Align lysine-specific permease (characterized)
to candidate WP_017178492.1 A1QA_RS0108530 amino acid permease
Query= CharProtDB::CH_003129 (489 letters) >NCBI__GCF_000295095.1:WP_017178492.1 Length = 493 Score = 539 bits (1389), Expect = e-158 Identities = 261/470 (55%), Positives = 342/470 (72%), Gaps = 2/470 (0%) Query: 1 MVSETKTTEAPGLRRELKARHLTMIAIGGSIGTGLFVASGATISQAGPGGALLSYMLIGL 60 + ++ + +E LRR L +RHLTMI+IGG+IGTGLFVASGATISQAGPGGAL++Y +G+ Sbjct: 10 VAADGEQSEPQELRRSLLSRHLTMISIGGAIGTGLFVASGATISQAGPGGALVAYAAVGI 69 Query: 61 MVYFLMTSLGELAAYMPVSGSFATYGQNYVEEGFGFALGWNYWYNWAVTIAVDLVAAQLV 120 MV+ +M SLGE+AAY+PV+GSF YG +V FGFA+GWNYW+NWA+T+A +LVAA LV Sbjct: 70 MVWLIMQSLGEMAAYLPVAGSFGEYGTRFVSPSFGFAIGWNYWFNWAITVAAELVAAALV 129 Query: 121 MSWWFPDTPGWIWSALFLGVIFLLNYISVRGFGEAEYWFSLIKVTTVIVFIIVGVLMIIG 180 M +W PD P +WSALFL ++F +N +S R +GE+E+ F+ IKV VIVF+I+GV MI G Sbjct: 130 MKYWLPDVPSLVWSALFLVILFTINALSARAYGESEFLFASIKVVAVIVFLILGVAMIAG 189 Query: 181 IFKGAQPAGWSNWTIGEAPFAGGFAAMIGVAMIVGFSFQGTELIGIAAGESEDPAKNIPR 240 I G P G NWT GEAPF GG ++ V ++ G+SFQGTELIG AAGE+E+P + IPR Sbjct: 190 ILGGPSP-GTENWTTGEAPFVGGGEGILLVLLVAGYSFQGTELIGTAAGEAENPERTIPR 248 Query: 241 AVRQVFWRILLFYVFAILIISLIIPYTDPSLLRNDVKDISVSPFTLVFQHAGLLSAAAVM 300 A+R +FWRILLFY+ AI +I +IPYTDP+LL + ++SVSPFTLVF+ AG+L AA+V+ Sbjct: 249 AIRTIFWRILLFYIGAIAVIGFLIPYTDPNLLNSAEDNVSVSPFTLVFERAGILGAASVI 308 Query: 301 NAVILTAVLSAGNSGMYASTRMLYTLACDGKAPRIFAKLSRGGVPRNALYATTVIAGLCF 360 NA+ILT+VLSAG SG+Y+STRML+ LA G APR +LS VP NAL ATT++ F Sbjct: 309 NAIILTSVLSAGTSGLYSSTRMLFALAERGHAPRFLTRLSSHQVPMNALVATTLVGLAGF 368 Query: 361 LTSMFGNQTVYLWLLNTSGMTGFIAWLGIAISHYRFRRGYVLQGHDINDLPYRSGFFPLG 420 +TS+ G+ Y +LL S + GFI W GI+ H+RFR QG + DLPYR+ FFP G Sbjct: 369 ITSLVGDGAAYEFLLTLSALAGFITWAGISWCHWRFRMALKAQGQPLTDLPYRARFFPAG 428 Query: 421 PIFAFILCLIITLGQNYEAFLKDTIDWGGVAATYIGIPLFLIIWFGYKLI 470 I A I C+ I +GQ Y G + YIGIP+FL +W+G+KL+ Sbjct: 429 AIVALIACIAIIIGQAYGPVTSGK-SLGEILMPYIGIPVFLALWWGHKLV 477 Lambda K H 0.327 0.142 0.451 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: 877 Number of extensions: 48 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: 489 Length of database: 493 Length adjustment: 34 Effective length of query: 455 Effective length of database: 459 Effective search space: 208845 Effective search space used: 208845 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