Align 2-aminoadipate transaminase (EC 2.6.1.39) (characterized)
to candidate AZOBR_RS06555 AZOBR_RS06555 GntR family transcriptional regulator
Query= BRENDA::Q72LL6 (397 letters) >FitnessBrowser__azobra:AZOBR_RS06555 Length = 404 Score = 320 bits (819), Expect = 6e-92 Identities = 173/403 (42%), Positives = 250/403 (62%), Gaps = 12/403 (2%) Query: 4 LSWSEAFGKGAGRIQASTIRELLKLTQRPGILSFAGGLPAPELFPKEEAAEAAARILREK 63 + W F + AS IRELLKL +RP I+SFAGG+P P+ FP A A +I + Sbjct: 3 VDWGNVFAGRVAGMGASEIRELLKLLERPEIISFAGGIPDPDFFPTAAIARAYEKIFQSN 62 Query: 64 GEV--ALQYSPTEGYAPLRAFVAEWIGVRP-----EEVLITTGSQQALDLVGKVFLDEGS 116 ALQY+ +EG+ PLR ++ ++G R +EVL+T+GSQQAL+ VGK+ + G Sbjct: 63 SGAGGALQYTISEGFTPLREWICAYLGRRGIQAGLDEVLVTSGSQQALEFVGKLLIGPGE 122 Query: 117 PVLLEAPSYMGAIQAFRLQGPRFLTVPAGEEGPDLDALEEVLKRERPRFLYLIPSFQNPT 176 +L+ P+Y+GA+QAF P++L+VP EGPDL A+E L+ ++P+F YL+P FQNP Sbjct: 123 KILVTRPTYLGALQAFSPYEPQYLSVPGDAEGPDLAAVEAALE-QKPKFFYLVPDFQNPN 181 Query: 177 GGLTPLPARKRLLQMVMERGLVVVEDDAYRELYFGEARLPSLFEL--AREAG-YPGVIYL 233 G L R+ LL + + G+ +VED AY EL + +PS+ L AR G V++ Sbjct: 182 GTTISLARREALLDLCAKHGVPIVEDAAYTELRYEGEPIPSMVALDAARNGGKITNVLFC 241 Query: 234 GSFSKVLSPGLRVAFAVAHPEALQKLVQAKQGADLHTPMLNQMLVHELLKEGFSERLERV 293 GSFSK + P LRV + E + +LV KQ DLHT +NQ+++H+++ + F + R+ Sbjct: 242 GSFSKTMVPALRVGWINGPAEVINRLVLMKQAGDLHTSTINQIVLHDVVSQNFDSHIRRL 301 Query: 294 RRVYREKAQAMLHALDREVPKEVRYTRPKGGMFVWMELPKGLSAEGLFRRALEE-NVAFV 352 R Y+E+ AML AL P V +T+P+GGMFVW+ELP+G L RA+++ NVAFV Sbjct: 302 RAGYKERRDAMLTALSEFAPAGVTWTKPEGGMFVWIELPEGTDGVDLLARAIKDANVAFV 361 Query: 353 PGGPFFANGGGENTLRLSYATLDREGIAEGVRRLGRALKGLLA 395 PG F A+ G+NTLRLS++ + E I EG+RRL L+ + A Sbjct: 362 PGSAFHADRSGKNTLRLSFSNNNPERIREGIRRLCGLLQTVAA 404 Lambda K H 0.320 0.139 0.403 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: 510 Number of extensions: 21 Number of successful extensions: 6 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: 397 Length of database: 404 Length adjustment: 31 Effective length of query: 366 Effective length of database: 373 Effective search space: 136518 Effective search space used: 136518 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: 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