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_034269313.1 AMYHA_RS07330 4-aminobutyrate--2-oxoglutarate transaminase
Query= SwissProt::P22256 (426 letters) >NCBI__GCF_000504245.1:WP_034269313.1 Length = 442 Score = 367 bits (941), Expect = e-106 Identities = 195/416 (46%), Positives = 250/416 (60%), Gaps = 4/416 (0%) Query: 4 NKELMQRRSQAIPRGVGQIHPIFADRAENCRVWDVEGREYLDFAGGIAVLNTGHLHPKVV 63 ++ L QRR+ A+ GVG + P + A + D +G +D GIAV N GH P VV Sbjct: 19 SRALHQRRTSAVAAGVGSVLPAYVTSANGGLLTDADGNTLIDLGSGIAVTNVGHAAPAVV 78 Query: 64 AAVEAQLKKLSHTCFQVLAYEPYLELCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKIAR 123 V Q ++ +HTCF V YE Y+E+CE +NQ PGD K+++L +G+EAVENAVKIAR Sbjct: 79 ERVREQAERFTHTCFMVTPYEGYVEVCETLNQLTPGDHEKRSVLFNSGAEAVENAVKIAR 138 Query: 124 AATKRSGTIAFSGAYHGRTHYTLALTGKVNPYSAGMGLMPGHVYRA--LYPCPLHGISED 181 AT R + F AYHGRT+ T+ALT K PY G G VYR YPC E Sbjct: 139 VATGRQAVVVFDHAYHGRTNLTMALTAKSVPYKHGFGPFAPEVYRVPGSYPCHDGLTGEQ 198 Query: 182 DAIASIHRIFKNDAAPEDIAAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLIADEV 241 A A+I RI K + +AA+VIEP+QGEGGF +P F+ L C +G + +ADEV Sbjct: 199 AAAAAIDRIEKQ-LGGDSVAAVVIEPIQGEGGFIEPAPGFLSALSRWCTANGAVFVADEV 257 Query: 242 QSGAGRTGTLFAMEQMGVAPDLTTFAKSIAGGFPLAGVTGRAEVMDAVAPGGLGGTYAGN 301 Q+G RTG FA E V PDL AK IAGG PLA VTGRAE+MDAV PGGLGGTY GN Sbjct: 258 QTGFCRTGAWFACEHEDVVPDLVATAKGIAGGLPLAAVTGRAELMDAVPPGGLGGTYGGN 317 Query: 302 PIACVAALEVLKVFEQENLLQKANDLGQKLKDGLLAIAEKHPEIGDVRGLGAMIAIELFE 361 PIAC A L ++ ENL A +G + L A+AE+ IGDVRG GAM+A+E Sbjct: 318 PIACAAGLGAIETMRTENLADAARSIGDMVLPRLRALAEETGVIGDVRGRGAMLAVEFVR 377 Query: 362 DGDHNKPDAKLTAEIVARARDKGLILLSCGPYYNVLRILVPLTIEDAQIRQGLEII 417 G H +PD +T I G+++L+CG Y NV+R+L PLT+ + +GL + Sbjct: 378 PGTH-EPDPDITKRIATACHAAGVVVLTCGTYGNVVRLLPPLTLPADLLDEGLSAL 432 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: 548 Number of extensions: 31 Number of successful extensions: 3 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: 442 Length adjustment: 32 Effective length of query: 394 Effective length of database: 410 Effective search space: 161540 Effective search space used: 161540 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