Align Aromatic-amino-acid aminotransferase (EC 2.6.1.57) (characterized)
to candidate H281DRAFT_01667 H281DRAFT_01667 DNA-binding transcriptional regulator, MocR family, contains an aminotransferase domain
Query= reanno::acidovorax_3H11:Ac3H11_1015 (396 letters) >FitnessBrowser__Burk376:H281DRAFT_01667 Length = 409 Score = 321 bits (823), Expect = 2e-92 Identities = 175/397 (44%), Positives = 248/397 (62%), Gaps = 10/397 (2%) Query: 2 QFADRLNNVETSAIRELFKLLGKPGIISFAGGFPDSAMFDVEGIRAASNAALAEEPGAAL 61 +F + S IRELFK L +PG+ISFAGG+P S +FDV+G+ +A A L Sbjct: 3 EFTAPFQDPSGSPIRELFKYLAEPGMISFAGGYPASDLFDVDGLASAQKRAYRNS-NRCL 61 Query: 62 QYGATEGYNPLREQLAAFMTSKGAKDVAADNLIVTTGSQQALDLLGKTLISPGDKVIVEG 121 QYG T+G L+ +L M +G + L+VTTGSQQ LDLL + L++PGD V+ E Sbjct: 62 QYGPTDGLPELKSELVNLMARRGVTCEPGE-LLVTTGSQQGLDLLLRVLVAPGDVVVTEQ 120 Query: 122 PTFLATIQCFRLYGAELISAPIDGNGVKTDELEKLI---AEHKPKFVYLIPTFGNPSGAM 178 P + AT+Q +L A++++A +DG+G+ + L + A +PK +Y +PTF NP+GA Sbjct: 121 PAYPATLQALKLQHAQIVTAQVDGHGIDVENLAAHLESGAVPRPKLLYTVPTFANPTGAT 180 Query: 179 LSLERRKAVLEMAVKHNTLIVEDDPYGDLYFGDAPPPSLLNLSATVPGSRELLVHCGSLS 238 ++ ERR +L++AVK+ +IVEDDPYGDL F PS+L L+A V GSR+ +VH SLS Sbjct: 181 ITRERRIELLKLAVKYRFVIVEDDPYGDLRFSGDTVPSILALTAEVEGSRDWVVHFASLS 240 Query: 239 KVLSPGLRVGWMIAPAELLGKATMCKQFSDAHTSTFAQATAAQYLKAGRMPGTLANVRKV 298 K+++PG+RVGW IAPAE+ + + KQ D ++ + QA AA+YL G + L + Sbjct: 241 KIVAPGVRVGWSIAPAEITRRCVIAKQTVDLCSAPWTQAIAAEYLADGALERHLPRITTT 300 Query: 299 YAERAQAMGDALRKELGDAIEFVQPQGGLFVWARLTGAGGKVADGNVLAKRAIEKGVAFV 358 Y + A+ + LR +L DAI+F QP+GG+FVWAR+ G D + L AIE V FV Sbjct: 301 YRRKCDALCNELRWQLDDAIQFHQPEGGMFVWARIEG-----IDSSELLWHAIENKVIFV 355 Query: 359 PGTPFFCANPDHATFRLSFATADVDKIREGVARLGQA 395 PG FF D A+ RLSFA V++I+EG RL +A Sbjct: 356 PGKAFFADKLDVASLRLSFAAPGVEEIQEGARRLKRA 392 Lambda K H 0.319 0.136 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: 484 Number of extensions: 23 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: 396 Length of database: 409 Length adjustment: 31 Effective length of query: 365 Effective length of database: 378 Effective search space: 137970 Effective search space used: 137970 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: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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