Align Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial; Beta-alanine-pyruvate aminotransferase 1; EC 2.6.1.44 (characterized)
to candidate WP_012709243.1 NGR_RS24830 aminotransferase
Query= SwissProt::Q940M2 (476 letters) >NCBI__GCF_000018545.1:WP_012709243.1 Length = 975 Score = 318 bits (814), Expect = 7e-91 Identities = 187/478 (39%), Positives = 274/478 (57%), Gaps = 37/478 (7%) Query: 20 AISLLRTDFSTSPSIADAPPHIPPFVHQPRPYKG-----------------PSADEVLQK 62 A+ +R S + I D PP P HQ ++ P A +L++ Sbjct: 499 ALGFMRVQLSNAAEI-DPPPFARP--HQAEAWRRLCPSPADVLGFDCDAPPPQAAALLER 555 Query: 63 RKKFLGPSLFHYYQKPLNIVEGKMQYLYDESGRRYLDAFAGIVTVSCGHCHPDILNAITE 122 R++ +YY+ P I G ++L+D GR YLD + V GH HP + A+ Sbjct: 556 RQRHFARPQKNYYRNPPEIERGWKEHLFDVEGRAYLDMVNNVTIV--GHGHPRLSAAVGR 613 Query: 123 QSKLLQHATTIYLHHAIGDFAEALAAKMPGNLKVVYFVNSGSEANELAMMMARLYTGSLE 182 Q LL + + + + A+ +F+E +AA P L V+ VNSGSEAN+LA+ +A ++G+ Sbjct: 614 QWSLL-NTNSRFHYAAVAEFSERIAALAPEGLDTVFLVNSGSEANDLAIRLAWAHSGART 672 Query: 183 MISLRNAYHGGSSNTIGLTALNTWKYPLPQGE------IHHVVNPDPYRGVFGSDGSL-- 234 M+SL AYHG T+ A++T PQ +H VV+P+ YRG + GS Sbjct: 673 MLSLLEAYHGW---TVASDAVSTSIADNPQALTTRPDWVHPVVSPNTYRGPYRGQGSTGD 729 Query: 235 YAKDVHDHI-EYGTSGK-VAGFIAETIQGVGGAVELAPGYLKSVYEIVRNAGGVCIADEV 292 Y V + E G+ +AGFI E + G G + L PGYL++VY++VR GG+CIADEV Sbjct: 730 YVGAVTTKLKELDEKGESLAGFICEAVYGNAGGIPLPPGYLEAVYQMVRARGGICIADEV 789 Query: 293 QTGFGRTGSHYWGFQTQDVVPDIVTMAKGIGNGLPLGAVVTTPEIASVLASK-ILFNTFG 351 Q G+GR G H+WGF+ Q VVPD++T+AKG+GNG PLGAV+T EIA L + F++ G Sbjct: 790 QVGYGRLGHHFWGFEEQGVVPDVITVAKGMGNGHPLGAVITRREIADALEKEGYFFSSSG 849 Query: 352 GNPVCSAGGLAVLNVIDKEKRQEHCAEVGSHLIQRLKDVQKRHDIIGDVRGRGLMVGIEL 411 G+PV S GL VL+++ E QE+ VG HL RL+ + +R I+G V G GL +G+E Sbjct: 850 GSPVSSVVGLTVLDILHDEALQENARTVGDHLRDRLQALAQRFPIVGAVHGMGLYLGVEF 909 Query: 412 VSDRKDKTPAKAETSVLFEQLRELGILVGKGGLHGNVFRIKPPMCFTKDDADFLVDAL 469 V DR+ PA ET+ + ++L +LG+++ G H NV +IKPP+C +++ ADF D L Sbjct: 910 VRDRETLEPATEETAAICDRLLDLGVIMQPTGDHLNVLKIKPPLCLSRESADFFADML 967 Lambda K H 0.320 0.138 0.412 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: 1118 Number of extensions: 52 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: 476 Length of database: 975 Length adjustment: 39 Effective length of query: 437 Effective length of database: 936 Effective search space: 409032 Effective search space used: 409032 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: 54 (25.4 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