL +N +++ +D + G + A + V +E AKT+ E Sbjct: 298 NPDKLLWLNQHYIKHSDPDHVARHLSWHMGNHG--IDPSAPPPLREVVTAQRERAKTLAE 355 Query: 362 LVDHCAFALKTRPLALEEKTQKQLTEETVERLKRLRDQLAAAPDFDAATLETVLKSFAES 421 + + + + E+ +K LT + L+ L L A D+ A + ++ AE Sbjct: 356 MAANSVYFYRDFEDYEEKAARKNLTGDARPVLQALHAALEALGDWTAEAIHAAVEGVAER 415 Query: 422 EGVGFGKFGPALRGVLTGGAQAPDLNKTMAALSRDEAIGRLDDAL 466 + GK LR +TGG+ +P +++T+A L +D + R+ AL Sbjct: 416 LELKLGKVAQPLRVAVTGGSVSPPIDQTLALLGKDRTLARIGRAL 460 Lambda K H 0.319 0.135 0.405 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: 655 Number of extensions: 32 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: 470 Length of database: 470 Length adjustment: 33 Effective length of query: 437 Effective length of database: 437 Effective search space: 190969 Effective search space used: 190969 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 (21.7 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