Align Lysine/arginine permease CAN1; Basic amino acids permease CAN1 (characterized)
to candidate PP_4495 PP_4495 aromatic amino acid transport protein
Query= SwissProt::A0A1D8PPI5 (571 letters) >FitnessBrowser__Putida:PP_4495 Length = 472 Score = 233 bits (593), Expect = 2e-65 Identities = 138/440 (31%), Positives = 229/440 (52%), Gaps = 20/440 (4%) Query: 51 SSINDEFGEVKRDLKARHVSMIAIGGTIGTGLFISTGSLLHTTGPVMSLISFLFVTTICF 110 S N GE+KR LK RH+ +IA+GG IGTGLF+ + ++ + GP M ++ + I F Sbjct: 2 SGQNMHSGELKRGLKNRHIQLIALGGAIGTGLFLGSAGVMKSAGPSM-ILGYAICGFIAF 60 Query: 111 SVTQSLGEMATYIPISGSFAQFVTRWVSKSCGAANGWLYWFSWAVTFGLELSVVGQVIQF 170 + + LGEM P++GSF+ F + G +GW W + + ELS VG+ + + Sbjct: 61 MIMRQLGEMIVEEPVAGSFSHFAHTYWGGFAGFLSGWNCWVLYILVGMSELSAVGKYVHY 120 Query: 171 WTDAVPLAAWISIFFVILTIFNFFPVKFYGEVEFWIASIKIIAVFGWI-IYAFIMVCGAG 229 W +P + FFV++ N VKF+GE EFW A IK++A+ I + A+++ G+G Sbjct: 121 WWPEIPTWVTAAAFFVLINAINLMNVKFFGEAEFWFAIIKVVAIVSMIGLGAYLLTSGSG 180 Query: 230 KTGPVGFRYWRNGYAWGDGILVNNNGKYVAAFVSGLINSIFTFQGTELVAVTAGEAS--P 287 W +G + +G V+ V L +F+F G E++ TA EA Sbjct: 181 GPEATVANLWTHGGFFPNG---------VSGLVMALAFIMFSFGGLEMLGFTAAEADKPK 231 Query: 288 RALRSAIRKVMFRILVFYVLCMLFMGLLVPYND--PKLTQDGGFTRNSPFLIAMENSGTK 345 + AI +V++RIL+FYV ++ + L P+++ + GG +SPF+ G+ Sbjct: 232 TVIPKAINQVIYRILIFYVGALVVLLSLTPWDNLVASIDASGGSYGSSPFVQVFSLLGSD 291 Query: 346 VLPHIFNAVIVTTIISAGNSNIYSGSRILYGLAQAGVAPKFFLRTNKGGVPFFAVAFTAA 405 V ++ N V++T +S NS Y +R+L G+A+ G AP + +K GVP ++ +AA Sbjct: 292 VAANLLNFVVLTAALSVYNSGTYCNARMLLGMAEQGDAPASLAKVDKRGVPVRSILVSAA 351 Query: 406 FGALGYLACSSQGNKAFTWLLNITATAGLISWGFISVSHIRFMKTLQRRGISRDTLPFKA 465 + L A L+++ +I+W IS SH++F + L R G FKA Sbjct: 352 VTFVAVLLNYLMPQNALELLMSLVVATLVINWAMISYSHLKFRQHLDRTG---QKPLFKA 408 Query: 466 FFMPFSAYYGMVVCFIVVLI 485 + P+ Y +V+ F+V+++ Sbjct: 409 LWYPYGNY--VVLAFVVLIL 426 Lambda K H 0.327 0.140 0.445 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: 699 Number of extensions: 44 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: 571 Length of database: 472 Length adjustment: 35 Effective length of query: 536 Effective length of database: 437 Effective search space: 234232 Effective search space used: 234232 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: 52 (24.6 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