Align lysine-specific permease (characterized)
to candidate WP_008805329.1 KVAR_RS20260 S-methylmethionine permease
Query= CharProtDB::CH_003129 (489 letters) >NCBI__GCF_000025465.1:WP_008805329.1 Length = 469 Score = 340 bits (872), Expect = 6e-98 Identities = 185/479 (38%), Positives = 272/479 (56%), Gaps = 22/479 (4%) Query: 7 TTEAPG--LRRELKARHLTMIAIGGSIGTGLFVASGATISQAGPGGALLSYMLIGLMVYF 64 TT+ G L+R +K RHL M+++GG IGTGLF +G IS G G LL+Y++ L+V+ Sbjct: 4 TTQQQGGQLKRTMKTRHLIMLSLGGVIGTGLFFNTGYIISTTGAAGTLLAYLIGALVVWL 63 Query: 65 LMTSLGELAAYMPVSGSFATYGQNYVEEGFGFALGWNYWYNWAVTIAVDLVAAQLVMSWW 124 +M LGEL+ MP +G+F Y Y+ G+ + W YW W V + AA M +W Sbjct: 64 VMQCLGELSVAMPETGAFHVYAARYLGPATGYTVAWLYWLTWTVALGSSFTAAGFCMQYW 123 Query: 125 FPDTPGWIWSALFLGVIFLLNYISVRGFGEAEYWFSLIKVTTVIVFIIVGVLMIIGIF-- 182 FP P WIW +F VIF LN IS R F E E+WFSL+KV T+I FII+G I GI Sbjct: 124 FPQVPVWIWCVVFCAVIFGLNIISTRFFAEGEFWFSLVKVITIIAFIILGGAAIFGIIPM 183 Query: 183 -KGAQPAGWSNWTIGEAPFAGGFAAMIGVAMIVGFSFQGTELIGIAAGESEDPAKNIPRA 241 G+ G N T E F G ++ + V F+F GTELIGIAAGE+E+P K IP A Sbjct: 184 QDGSPAPGLHNIT-AEGWFPHGGLPILMTMVAVNFAFSGTELIGIAAGETENPHKVIPVA 242 Query: 242 VRQVFWRILLFYVFAILIISLIIPYTDPSLLRNDVKDISVSPFTLVFQHAGLLSAAAVMN 301 +R R+++F++ + +++ +IP + SPF LVF+ G+ AA + N Sbjct: 243 IRTTIARLIIFFIGTVFVLAALIPMQQAG--------VEKSPFVLVFEKVGIPYAADIFN 294 Query: 302 AVILTAVLSAGNSGMYASTRMLYTLACDGKAPRIFAKLSRGGVPRNALYATTVIAGLCFL 361 VILTA+LSA NSG+YAS RML++L+ + P FAK+++ GVP AL + + L Sbjct: 295 FVILTAILSAANSGLYASGRMLWSLSNEKTLPACFAKVNKRGVPVTALSVSMLGGVLALF 354 Query: 362 TSMFGNQTVYLWLLNTSGMTGFIAWLGIAISHYRFRRGYVLQGHDINDLPYRSGFFPLGP 421 +S+ TV++ L SG WL I SH+ FRR ++ QG ++DL YR+ ++P+ P Sbjct: 355 SSVVAPDTVFVALSAISGFAVVAVWLSICASHFMFRRRHLQQGKALSDLQYRAPWYPVVP 414 Query: 422 IFAFILCLIITLGQNYEAFLKDTIDWGGVAATYIGIPLFLIIWFGYKLIKGTHFVRYSE 480 + F+LCL+ +G ++ + A + GIP + + + L + + + S+ Sbjct: 415 VLGFVLCLVACVGLAFDPSQR--------IALWCGIPFVALCYGAWYLTRSRNMTQESQ 465 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: 722 Number of extensions: 36 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: 469 Length adjustment: 34 Effective length of query: 455 Effective length of database: 435 Effective search space: 197925 Effective search space used: 197925 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 Apr 09 2024. 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