Align anthranilate synthase (subunit 1/2) (EC 4.1.3.27) (characterized)
to candidate Synpcc7942_1003 Synpcc7942_1003 anthranilate synthase, component I
Query= BRENDA::P20580 (492 letters) >FitnessBrowser__SynE:Synpcc7942_1003 Length = 517 Score = 383 bits (983), Expect = e-111 Identities = 230/500 (46%), Positives = 308/500 (61%), Gaps = 25/500 (5%) Query: 6 FLRLAADGYNRIPLSFETLADFDTPLSIYLKLA-DAPNSYLLESVQGGEKWGRYSIIGLP 64 F LA G N IP+ E +AD DTP+S + ++ D P S+LLESV+GGE GRYS +G Sbjct: 9 FASLAEQG-NFIPVYQEWVADLDTPVSAWYRICRDRPYSFLLESVEGGEHLGRYSFLGCD 67 Query: 65 CRTVLRVY-DHQVRISIDGVETERFDCADPLAFVEEFKARYQVPTVPGLPRFDGGLVGYF 123 VL D R DG +E DP A +++ A YQ +P LP GGL G++ Sbjct: 68 PLWVLEARGDRTTRRFRDG--SEEVFSGDPFAALKQCLAPYQPVHLPQLPSGVGGLFGFW 125 Query: 124 GYDCVRYVEKRLATCPNPDPLGNPDILLMVSDAVVVFDNLAGKIHAIVLAD----PSEEN 179 GY+ +R++E R+ + PD M D++++FD + +++AI AD P Sbjct: 126 GYELMRWIEPRVPVHSGGEN-DLPDGCWMQVDSLMIFDQVKRRLYAIAYADLQAEPDLHR 184 Query: 180 AYERGQARLEELLERLRQPITPRRG----LDLEAAQGREPAFRASFTREDYENAVGRIKD 235 AY R++EL+ R + ++ L ++A R ++++ T+E + V +D Sbjct: 185 AYALACNRVQELVNRFQGSLSASDRQLPWLPPQSAPSRPVDYQSNTTQEQFCANVLTAQD 244 Query: 236 YILAGDCMQVVPSQRMSIEFKAAPIDLYRALRCFNPTPYMYFFNFGDFHVVGSSPEVLVR 295 YI AGD QVV SQR++ + P DLYR+LR NP+PYM FF FGD+ ++GSSPEV+V+ Sbjct: 245 YIRAGDIFQVVLSQRLTTHYSGDPFDLYRSLRLINPSPYMAFFRFGDWQLIGSSPEVMVK 304 Query: 296 VEDG-------LVTVRPIAGTRPRGINEEADLALEQDLLSDAKEIAEHLMLIDLGRNDVG 348 E + TVRPIAGTRPRG D AL DLL+D KE+AEH+ML+DLGRND+G Sbjct: 305 AEQDPHQSDRQVATVRPIAGTRPRGRTAPEDAALATDLLADPKEVAEHVMLVDLGRNDLG 364 Query: 349 RVSDIGAVKVTEKMVIERYSNVMHIVSNVTGQLREGLSAMDALRAILPAGTLSGAPKIRA 408 RV + G+V+V E MVIERYS+VMHIVSNV G L A D LRA PAGT+SGAPKIRA Sbjct: 365 RVCEKGSVRVDELMVIERYSHVMHIVSNVVGLLDRDRDAWDLLRATFPAGTVSGAPKIRA 424 Query: 409 MEIIDELEPVKRGVYGGAVGYLAWNGNMDTAIAIRTAVIK-NGELH---VQAGGGIVADS 464 MEII ELE +RG Y GA GY + G ++TAI IRT +++ G H VQAG G+VADS Sbjct: 425 MEIIHELEGCRRGPYSGAYGYYDFEGQLNTAITIRTMIVQAEGSGHRVSVQAGAGVVADS 484 Query: 465 VPALEWEETINKRRAMFRAV 484 VP E+EET+NK R + A+ Sbjct: 485 VPIKEYEETLNKARGLLEAI 504 Lambda K H 0.321 0.139 0.408 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: 649 Number of extensions: 41 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: 492 Length of database: 517 Length adjustment: 34 Effective length of query: 458 Effective length of database: 483 Effective search space: 221214 Effective search space used: 221214 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: 52 (24.6 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