Align [LysW]-aminoadipate semialdehyde transaminase; EC 2.6.1.- (uncharacterized)
to candidate 7023380 Shewana3_0610 bifunctional N-succinyldiaminopimelate-aminotransferase/acetylornithine transaminase protein (RefSeq)
Query= curated2:Q5SHH5 (395 letters) >lcl|FitnessBrowser__ANA3:7023380 Shewana3_0610 bifunctional N-succinyldiaminopimelate- aminotransferase/acetylornithine transaminase protein (RefSeq) Length = 405 Score = 250 bits (638), Expect = 6e-71 Identities = 152/380 (40%), Positives = 213/380 (56%), Gaps = 22/380 (5%) Query: 32 VRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQAETLMAMPQTLPTPMRGE 91 VRG+G+RVWD EGNE+ID GG V LGH +P +V A+K Q E L + + E Sbjct: 28 VRGEGSRVWDQEGNEFIDFAGGIAVNCLGHCHPALVNALKTQGEKLWHLSNVMTNEPALE 87 Query: 92 FYRTLTAILPPELNRVFPVNSGTEANEAALKFARAHTGRK------KFVAAMRGFSGRTM 145 L E RV+ NSG EANEAALK AR + K + +A + F GRT Sbjct: 88 LATKLVNSTFAE--RVYFANSGAEANEAALKLARRYALEKFGVEKDEIIAFDKAFHGRTF 145 Query: 146 GSLSVTWEPKYREPFLPLVEPVEFIPYNDVEALKRAVDEETAAVILEPVQGEGGVRPATP 205 ++SV + Y + F P + + +PYNDV AL+ AV ++T A++LEP+QGEGG+ A P Sbjct: 146 FTVSVGGQAAYSDGFGPKPQSITHLPYNDVAALEAAVSDKTCAIMLEPLQGEGGIIDADP 205 Query: 206 EFLRAAREITQEKGALLILDEIQTGMGRTGKRFAFEHFGIVPDILTLAKALGGGVPLGAA 265 FL+A RE+ + AL+I DE+QTG+GRTG+ +A+ IVPDILT AKALGGG P+ A Sbjct: 206 AFLKAVRELANKHNALVIFDEVQTGVGRTGELYAYMGTDIVPDILTTAKALGGGFPIAAM 265 Query: 266 VMREEVARSMPKGGHGTTFGGNPLAMAAGVAAIRYLERTRLWERAAELGPWFMEKLRAIP 325 + E+A + G HG+T+GGNPLA A G A + + + + L I Sbjct: 266 LTTAEIAEHLKVGTHGSTYGGNPLACAIGNAVLDVVNTPEVLNGVKHREQLLRDGLNKIN 325 Query: 326 SP--KIREVRGMGLMVGLELKE----KAAPYIARLEKEHRVLALQAGPTVIRFLPPLVIE 379 E+RG GL++G L E ++ ++ E +++L AG V+RF P LVI Sbjct: 326 EKYHVFSEIRGKGLLLGAVLNEQYQGRSRDFLVASVAE-GLMSLMAGANVVRFAPSLVIP 384 Query: 380 KEDL-------ERVVEAVRA 392 + D+ ER V ++ A Sbjct: 385 EADIAEGLARFERAVASIAA 404 Lambda K H 0.319 0.137 0.402 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: 396 Number of extensions: 20 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: 395 Length of database: 405 Length adjustment: 31 Effective length of query: 364 Effective length of database: 374 Effective search space: 136136 Effective search space used: 136136 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: 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