Align Lysine permease LysP (characterized)
to candidate WP_054653911.1 CES79_RS01340 amino acid permease
Query= SwissProt::A2RNZ6 (508 letters) >NCBI__GCF_002217945.1:WP_054653911.1 Length = 491 Score = 605 bits (1560), Expect = e-177 Identities = 296/489 (60%), Positives = 374/489 (76%), Gaps = 8/489 (1%) Query: 21 LENSSNSTTETQVKRALKSRHVSMIALGGTIGTGLFLTSGDVIHTAGPFGALTAYVLIGA 80 + N ++ +VKR+LK+RH+SMIALGG+IGTGLF+ SG I TAGP G L AYV +G Sbjct: 1 MANQTSGNGGNEVKRSLKTRHLSMIALGGSIGTGLFVASGSAISTAGPGGGLLAYVALGI 60 Query: 81 MVYFLMTSLGEMATYLPTSGSFSDYGTRYVDPAFGFALGWNYWLNWAITVAVDLTAVALC 140 MVYFLMTSLGEMAT +P SGSF+ Y T+YVDPA GFA+GWNYW NWAIT+AVD++ AL Sbjct: 61 MVYFLMTSLGEMATNMPVSGSFATYSTKYVDPALGFAMGWNYWFNWAITLAVDISTAALV 120 Query: 141 IKFWLPDVPSWIFSLIALIIVFSINALSVKTFGETEYWLSAIKITVVVLFLIIGFLSIFG 200 +KFWLP+VP WI+S I L+++F INAL+VK FGETEYW++ IK+ VV+FLI+GF +IFG Sbjct: 121 MKFWLPNVPGWIWSTIILVMIFMINALTVKAFGETEYWMAMIKVVTVVIFLIVGFATIFG 180 Query: 201 IMGGHIDVAKNLSVGNHGFVGGLGSFTTGGGILGVLLVAGFSFQGTELLGITAGEAENPE 260 IMGGH N + FVGG+ + IL V +VAGFSFQGTEL+GITAGE+ PE Sbjct: 181 IMGGHATGLSNFTYKKAPFVGGVPA------ILSVFVVAGFSFQGTELVGITAGESATPE 234 Query: 261 KSIPKAMNSIFWRILVFYILSIFVMAAIIPFTDPHLVGGNSA--AQSPFTIVFERVGFSI 318 KS+PKA+N +FWRIL+FYIL+IFV+A +IP+T P L+G +++ A SPFT+VFER G + Sbjct: 235 KSVPKAINQVFWRILLFYILAIFVIACLIPYTSPKLLGSSASDIAISPFTLVFERAGLAA 294 Query: 319 AASIMNAVVLTSVVSAANSGMYASTRMLYSLAKDGGAPKIFSKTSKNGIPFIALLATTAV 378 AAS+MNAV+LTSV+SAANSGMYAS+RMLYSLA D APK F T+KNG+P A +ATT V Sbjct: 295 AASVMNAVILTSVISAANSGMYASSRMLYSLALDDFAPKYFEHTTKNGVPLRAQVATTIV 354 Query: 379 ALLTFLTSIYGVSFFTLLVSASGLTGFIAWIGIAISHFRFRRAYVAQGKDVKKLPYHAKL 438 + F+TSI G ++ L++ASGLTGFIAW+GIAISHFRFRRA+V QG + +L YHAK Sbjct: 355 GAIAFITSIAGPEVYSWLIAASGLTGFIAWVGIAISHFRFRRAFVKQGHQLSELKYHAKW 414 Query: 439 FPFGPILALIMTVLVTLGQDPMLLFGKTWVQGVVMYAAIPLFFILYLGYKFKNKTKLIPL 498 FPFGPILA ++ +LV +GQ+P W Q V Y ++PLFFIL+ YK K T +IPL Sbjct: 415 FPFGPILAFVLCILVIIGQNPSAFVHFDWKQIGVTYLSVPLFFILFFWYKIKYHTGIIPL 474 Query: 499 KDVDLSRHK 507 VD++ HK Sbjct: 475 DKVDVTPHK 483 Lambda K H 0.326 0.141 0.422 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: 710 Number of extensions: 33 Number of successful extensions: 3 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: 508 Length of database: 491 Length adjustment: 34 Effective length of query: 474 Effective length of database: 457 Effective search space: 216618 Effective search space used: 216618 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 24 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:
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