Align Ornithine aminotransferase; Orn-AT; Lysine aminotransferase; Lys-AT; EC 2.6.1.13; EC 2.6.1.36 (characterized)
to candidate N515DRAFT_3630 N515DRAFT_3630 4-aminobutyrate aminotransferase
Query= SwissProt::Q5JEW1 (445 letters) >FitnessBrowser__Dyella79:N515DRAFT_3630 Length = 469 Score = 211 bits (538), Expect = 3e-59 Identities = 152/434 (35%), Positives = 228/434 (52%), Gaps = 29/434 (6%) Query: 37 PIVIERGEGIRVYDVDGNVFYDFASGVGVINVGHSHPRVVEAIKKQAEKFTHYSLTDFFY 96 P + G+G +YD G F D +N G+ + R+ + +K Q + + + + + Sbjct: 38 PKIFRHGQGSWMYDTAGVPFLDLQMWYSAVNFGYGNKRLNDTLKAQIDTLPQVA-SQYLH 96 Query: 97 ENAIILAEKLIELAPGD--IERKVVYGNSGAEANEAAMKLVK-YGTGRKQFLAFYHAFHG 153 + I LA+ + A ++ +V + GA+A E ++KLV+ Y G+ AF +HG Sbjct: 97 QTRIELAKTIAVDAQQKFGLKGRVHFNVGGAQAVEDSLKLVRNYKNGKSLMFAFEGGYHG 156 Query: 154 RTQAVLSLTAS-KWVQQDGFFPTMPGVTHIPYPNPYRNTWGIDGYEEPDELTNRVLDFIE 212 RT S+T+S ++ ++ G F IP+P P+R G+ E D + E Sbjct: 157 RTLGASSITSSYRYRRRFGHFGER--AMFIPFPYPFRRPKGMTPEEYSDACVRQFERLFE 214 Query: 213 -EYVFRHVPP---HEIGAIFFEPIQGEGGYVVPPKGFFKALKKFADEYGILLADDEVQMG 268 EY P E A + EPIQG GGYV+PPK FFK LKK D+YGIL+ DE+QMG Sbjct: 215 TEYNGVWDPKVNQAEYAAFYVEPIQGTGGYVIPPKNFFKDLKKVLDKYGILMVVDEIQMG 274 Query: 269 IGRTGKFWAIEHFGVEPDLIQFGKAIGGGL-PLAGVIHRADITFDK---PGRHATTFGGN 324 RTGK W+IEHFGV PD+I FGKA+ GL PL+G+ R ++ + PG +TF N Sbjct: 275 FWRTGKLWSIEHFGVTPDIIVFGKALTNGLNPLSGLWAREEMINPEIFPPGSTHSTFNSN 334 Query: 325 PVAIAAGIEVVEIVKEL--LPHVQEVGDYLHKYLEEFKEKYEVIGDARGLGLAQAVEIVK 382 P+ + G+EV+++ EL +V + G + L++ +++++ IGD GLGLA EI Sbjct: 335 PLGTSLGLEVIKMGYELDYETNVAKKGAHFLDALKDLQKRHKEIGDVDGLGLALRAEIC- 393 Query: 383 SKETKEKYPELRDRIV---------KESAKRGLVL--LGCGDNSIRFIPPLIVTKEEIDV 431 + + L DR+V K GLVL G N I F P L +T EEID+ Sbjct: 394 TDDGFTPNKALLDRMVDIGLAGDLEHNGKKIGLVLDVGGWYKNVITFAPSLDITHEEIDL 453 Query: 432 AMEIFEEALKAALK 445 A+ + ++ L A K Sbjct: 454 AIALLDQLLTKAKK 467 Lambda K H 0.320 0.141 0.418 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: 603 Number of extensions: 37 Number of successful extensions: 6 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: 445 Length of database: 469 Length adjustment: 33 Effective length of query: 412 Effective length of database: 436 Effective search space: 179632 Effective search space used: 179632 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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