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_011779798.1 MVAN_RS12965 4-aminobutyrate--2-oxoglutarate transaminase
Query= SwissProt::P22256 (426 letters) >NCBI__GCF_000015305.1:WP_011779798.1 Length = 446 Score = 352 bits (903), Expect = e-101 Identities = 189/420 (45%), Positives = 256/420 (60%), Gaps = 9/420 (2%) Query: 6 ELMQRRSQAIPRGVGQIHPIFADRAENCRVWDVEGREYLDFAGGIAVLNTGHLHPKVVAA 65 EL+ R+S A+ RGVG P++A RA V DV+G +D GIAV G+ PKVV Sbjct: 21 ELIARKSAAVARGVGTTMPVYAARAFGGIVEDVDGNRLIDLGSGIAVTTIGNASPKVVER 80 Query: 66 VEAQLKKLSHTCFQVLAYEPYLELCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKIARAA 125 QL K +HTCF V YE Y+ + E +N+ PGD K+T L +GSEAVENAVKIAR+ Sbjct: 81 AAEQLHKFTHTCFMVTPYEGYVAVAEALNRLTPGDGDKRTALFNSGSEAVENAVKIARSY 140 Query: 126 TKRSGTIAFSGAYHGRTHYTLALTGKVNPYSAGMGLMPGHVYRALYPCPLHG------IS 179 T++ ++F AYHGRT+ T+ALT K PY G G +YRA P ++ Sbjct: 141 TRKQAVVSFDHAYHGRTNLTMALTAKSMPYKHGFGPFAPEIYRAPLSYPFRDAEFGKELA 200 Query: 180 EDDAIASIHRIFKND--AAPEDIAAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLI 237 D +A+ I D +++AA++IEP+QGEGGF + F+ L C +G++ I Sbjct: 201 TDGELAARRAITVIDKQVGADNLAAVIIEPIQGEGGFIVPAEGFLPTLLEWCHANGVVFI 260 Query: 238 ADEVQSGAGRTGTLFAMEQMGVAPDLTTFAKSIAGGFPLAGVTGRAEVMDAVAPGGLGGT 297 ADEVQ+G RTG +FA E G+ PDL AK IA G PL+ VTGRAE+MDA GLGGT Sbjct: 261 ADEVQTGFARTGAMFACEHEGIVPDLIVTAKGIADGMPLSAVTGRAEIMDAPHVSGLGGT 320 Query: 298 YAGNPIACVAALEVLKVFEQENLLQKANDLGQKLKDGLLAIAEKHPEIGDVRGLGAMIAI 357 Y GNP+AC AAL ++ E + L+ +A + +KD L + + IGDVRG GAMIA+ Sbjct: 321 YGGNPVACAAALATIETIESDGLVARAAQIETLMKDKLGRLQAEDDRIGDVRGRGAMIAV 380 Query: 358 ELFEDGDHNKPDAKLTAEIVARARDKGLILLSCGPYYNVLRILVPLTIEDAQIRQGLEII 417 EL + G +PD +LT ++A A G+I+LSCG + NVLR L PL I D + +GL+++ Sbjct: 381 ELVKPGT-LEPDPELTKNLLAAAHRAGVIVLSCGTFGNVLRFLPPLAISDELLLEGLDVL 439 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: 514 Number of extensions: 26 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: 446 Length adjustment: 32 Effective length of query: 394 Effective length of database: 414 Effective search space: 163116 Effective search space used: 163116 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