Align Probable 4-aminobutyrate aminotransferase; EC 2.6.1.19; (S)-3-amino-2-methylpropionate transaminase; EC 2.6.1.22; GABA aminotransferase; GABA-AT; Gamma-amino-N-butyrate transaminase; GABA transaminase; Glutamate:succinic semialdehyde transaminase; L-AIBAT (uncharacterized)
to candidate WP_111607943.1 DK187_RS13845 diaminobutyrate--2-oxoglutarate transaminase
Query= curated2:P94427 (436 letters) >NCBI__GCF_003259225.1:WP_111607943.1 Length = 437 Score = 182 bits (463), Expect = 1e-50 Identities = 133/414 (32%), Positives = 212/414 (51%), Gaps = 37/414 (8%) Query: 35 KGEGAELYDLDGRRFIDFAGAIGTLNVGHSHP----KVVEAVKRQAEELIHPGFNVMMYP 90 + +GA L+D +G +++DF GTLN GH++P K+VE + E+ I G ++ Sbjct: 24 RAQGAYLFDQEGNKYLDFLAGAGTLNYGHNNPIFKEKLVEYI---LEDGITHGLDMHTKA 80 Query: 91 T--YIELAEKLCGIAPGSHEKKAIFLN-SGAEAVENAVKIARKYTKRQGVVSFTRGFHGR 147 ++E+ +K + P E F +G AVE A+K+AR T R+ ++SFT GFHG Sbjct: 81 KGEFLEVFKKHI-LEPRGLEYMVQFTGPTGTNAVEAALKLARNVTGRENIISFTNGFHGC 139 Query: 148 TNMTMSMTSKVKPYKFGFGPFAPEVYQAPFPYYYQKPAGMSDESYDDMVIQAFNDFFIAS 207 + +S+T V PF Y G+ Y D V+ +S Sbjct: 140 SLGALSVTGNSHHRGAAGTSLGAGVSTVPFDGYLGD--GIETTEYLDKVLSD------SS 191 Query: 208 VAPETVACVVMEPVQGEGGFIIPSKRFVQHVASFCKEHGIVFVADEIQTGFARTGTYFAI 267 +T A V++E VQGEGG S ++Q++ + CK+HG++ + D+IQ G RTGT+F+ Sbjct: 192 SGVDTPAAVIVETVQGEGGINAASFGWLQNLEAVCKKHGVLLIVDDIQAGCGRTGTFFSF 251 Query: 268 EHFDVVPDLITVSKSLAA-GLPLSGVIGRAEMLDAAAPGELGGTYAGSPLG-CAAALAVL 325 E + PD++T+SKSL+ GLP + V+ R E LD PGE GT+ G+ L A +A+ Sbjct: 252 EDAGIKPDIVTMSKSLSGYGLPFAVVLMRPE-LDEWKPGEHNGTFRGNNLAFVTAKVAIE 310 Query: 326 DIIEEEGLNERSEEIGKIIEDKAYEWKQEFPFIGD----IRRLGAMAAIEIVKDPDTREP 381 +++ + + G+ I ++ EF G+ ++ G M I V Sbjct: 311 TYWKDDAFEKEIKRKGEYIHERTQAIVNEF---GEGNFTLQGRGMMRGINCVSG------ 361 Query: 382 DKTKAAAIAAYANQNGLLLLTAGINGNIIRFLTPLVISDSLLNEGLSILEAGLR 435 A I QNGL++ T+G + +++FL PL+ISD L +G+ ILE +R Sbjct: 362 --ELAGKITKKCFQNGLMIETSGADDQVVKFLCPLIISDEDLKQGIDILERAIR 413 Lambda K H 0.319 0.136 0.393 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: 475 Number of extensions: 28 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: 436 Length of database: 437 Length adjustment: 32 Effective length of query: 404 Effective length of database: 405 Effective search space: 163620 Effective search space used: 163620 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 (21.7 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