Align Anthranilate synthase component 1 2; EC 4.1.3.27; Anthranilate synthase component I 2 (uncharacterized)
to candidate N515DRAFT_2823 N515DRAFT_2823 anthranilate synthase component 1
Query= curated2:Q9HS66 (488 letters) >lcl|FitnessBrowser__Dyella79:N515DRAFT_2823 N515DRAFT_2823 anthranilate synthase component 1 Length = 449 Score = 236 bits (602), Expect = 1e-66 Identities = 175/410 (42%), Positives = 219/410 (53%), Gaps = 47/410 (11%) Query: 80 GALDTVQAAVGA-RLARVGCD-VPHPGGLFGWLSYDIARELEAIPDTTTDARGLPRLQLG 137 G L + AA A RL R D +P GG +L+Y++A E+E PRL+L Sbjct: 71 GFLHALDAAWQAERLPRDADDGLPFHGGWVLFLAYELAGEIE------------PRLRLA 118 Query: 138 ---VYPTIAAWREPFTPGDDLRLIAAVPVD---EYTPDGAFEAGRDRVQSLAAAIRDGDP 191 V P A R P AA VD E T A D ++ +AA D Sbjct: 119 PHEVLPVALALRCP----------AAAIVDHERERTVLIAEPGCEDLLEQMAA-----DL 163 Query: 192 AVGPPPADSPAPFE-SVAGRAAFESRVRRIQDAIRDGDTFQANVSHR-----LDAPAAVH 245 PP A PAP E F V RI + + GD FQ N+S DAP Sbjct: 164 EAQPPIAPLPAPLERDEDDPQLFRDGVARIHEHLHAGDIFQVNLSRAWRARFADAPT--- 220 Query: 246 PVAVFEALRDTNPAPYSGIVEFPGVDLVSASPELLLARRGRELTTEPIAGTRPRGATPAE 305 P +++ +LR NPAP++G+++ P +VS+SPE L+ RG T PIAGTRPR TPA+ Sbjct: 221 PASLYASLRMANPAPFAGLLQQPDWAVVSSSPERLVEARGGVAQTRPIAGTRPR--TPAD 278 Query: 306 DDAARAA-LRADDKERAEHAMLVDLERNDLGKVSEYGSVAVPDYRRVDAYSEVLHLVSEV 364 D+ AR LR KERAEH ML+DLERNDLG+V GSV V + V++Y+ V H+VS V Sbjct: 279 DELARIRELRTHPKERAEHVMLIDLERNDLGRVCVPGSVQVDELMVVESYAHVHHIVSNV 338 Query: 365 TGRLRDSCSLRDAIAAVFPGGTITGAPKPRTMALIDTVEATRRGPYTGSLAAIGFDGDAT 424 G+LR + IAA FPGGTITG PK R M +I +E RG YTG+L + +GD Sbjct: 339 RGKLRPGVTPGQVIAATFPGGTITGCPKVRCMEIIHALEDAPRGAYTGALGYLDRNGDLD 398 Query: 425 LSITIRTLVRRAATYHLRVGAGIVHDSTPAAEYDETLAKARALVTALGDA 474 L+I IRTL LR GAGIV DS E DET AKAR L+ ALG A Sbjct: 399 LNILIRTLTLAGTQVSLRAGAGIVADSVAEKELDETRAKARGLLRALGVA 448 Lambda K H 0.317 0.135 0.397 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: 614 Number of extensions: 37 Number of successful extensions: 4 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: 488 Length of database: 449 Length adjustment: 33 Effective length of query: 455 Effective length of database: 416 Effective search space: 189280 Effective search space used: 189280 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 (21.7 bits) S2: 51 (24.3 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