Align [LysW]-aminoadipate semialdehyde transaminase; EC 2.6.1.- (uncharacterized)
to candidate AO353_28215 AO353_28215 4-aminobutyrate aminotransferase
Query= curated2:Q5SHH5 (395 letters) >FitnessBrowser__pseudo3_N2E3:AO353_28215 Length = 430 Score = 231 bits (588), Expect = 4e-65 Identities = 155/426 (36%), Positives = 224/426 (52%), Gaps = 31/426 (7%) Query: 1 METRTLEDWRALLEAEKTLDSGVYNKHDLLIVRGQGARVWDAEGNEYIDCVGGYGVANLG 60 M ++ E L + ++ + G+ H L+I R QGA +WD +G Y+D VGG GV N+G Sbjct: 1 MNSKVDETPHLLRQRDQFVPRGLVTAHPLVIDRAQGAELWDVDGKRYLDFVGGIGVLNIG 60 Query: 61 HGNPEVVEAVKRQAETLM--AMPQTLPTPMRGEFYRTLTAILPPELNRVFPVNSGTEANE 118 H +P+VV AV+ Q + + P R I E + SG EA E Sbjct: 61 HNHPKVVAAVQAQLQKVSHACFQVVAYKPYLDLAQRLCEMIGGNEAYKAAFFTSGAEAVE 120 Query: 119 AALKFARAHTGRKKFVAAMRGFSGRTMGSLSVT-WEPKYREPFLPLVEPVEFIPYNDV-- 175 A+K ARAHT R +A GF GRT+ ++T Y++ F P V PY + Sbjct: 121 NAVKIARAHTNRSAVIAFRGGFHGRTLLGTTLTGMSQPYKQNFGPFAPEVFHTPYPNAYR 180 Query: 176 ----EALKRAVDE---------ETAAVILEPVQGEGGVRPATPEFLRAAREITQEKGALL 222 E +A+DE AA+I+EPVQG+GG A EFL+A R +T++ G +L Sbjct: 181 GVSSEMALKALDELLATQVAPERVAAIIIEPVQGDGGFLSAPAEFLQALRALTEKHGIVL 240 Query: 223 ILDEIQTGMGRTGKRFAFEHFGIVPDILTLAKALGGGVPLGAAVMREEVARSMPKGGHGT 282 ILDEIQTG GRTGK F F+H GI PD++T+AK+L GG+PL V + + + GG G Sbjct: 241 ILDEIQTGFGRTGKWFGFQHAGIQPDLVTVAKSLAGGLPLSGVVGKAGIMDAPLPGGLGG 300 Query: 283 TFGGNPLAMAAGVAAIRYLERTRLWERAAELGPWFMEKLRAIPS--PKIREVRGMGLMVG 340 T+GGN L+ AA +A I E+ +L R LG + L + + +I +VRG G M+ Sbjct: 301 TYGGNALSCAAALAVIDAYEQEQLLARGDALGERLRQGLLRLQARHRQIGDVRGSGFMLA 360 Query: 341 LEL------KEKAAPYIARLEKEHR---VLALQAG--PTVIRFLPPLVIEKEDLERVVEA 389 +EL + A RL E R +L ++ G V+RFL PLV ++ ++ ++ Sbjct: 361 IELIKDDDARTPDADLNQRLIDEARAGGLLVIKCGVYRNVLRFLAPLVTTEDQIDEALQI 420 Query: 390 VRAVLA 395 + A LA Sbjct: 421 LEAALA 426 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: 420 Number of extensions: 21 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: 430 Length adjustment: 31 Effective length of query: 364 Effective length of database: 399 Effective search space: 145236 Effective search space used: 145236 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