Align Aromatic amino acid permease, AroP (characterized)
to candidate AO356_28340 AO356_28340 GABA permease
Query= TCDB::Q46065 (463 letters) >lcl|FitnessBrowser__pseudo5_N2C3_1:AO356_28340 AO356_28340 GABA permease Length = 466 Score = 357 bits (917), Expect = e-103 Identities = 182/446 (40%), Positives = 274/446 (61%), Gaps = 8/446 (1%) Query: 4 SNEGLGTGLRTRHLTMMGLGSAIGAGLFLGTGVGIRAAGPAVLLAYIIAGAIVVLVMQML 63 SN L G + RH+TM+ + IGAGLF+G+G I AAGPAV+LAY+ +G +VVLVM+ML Sbjct: 9 SNGHLAQGFKPRHVTMLSIAGIIGAGLFVGSGHAIAAAGPAVMLAYLFSGLLVVLVMRML 68 Query: 64 GEMAAARPASGSFSRYGEDAFGHWAGFSLGWLYWFMLIMVMGAEMTGAAAIMGAWF-GVE 122 GEMA A P +GSFS Y + A G WAGF++GWLYW+ ++V+ E A ++ WF V+ Sbjct: 69 GEMAVANPDTGSFSTYADQAIGRWAGFTIGWLYWWFWVLVIPIEALAAGHVLNQWFPAVD 128 Query: 123 PWIPSLVCVVFFAVVNLVAVRGFGEFEYWFAFIKVAVIIAFLIIGIALIFGWLPGSTFVG 182 W+ + V +V AV NL +V +GEFE+WFA KV II F+ +G A++ GW+P G Sbjct: 129 AWLFASVSIVLLAVTNLFSVSKYGEFEFWFAMAKVVAIIGFISLGFAVLMGWIPEREASG 188 Query: 183 TSNFIGDH-GFMPNGISGVAAGLLAVAFAFGGIEIVTIAAAESDKPREAISLAVRAVIWR 241 S + +H GF PNG+S V + + F+F G E VTIAAAESD P + I+ A R+VIWR Sbjct: 189 LSRLMEEHGGFAPNGLSAVVGAFITIMFSFIGTEAVTIAAAESDNPAQNIAKATRSVIWR 248 Query: 242 ISVFYLGSVLVITFLMPYESINGADTAAESPFTQILAMANIPGTVGFMEAIIVLALLSAF 301 I VFYL S+ V+ ++P+ N A+ + + L + NIP ++ ++++A+ S Sbjct: 249 IGVFYLLSIFVVISVVPW---NDPLLASVGSYQRALELMNIPHAKFLVDMVVLIAVASCM 305 Query: 302 NAQIYATSRLVFSMANRQDAPRVFSKLSTSHVPTNAVLLSMFFAFVSVGLQYWNPAGLLD 361 N+ IY SR+++S+ R DAP+ S++ VP +AV+ S Y+ PAGL Sbjct: 306 NSSIYIASRMLYSLGRRGDAPKALKVTSSAGVPRSAVIASTVLGAGVTLFSYFMPAGLFQ 365 Query: 362 FLLNAVGGCLIVVWAMITLSQLKLRKELQANDEISTVRMWAHPWLGILTLVLLAGLVALM 421 FLL + G ++V+ +I +SQL++R+ +Q + RMW PWL L +V ++ +A+M Sbjct: 366 FLLASSGAIALLVYLVIAISQLRMRRMMQRQNIELPFRMWLFPWLTWLVIVFISAALAVM 425 Query: 422 LGDAASRSQVYSVAIVYGFLVLLSFV 447 + RS+ V+ G +++SF+ Sbjct: 426 MITPEHRSE---VSTTLGLALIISFI 448 Lambda K H 0.327 0.140 0.428 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: 581 Number of extensions: 34 Number of successful extensions: 4 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: 463 Length of database: 466 Length adjustment: 33 Effective length of query: 430 Effective length of database: 433 Effective search space: 186190 Effective search space used: 186190 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (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