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_034271648.1 AMYHA_RS14115 aspartate aminotransferase family protein
Query= SwissProt::P22256 (426 letters) >NCBI__GCF_000504245.1:WP_034271648.1 Length = 455 Score = 201 bits (510), Expect = 5e-56 Identities = 139/431 (32%), Positives = 211/431 (48%), Gaps = 36/431 (8%) Query: 21 QIHPIFADRAENCRVWDVEGREYLDFAGGIAVLNTGHLHPKVVAAVEAQLKKLSHTCFQV 80 ++ P+ +AE VWD +G LDF + N GH HP +V AV+ Q L T Sbjct: 31 KLDPMVVTKAEGAYVWDRDGNRLLDFTSQLVFTNLGHQHPAIVRAVQDQAATLC-TVAPN 89 Query: 81 LAYEPYLELCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKIARAATKRSGTIAFSGAYHG 140 E ++ PGD + G++A E+A+++AR T RS ++ +YHG Sbjct: 90 HVNGARSEAARLIAAHTPGDL-NRVFFTNGGADANEHAIRMARLHTGRSKVLSTYRSYHG 148 Query: 141 RTHYTLALTGKVNPYSAGMG------LMPGHVYRALYPCPLHGISEDDAIASIHRIFKND 194 T + +TG+ +S G +YR+ + A+A + ++ + Sbjct: 149 GTDLAVNVTGEPRRWSNDTGSAGVVHFFGPFLYRSAFSATTEEEECQRALAHLEQVITLE 208 Query: 195 AAPEDIAAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLIADEVQSGAGRTGTLFAM 254 P IAAI++E + G G P ++ +R LCD GI+ IADEV SG GR GT FA+ Sbjct: 209 G-PSTIAAIMLESIPGTAGIMVPPPGYLAGVRELCDRFGIVFIADEVMSGFGRAGTWFAI 267 Query: 255 EQMG------VAPDLTTFAKSIAGGF-PLAGVTGRAEVMDAVA----PGGLGGTYAGNPI 303 E V PDL TFAK + G+ PL GV + A PGGL TY+G+P+ Sbjct: 268 EHGSAGSAGPVVPDLLTFAKGVNSGYVPLGGVAINEAIYSTFAERPYPGGL--TYSGHPL 325 Query: 304 ACVAALEVLKVFEQENLLQKANDLGQKL-KDGLLAIAEKHPEIGDVRGLGAMIAIELFED 362 AC AA+ ++ E + L++ A LG+ + GL +A +H IG+VRG G AIEL D Sbjct: 326 ACAAAVATIETMENDGLVEHAAALGEDVFGPGLRELAARHDWIGEVRGTGVFWAIELVAD 385 Query: 363 GDHNKP------DAKLTAEIVARARDKGLILLSCGPYYNVLRI--LVPLTIEDAQIRQGL 414 +P ++ +E+VA R +GL+ P+ N RI + P+T + R+G+ Sbjct: 386 QATREPLAPYGGTSEAMSEVVAACRRRGLL-----PFVNFNRIHAVPPMTTTAEEAREGI 440 Query: 415 EIISQCFDEAK 425 EI+ E + Sbjct: 441 EILDAALTEVR 451 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: 521 Number of extensions: 19 Number of successful extensions: 7 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: 455 Length adjustment: 32 Effective length of query: 394 Effective length of database: 423 Effective search space: 166662 Effective search space used: 166662 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 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