Align Anthranilate synthase component I (characterized, see rationale)
to candidate WP_066328935.1 BLR17_RS13350 anthranilate synthase component I family protein
Query= uniprot:A0A1X9ZB07_9SPHI (466 letters) >NCBI__GCF_900100165.1:WP_066328935.1 Length = 466 Score = 524 bits (1349), Expect = e-153 Identities = 259/467 (55%), Positives = 352/467 (75%), Gaps = 7/467 (1%) Query: 3 YKINTTYKKMLADTTTPVSIYLRLRDVYPNSILLESSDYHSRENSMSFVCADPVAGIILK 62 +K+NT +K++LADT TPVS+Y ++RD +PNS+LLESSDYH+ +NS S++C +P+A I ++ Sbjct: 4 FKLNTKFKQILADTITPVSVYFKIRDKFPNSLLLESSDYHANDNSFSYICCNPIASIKIE 63 Query: 63 GSRLETYFPDGAVEITE---SKNLIEEITDFKDKFSETELPEIKFISSGLFGYFTWNAVQ 119 + FPDG+ E T N+ E I F +F ++E KFI++GLFGY +++AV+ Sbjct: 64 NETIFKQFPDGSSETTTIDAKTNIPEVIQQFSGQF-KSEKNNFKFINNGLFGYISYDAVR 122 Query: 120 HFEDIKFTSETPEGEEIPEMQYHLYRYIIAIDHFKNEITLFKNTFEGEEEGGLEKMEYLI 179 +FE + + IP++ Y +Y+ IIAI+HFKNE +F ++ + ++ + ++E L+ Sbjct: 123 YFEKVTIAKKE-NSNTIPDLFYAVYQNIIAINHFKNEAYIFCHSVD--DKNNIAEIEQLM 179 Query: 180 QNKNYPEYKFQLRGEESSNLTDQGFMDLVEKLQKHIYRGDVFQIVPSRAFKQAFSGDEFN 239 Q++N P YKF GE SNLTD+ F V +KH +RGDVFQ+V SR F Q F GDEFN Sbjct: 180 QSRNIPSYKFSKEGEGFSNLTDEEFKHNVALAKKHCFRGDVFQLVLSRRFTQGFKGDEFN 239 Query: 240 VYRCLRSINPSPYLFYFDYGNFKLFGSSPEAQITIKNNSANIFPIAGTFKRSGNDIEDAE 299 VYR LRSINPSPYLF+FDYG+FK+FGSSPEAQI +K+ A I PIAGTF+R+G+D +DA Sbjct: 240 VYRALRSINPSPYLFFFDYGDFKIFGSSPEAQIIVKDRKAEIHPIAGTFRRTGDDEKDAV 299 Query: 300 QARKLEQDPKESAEHVMLVDLARNDLSRHCNRVEVKSFKEVQYYSHLIHLVSKVSGHLQE 359 A+KL +D KE++EHVMLVDLARNDLSRH + V V+ ++EVQ++SH+IHLVSKV+GHL + Sbjct: 300 LAKKLSEDKKENSEHVMLVDLARNDLSRHGHNVNVERYREVQFFSHVIHLVSKVTGHLHD 359 Query: 360 NVSAFKVVADTYPAGTLSGAPKYKAMQLIDENEKLGRNFYAGAIGFMGFNEDFNHAIMIR 419 + + +VVADT+PAGTLSGAPK++AMQLI++ EK RNFY GAIGFM F +FNHAIMIR Sbjct: 360 DATTMQVVADTFPAGTLSGAPKHRAMQLIEDYEKTNRNFYGGAIGFMDFEGNFNHAIMIR 419 Query: 420 TFMSKNNELHYRAGAGIVADSVPETEMQEVNNKIAALRKAVQMAEGI 466 TF+SKN++LH +AGAGIVA S E+EMQEV NK+ AL A+ +AE I Sbjct: 420 TFLSKNHQLHSQAGAGIVASSDEESEMQEVYNKLRALNAALDLAETI 466 Lambda K H 0.318 0.135 0.386 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: 764 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: 466 Length of database: 466 Length adjustment: 33 Effective length of query: 433 Effective length of database: 433 Effective search space: 187489 Effective search space used: 187489 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 Jul 26 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