Align Aromatic-amino-acid aminotransferase 1; ARAT-I; AROAT; EC 2.6.1.57 (characterized)
to candidate RR42_RS14595 RR42_RS14595 2-aminoadipate aminotransferase
Query= SwissProt::H3ZPL1 (417 letters) >lcl|FitnessBrowser__Cup4G11:RR42_RS14595 RR42_RS14595 2-aminoadipate aminotransferase Length = 395 Score = 322 bits (826), Expect = 1e-92 Identities = 174/395 (44%), Positives = 249/395 (63%), Gaps = 13/395 (3%) Query: 23 SEKALGMKASEIRELLKLVETSDVISLAGGLPAPETFPVEIIGEITKEVLEKHAAQALQY 82 S +A + +S IRE+LK+ E +VIS AGGLP+P TFPV + + + + ALQY Sbjct: 6 SRRAQQLTSSAIREILKVTERPEVISFAGGLPSPATFPVAAMEQAVARIFADNPQAALQY 65 Query: 83 GTTKGFTPLRLALAEWMRERYDIPISKVDIMTTSGSQQALDLIGRVFINPGDIIVVEAPT 142 T+G+ PLR E++ +R+ + + +V + T+GSQQALDLI +V I+PG ++VE P+ Sbjct: 66 AATEGYMPLR----EFIAKRHAVDVERV--LITTGSQQALDLIAKVMIDPGSPVLVETPS 119 Query: 143 YLAALQAFKYYEPEFVQIPLDDEGMNVDLLEEKLQELEKEGKKVKIVYTIPTFQNPAGVT 202 YL ALQAF +EPEFV +P DD+ LL E L G + +Y +P FQNP G Sbjct: 120 YLGALQAFSLFEPEFVSVPGDDKS----LLPESLTPELTAG--ARFLYALPNFQNPTGRR 173 Query: 203 MNEKRRKRLLELASQYDFIIVEDNPYGELRYSGEPVKPIKAWDEEGRVIYLGTFSKILAP 262 M +RR+ L+ A + ++VED+PYGEL YSG+ + + + + +G VIY+G+FSKILAP Sbjct: 174 MPLERRQALVARARELGLLLVEDDPYGELSYSGDQLPSLLSMNPDG-VIYMGSFSKILAP 232 Query: 263 GFRIGWIAAEPHFIRKLEIAKQSVDLCTNTFSQVIAWKYVEGGYLDKHIPKIIEFYKPRR 322 G R+G++ A P KL AKQ+ DL T +F+Q +A++ V G LD HIP I Y + Sbjct: 233 GLRLGFVIAPPELHFKLCQAKQASDLHTPSFTQRLAYEVVRDGLLDSHIPTIRTLYAAQC 292 Query: 323 DAMLKALEEFMPDGVKWTKPEGGMFVWATLPEGIDTKLMLEKAVAKGVAYVPGEAFFAHR 382 AML +L MP+GV W PEGGMF+W LPEG+D+ +L++AV + VAYVPG F+A Sbjct: 293 QAMLDSLARHMPEGVTWNAPEGGMFIWMELPEGLDSMEILQEAVNRNVAYVPGAPFYASN 352 Query: 383 DVKNTMRLNFTYVPEEKIREGIKRLAETIKEEMKK 417 +N +RL F V E+I +G+ L +E + K Sbjct: 353 PRRNALRLAFVTVAPERIEQGVAILGTLFREAIAK 387 Lambda K H 0.318 0.137 0.398 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: 481 Number of extensions: 20 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 417 Length of database: 395 Length adjustment: 31 Effective length of query: 386 Effective length of database: 364 Effective search space: 140504 Effective search space used: 140504 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 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