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_008509293.1 BIBO1_RS15460 aspartate aminotransferase family protein
Query= SwissProt::P22256 (426 letters) >NCBI__GCF_000182725.1:WP_008509293.1 Length = 452 Score = 168 bits (426), Expect = 3e-46 Identities = 133/425 (31%), Positives = 203/425 (47%), Gaps = 27/425 (6%) Query: 24 PIFADRAENCRVWDVEGREYLDFAGGIAVLNTGHLHPKVVAAVEAQLKKLSH-TCFQVLA 82 P + E V D+ G++ LD GG+ +N G+ V A+ QL L + + F+ Sbjct: 30 PRIVNGGEGVEVIDIHGKKVLDAVGGLWNVNLGYSCEPVKKAIRDQLDSLPYYSTFRGTT 89 Query: 83 YEPYLELCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKIARAATKRSGT------IAFSG 136 P +EL + + D + + GS++VE A+++AR K +G ++ Sbjct: 90 NSPLIELSYELAEFFKEDGLTRAFFTSGGSDSVETALRLARQFHKINGQPERTKFVSLKK 149 Query: 137 AYHGRTHYTLALTGKVNPYSAGMGLMPGHVYRALYPCPLHG-ISEDDAIA---SIHRIFK 192 YHG ++ G N L+PG V+ P P + DD A +I R F+ Sbjct: 150 GYHGTHFGGASVNGNANFRRNYEPLLPG-VFHLAAPYPYRNPFNTDDPAAIAAAIARQFE 208 Query: 193 NDAA---PEDIAAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLIADEVQSGAGRTG 249 ++ A + IAA ++EPV G GG +FM +R +CD HGI+LIADEV + GRTG Sbjct: 209 DEIAFQGADTIAAFIMEPVLGAGGVIVPHESFMPLMREICDRHGILLIADEVITAFGRTG 268 Query: 250 TLFAMEQMGVAPDLTTFAKSIAGG-FPLAGVTGRAEV-------MDAVAPGGLGGTYAGN 301 GV PD+ T AK+I G FP V +V +++ G G TY+G+ Sbjct: 269 AWTGSRGWGVKPDMMTTAKAITNGYFPFGAVMISDKVASVFEANKNSLGAIGHGYTYSGH 328 Query: 302 PIACVAALEVLKVFEQENLLQKANDLGQKLKDGLLAIAEKHPEIGDVRGLGAMIAIELFE 361 P+ AAL LK + N A G +L GL + EKH +GDVRG G M A+EL Sbjct: 329 PVGAAAALATLKETARANTAANAGARGVELIAGLNQLKEKHELVGDVRGKGLMAALELVS 388 Query: 362 DGDHNKPDAK-LTAEIVARARDKGLILLSCGPYYNVLRILVPLTIEDAQIRQGLEIISQC 420 D + AK + ++ A ++G+++ + G NV+ I PL I A + + + + Sbjct: 389 DREKKSAAAKTVVQKVYDVAYEEGVMVRTSGA--NVI-ISPPLVITPADVNRIVSALDAG 445 Query: 421 FDEAK 425 AK Sbjct: 446 LSAAK 450 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: 463 Number of extensions: 23 Number of successful extensions: 4 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: 452 Length adjustment: 32 Effective length of query: 394 Effective length of database: 420 Effective search space: 165480 Effective search space used: 165480 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 Sep 24 2021. The underlying query database was built on Sep 17 2021.
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