Align Probable aspartate aminotransferase; AspAT; EC 2.6.1.1; Transaminase A (uncharacterized)
to candidate 7024974 Shewana3_2145 aminotransferase AlaT (RefSeq)
Query= curated2:P63499 (429 letters) >FitnessBrowser__ANA3:7024974 Length = 404 Score = 516 bits (1329), Expect = e-151 Identities = 246/404 (60%), Positives = 314/404 (77%), Gaps = 1/404 (0%) Query: 26 RAFAQSAKLQDVLYEIRGPVHQHAARLEAEGHRILKLNIGNPAPFGFEAPDVIMRDIIQA 85 R +S KL V Y+IRGPVH+ A RLE EGHRILKLNIGNPAPFGFEAP+ I+RD+I Sbjct: 2 RPIIKSNKLDTVCYDIRGPVHKEARRLEDEGHRILKLNIGNPAPFGFEAPEEIVRDVILN 61 Query: 86 LPYAQGYSDSQGILSARRAVVTRYELVPGFPRFDVDDVYLGNGVSELITMTLQALLDNGD 145 LP AQGY +S+G+ SAR+A+V Y+ G D++DVY+GNGVSELI M +Q LL+ D Sbjct: 62 LPSAQGYCESKGLFSARKAIVQHYQ-AQGIKGVDIEDVYIGNGVSELIMMAMQGLLNTDD 120 Query: 146 QVLIPSPDYPLWTASTSLAGGTPVHYLCDETQGWQPDIADLESKITERTKALVVINPNNP 205 +VL+PSPDYPLWTA+ +LAGG VHY CDE W PD+ D++SKI+ RT+ +V+INPNNP Sbjct: 121 EVLLPSPDYPLWTAAANLAGGKAVHYRCDEEADWFPDLDDIKSKISSRTRGIVLINPNNP 180 Query: 206 TGAVYSCEILTQMVDLARKHQLLLLADEIYDKILYDDAKHISLASIAPDMLCLTFNGLSK 265 TGAVYS E+L Q+++L R+H L+L ADEIYDKILYD+AKHI AS++ D+L +TFNGLSK Sbjct: 181 TGAVYSKELLLQVIELCREHNLILFADEIYDKILYDEAKHIPAASLSDDILTVTFNGLSK 240 Query: 266 AYRVAGYRAGWLAITGPKEHASSFIEGIGLLANMRLCPNVPAQHAIQVALGGHQSIEDLV 325 AYR AG+R GW+ ++G + A S+IEG+ +L++MRLC NVP QHAIQ ALGG+QSI +L+ Sbjct: 241 AYRAAGFRVGWMMLSGNLKAAKSYIEGLEMLSSMRLCANVPNQHAIQTALGGYQSINELI 300 Query: 326 LPGGRLLEQRDIAWTKLNEIPGVSCVKPAGALYAFPRLDPEVYDIDDDEQLVLDLLLSEK 385 LP GRL QRD + LN+IPGVS KP GALYAFP+LD + +++ DDE+LVLDLL +K Sbjct: 301 LPSGRLTVQRDTCYELLNQIPGVSVKKPKGALYAFPKLDMKKFNLRDDERLVLDLLRDKK 360 Query: 386 ILVTQGTGFNWPAPDHLRLVTLPWSRDLAAAIERLGNFLVSYRQ 429 IL+ G+ FNWP PDHLR+V LP+ DL A+ GNFL +Y+Q Sbjct: 361 ILLVHGSAFNWPEPDHLRVVFLPYKEDLTKALTEFGNFLETYKQ 404 Lambda K H 0.320 0.138 0.419 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: 547 Number of extensions: 20 Number of successful extensions: 2 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: 429 Length of database: 404 Length adjustment: 31 Effective length of query: 398 Effective length of database: 373 Effective search space: 148454 Effective search space used: 148454 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: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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