Align glutamate N-acetyltransferase (EC 2.3.1.35) (characterized)
to candidate WP_072905012.1 BUB13_RS01680 bifunctional glutamate N-acetyltransferase/amino-acid acetyltransferase ArgJ
Query= BRENDA::Q92MJ1 (413 letters) >NCBI__GCF_900142125.1:WP_072905012.1 Length = 397 Score = 308 bits (790), Expect = 1e-88 Identities = 176/399 (44%), Positives = 250/399 (62%), Gaps = 6/399 (1%) Query: 15 EMPALRGVRMATAAAGIKYKNRTDVLMMLFDRPASVAGVFTRSKCPSAPVDHCRQNLPGG 74 ++PA G R A A+GIK + D+ ++ D+PA+ AGVFT++K +AP+ + + GG Sbjct: 5 DIPA--GFRFAGLASGIKKSGKLDLALICSDQPAATAGVFTQNKVYAAPLQVTKPRIAGG 62 Query: 75 IARAVVVNSGNANAFTGKKGREATRLTAEAAAKAVGCSEAEVFLASTGVIGEPLDATKFA 134 + +AV++NSGNANA TG+ G + + T++ AK + E V LASTGVIG L F Sbjct: 63 VCQAVLINSGNANACTGEAGLQVAQQTSQLVAKQLNIDEELVALASTGVIGVQLPIIPFE 122 Query: 135 GVLDKLAASATQDFWFEAAKAIMTTDTYPKVATRSAEIGGVKVAINGIAKGAGMIAPDMA 194 +DKL + +D A+AIMTTD Y KVA+ G I G+AKGAGMI P+MA Sbjct: 123 QNMDKLVDALAEDRALVVAEAIMTTDAYSKVASARFSDGEKAYNILGLAKGAGMIHPNMA 182 Query: 195 TMLSFVVTDADIAPAALQALLQAGVEPTFNSVTVDSDTSTSDTLMLFATGAAAGDGQAKV 254 TML FV+TDA I L + L+ V+ +FNS+TVD DTST+DT++L A GAA G K+ Sbjct: 183 TMLGFVLTDAAIDAQFLDSALRQAVKKSFNSITVDGDTSTNDTVLLLANGAAGG---KKI 239 Query: 255 EDAADPRLDGFRAALDDLLRDLALQVVRDGEGARKMVEVTVEGAENDAAAKRIALSIANS 314 E ++ F L+ +L DLA +VRDGEGA K+VE+ V+GAE++ AA+ A S+A S Sbjct: 240 EPGSE-AAQAFVQHLERVLLDLAKMIVRDGEGATKLVEIKVQGAESEDAARTAAKSVATS 298 Query: 315 PLVKTAVAGEDANWGRVVMAVGKSGEMAERDRLAIWFGDIRVAVEGERDPAYSEAAATAV 374 LVKTA GEDANWGR++ AVG SG +++++ I+F + V +G EA AT V Sbjct: 299 SLVKTAFFGEDANWGRIISAVGYSGIDVDQNKIDIFFNQVAVTKDGLSTGPELEAEATEV 358 Query: 375 MQGETIPIRVDIGLGSGRATVYTCDLTKEYVEINGDYRS 413 ++ + V++ G ++ YT DL EY++IN DYR+ Sbjct: 359 LKLPEFTVTVELNQGDTCSSYYTSDLGYEYIKINADYRT 397 Lambda K H 0.316 0.130 0.365 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: 350 Number of extensions: 9 Number of successful extensions: 2 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: 413 Length of database: 397 Length adjustment: 31 Effective length of query: 382 Effective length of database: 366 Effective search space: 139812 Effective search space used: 139812 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: 50 (23.9 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