Align 4-aminobutyrate aminotransferase GabT; 5-aminovalerate transaminase; GABA aminotransferase; GABA-AT; Gamma-amino-N-butyrate transaminase; GABA transaminase; Glutamate:succinic semialdehyde transaminase; L-AIBAT; EC 2.6.1.19; EC 2.6.1.48 (characterized)
to candidate WP_068107728.1 I601_RS07035 aspartate aminotransferase family protein
Query= SwissProt::P22256 (426 letters) >NCBI__GCF_001653335.1:WP_068107728.1 Length = 454 Score = 217 bits (553), Expect = 5e-61 Identities = 145/425 (34%), Positives = 218/425 (51%), Gaps = 29/425 (6%) Query: 21 QIHPIFADRAENCRVWDVEGREYLDFAGGIAVLNTGHLHPKVVAAVEAQLKKLSHTCFQV 80 QI P+ A WD G +YLDF+ + +N G+ HP++VAA++ +L T Sbjct: 32 QIDPLPIAAALGSHFWDYAGTKYLDFSSQLVNVNIGYQHPRLVAAIQEYAGRLC-TVAPP 90 Query: 81 LAYEPYLELCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKIARAATKRSGTIAFSGAYHG 140 A + E ++ PG K G++A E+AV++AR T RS +A +YHG Sbjct: 91 FANDMRSEAARLLADLAPGTL-NKVFFTNGGADANEHAVRMARLHTGRSKVLAAYRSYHG 149 Query: 141 RTHYTLALTGKVNPYSAGMGLMPGHVY---RALYPCPLHG--ISEDDAIASIH-RIFKND 194 T + +TG + A GL PG V+ Y H + E+ A A H R Sbjct: 150 ATAGAITMTGDPRRWGAEPGL-PGVVHFWGPYPYRSAFHSSDVEEEGARALQHLRDTIMV 208 Query: 195 AAPEDIAAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLIADEVQSGAGRTGTLFAM 254 P IAA+V+E V G G P +++ +R +CDEHGI+L+ADEV SG GR G FA+ Sbjct: 209 EGPGTIAAVVLETVVGTNGILVPPPGYLEGVRQICDEHGILLVADEVMSGFGRCGEWFAV 268 Query: 255 EQMGVAPDLTTFAKSIAGGF-PLAGV----TGRAEVMDAVAPGGLGGTYAGNPIACVAAL 309 + + PDL TFAK + G+ P+ GV T A D PGGL TY+G+P+AC +A+ Sbjct: 269 DHWAITPDLITFAKGVNSGYVPIGGVLISDTVAATFDDRAYPGGL--TYSGHPLACASAV 326 Query: 310 EVLKVFEQENLLQKANDLGQKLKDGLLA-IAEKHPEIGDVRGLGAMIAIELFEDGDHNKP 368 + + +E +++ A DLG + LA +AE HP +GDVRGLG A+EL D D +P Sbjct: 327 ASMTIMREEGIVEHARDLGTDVIGPALAKLAENHPSVGDVRGLGVFWALELVRDRDTREP 386 Query: 369 ---------DAKLTAEIVARARDKGLILLSCGPYYNVLRILVPLTIEDAQIRQGLEIISQ 419 DA E+ A + +GL ++N + ++ P T ++ +G+E++ + Sbjct: 387 LVPYNASGSDAAPMGEVAAECKRRGLWPF---VHFNRVHVVPPCTTTADEVLEGIEVLDE 443 Query: 420 CFDEA 424 A Sbjct: 444 ALGVA 448 Lambda K H 0.320 0.137 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: 525 Number of extensions: 30 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: 426 Length of database: 454 Length adjustment: 32 Effective length of query: 394 Effective length of database: 422 Effective search space: 166268 Effective search space used: 166268 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: 51 (24.3 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