Align Gamma aminobutyrate transaminase 3, chloroplastic; Gamma-aminobutyrate transaminase isozyme 3; LeGABA-TP3; SlGABA-T3; EC 2.6.1.96 (characterized)
to candidate WP_033100048.1 JG50_RS0105185 adenosylmethionine--8-amino-7-oxononanoate transaminase
Query= SwissProt::Q84P52 (520 letters) >NCBI__GCF_000763315.1:WP_033100048.1 Length = 450 Score = 256 bits (655), Expect = 9e-73 Identities = 141/433 (32%), Positives = 235/433 (54%), Gaps = 7/433 (1%) Query: 72 PFTAGWHSTDLEPLVIQKSEGSYVYDVNGKKYLDALAGLWCTSLGGNEPRLVAAATKQLN 131 PFT EPL+I++++G +YDV G++Y D A +W G N P L A QL Sbjct: 20 PFTQMKEYLQDEPLIIERADGVKLYDVQGREYYDGNASVWLNVHGHNHPALNEAIKVQLE 79 Query: 132 ELAFYHSFWNRSTKPSLDLAKELLDLFTANKMAKAFFTNSGSEANDTQVKLVWYYNNALG 191 ++A + + P++ LA+ L+ + T ++ K F+++SG+EA + +K+ + Y G Sbjct: 80 KVA-HSTLLGMGNIPAILLAERLVKI-TPTRLQKVFYSDSGAEAVEIGLKMAFQYWKNRG 137 Query: 192 RPDKKKFIARTKSYHGSTLISASLSGLPALHQQFDLPAPFVLHTDCPHFWRFHQPGETEE 251 P+K F++ YHG T+ + S+ G+ H FD + P+ +RF T E Sbjct: 138 FPEKNTFLSMKNGYHGDTVGAVSVGGMDLFHATFDRLLFSTIKLPYPYPYRFDG---TAE 194 Query: 252 EFSTRLANNLENLILKEGPETIAAFIAEP-VMGAGGVIPPPATYFEKVQAILKKYDILFI 310 E + LE+++ +G E IA I EP V GAGG+I P Y +V+ + ++YD+L + Sbjct: 195 ECKQACLHELESVLKSQG-ERIAGLIVEPMVQGAGGMIMMPPGYLSEVEKMCRQYDVLLL 253 Query: 311 ADEVICGFGRLGTMFGCEKYNIKPDLVSVAKALSSGYMPIGAVLVSPEVSDVIYSQSNKL 370 ADEV GFGR G MF CE ++PD++ V K L+ GY+P+ A L S EV D ++ ++ Sbjct: 254 ADEVATGFGRTGKMFACEHEGVQPDIMMVGKKLTGGYLPVAATLTSDEVYDAFFADHSEA 313 Query: 371 GTFSHGFTYSGHPVSCAVALETLKIYKERNIIEQVNRISPKFQEGLKAFSDSPIIGEIRG 430 TF HG +Y+G+ + CAVAL L +Y+ ++++ V S + L+A D P +GE+R Sbjct: 314 KTFFHGHSYTGNQLGCAVALANLDLYEREHLLDHVQEASRCLADHLEALKDLPAVGEVRQ 373 Query: 431 TGLLHGTEFTDNKSPNDPFPPEWGIGAYFGARCEKHGVLVRVAGDNIMMSPPYILSLEEI 490 G++ G E K +P+P IGA + + G++ R + + PP L ++ Sbjct: 374 LGMMVGIELVKEKETKEPYPFAEAIGAKVCRKARELGLVTRPLDHVVTLMPPLATPLPDL 433 Query: 491 DELIIKYGKALKD 503 ++ +A+++ Sbjct: 434 QAMVSILHEAIRE 446 Lambda K H 0.317 0.135 0.401 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: 576 Number of extensions: 20 Number of successful extensions: 5 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: 520 Length of database: 450 Length adjustment: 34 Effective length of query: 486 Effective length of database: 416 Effective search space: 202176 Effective search space used: 202176 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 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 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:
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