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_012404126.1 BPHY_RS24335 4-aminobutyrate--2-oxoglutarate transaminase
Query= SwissProt::P22256 (426 letters) >NCBI__GCF_000020045.1:WP_012404126.1 Length = 430 Score = 460 bits (1184), Expect = e-134 Identities = 221/422 (52%), Positives = 296/422 (70%) Query: 2 NSNKELMQRRSQAIPRGVGQIHPIFADRAENCRVWDVEGREYLDFAGGIAVLNTGHLHPK 61 ++N +L+ R++ A PRGVG + +A RAEN +WDVEGR ++DFA GIAV NTGH HPK Sbjct: 3 DTNADLLDRKNAATPRGVGVMCEFYAARAENAELWDVEGRRFIDFAAGIAVCNTGHRHPK 62 Query: 62 VVAAVEAQLKKLSHTCFQVLAYEPYLELCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKI 121 +VAA+ QL +HT +Q++ Y Y+ L E +N++ PG++ KKT TTG+EAVENA+KI Sbjct: 63 IVAAIREQLDFFTHTAYQIVPYASYVTLAEKINERAPGNYPKKTAFFTTGAEAVENAIKI 122 Query: 122 ARAATKRSGTIAFSGAYHGRTHYTLALTGKVNPYSAGMGLMPGHVYRALYPCPLHGISED 181 ARAAT RSG IAF+G +HGRT +ALTGKV PY G P V+ A +P PLHG++ Sbjct: 123 ARAATGRSGVIAFTGGFHGRTMMGMALTGKVAPYKLNFGPFPAEVFHAPFPNPLHGVTTT 182 Query: 182 DAIASIHRIFKNDAAPEDIAAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLIADEV 241 D++ +I +FK D P+ +AAI+ EPVQGEGGF+ + F++ LR LCDEHGI+LIADEV Sbjct: 183 DSLKAIEHLFKADIEPKRVAAIIFEPVQGEGGFHPAPAEFVRALRKLCDEHGILLIADEV 242 Query: 242 QSGAGRTGTLFAMEQMGVAPDLTTFAKSIAGGFPLAGVTGRAEVMDAVAPGGLGGTYAGN 301 Q+G RTG LFAM+ V PDL T AKS+AGG PL+GV GRAE+MDA APGGLGGTYAGN Sbjct: 243 QTGFARTGKLFAMQHYDVVPDLMTMAKSLAGGMPLSGVVGRAELMDAAAPGGLGGTYAGN 302 Query: 302 PIACVAALEVLKVFEQENLLQKANDLGQKLKDGLLAIAEKHPEIGDVRGLGAMIAIELFE 361 P+A AA VL + ++E L +A LG ++K L + E P+I D+RG GAM+A+E + Sbjct: 303 PLAIAAAHAVLDIIDEEALCDRATQLGDRIKANLKNLREIVPQIADIRGPGAMVAVEFCK 362 Query: 362 DGDHNKPDAKLTAEIVARARDKGLILLSCGPYYNVLRILVPLTIEDAQIRQGLEIISQCF 421 G ++PD T ++ A+A ++GL+LL CG Y NV+R L PLT+E+ + L I+ Sbjct: 363 PGSEHEPDPTFTKQVQAKALERGLLLLVCGTYANVIRFLFPLTVEENVFDEALSILQDVL 422 Query: 422 DE 423 E Sbjct: 423 KE 424 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: 596 Number of extensions: 24 Number of successful extensions: 1 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: 430 Length adjustment: 32 Effective length of query: 394 Effective length of database: 398 Effective search space: 156812 Effective search space used: 156812 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 25 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