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_012406419.1 BPHY_RS36040 diaminobutyrate--2-oxoglutarate transaminase
Query= SwissProt::P22256 (426 letters) >NCBI__GCF_000020045.1:WP_012406419.1 Length = 422 Score = 174 bits (442), Expect = 4e-48 Identities = 125/415 (30%), Positives = 204/415 (49%), Gaps = 21/415 (5%) Query: 17 RGVGQIHPIFADRAENCRVWDVEGREYLDFAGGIAVLNTGHLHPKVVAAVEAQLK--KLS 74 R + P+ +A ++ V+GR Y+DF G LN GH HP + ++ L+ L Sbjct: 16 RTYSRAFPVVFCKARGAEIYSVDGRRYIDFLAGAGALNYGHNHPALKESIIEYLRGDNLV 75 Query: 75 HTC-FQVLAYEPYLELCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKIARAATKRSGTIA 133 H+ A YL+ + + K K L TG+ AVE A+++AR KRS ++ Sbjct: 76 HSLDLWTTAKYTYLDTFDRLILKTRRLDYKVHLTGPTGTNAVEAAIRLARKIKKRSTIVS 135 Query: 134 FSGAYHGRTHYTLALTGKVNPYSAGMGLMPGHVYRALYPCPLHGISEDDAIASIHRIFKN 193 F+ +HG T +LALTG SA G+ + G+ D + + + Sbjct: 136 FTNGFHGITMGSLALTGNAKFRSAAGLPSMGNAFMPFDNYFGKGV---DTLRYFKKCLSD 192 Query: 194 DAAPEDI-AAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLIADEVQSGAGRTGTLF 252 ++ D AA+++E VQGEGG +SP ++Q L +C + I+LI D++Q+G GRTG F Sbjct: 193 RSSGLDYPAAVIVEVVQGEGGINVASPGWLQELETVCRDQDILLIIDDIQAGCGRTGRFF 252 Query: 253 AMEQMGVAPDLTTFAKSIAG-GFPLAGVTGRAEVMDAVAPGGLGGTYAGNPIACVAALEV 311 + E GV PDL T +KS++G G P + V R E D G GT+ GN A + + Sbjct: 253 SFEHAGVVPDLVTNSKSLSGFGLPFSQVLIRPE-HDQWETGQYNGTFRGNNAAMITGAKA 311 Query: 312 LKVF-EQENLLQKANDLGQKLKDGLLAIAE--KHPEI-GDVRGLGAMIAIELFEDGDHNK 367 L+ F + + G+ +++G L + + ++ ++ + RGLG M I++ Sbjct: 312 LEYFWSDDAFADEVRRKGEIVREGFLGLTDLLRYRQVEAEERGLGLMRGIDV-------- 363 Query: 368 PDAKLTAEIVARARDKGLILLSCGPYYNVLRILVPLTIEDAQIRQGLEIISQCFD 422 L +I A A +GLI+ + G V++ L PL QI + ++I+ + D Sbjct: 364 QSGALATKITAEAFRQGLIIETSGHSGQVIKCLCPLVTTGDQIEEAMQILRRSID 418 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: 415 Number of extensions: 23 Number of successful extensions: 5 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: 422 Length adjustment: 32 Effective length of query: 394 Effective length of database: 390 Effective search space: 153660 Effective search space used: 153660 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