Align lysine-specific permease (characterized)
to candidate PP_3727 PP_3727 Amino-acid permease RocE
Query= CharProtDB::CH_003129 (489 letters) >FitnessBrowser__Putida:PP_3727 Length = 468 Score = 397 bits (1019), Expect = e-115 Identities = 196/446 (43%), Positives = 288/446 (64%), Gaps = 10/446 (2%) Query: 5 TKTTEAPGLRRELKARHLTMIAIGGSIGTGLFVASGATISQAGPGGALLSYMLIGLMVYF 64 T + E L R LK+RH+ M+++GG IGTGLF+ SG TI+Q GP GA+L+Y++ GL++Y Sbjct: 2 TDSVEKIQLTRALKSRHIFMLSLGGVIGTGLFMGSGVTINQGGPVGAILAYLVAGLLMYL 61 Query: 65 LMTSLGELAAYMPVSGSFATYGQNYVEEGFGFALGWNYWYNWAVTIAVDLVAAQLVMSWW 124 +M LGEL+ MPVSGSF + Y+ GF +GW YW +WA T+ ++ AA ++M+ W Sbjct: 62 VMVCLGELSVQMPVSGSFQAHATKYIGPATGFMIGWVYWMSWATTVGLEFTAAGMLMTRW 121 Query: 125 FPDTPGWIWSALFLGVIFLLNYISVRGFGEAEYWFSLIKVTTVIVFIIVGVLMIIGI--F 182 FP+ P W WSALF+ V+F LN ++ R FGEAEYWFS IKV T++ FI++G+L+I G Sbjct: 122 FPEVPIWYWSALFVVVLFGLNALATRAFGEAEYWFSGIKVATILGFIVIGLLVIFGAIPL 181 Query: 183 KGAQPAGWSNWTIGEAPFAGGFAAMIGVAMIVGFSFQGTELIGIAAGESEDPAKNIPRAV 242 PA N +GE+ F G +A+ V M V ++FQG E++G+AAGE+E P K+IPRAV Sbjct: 182 SSGAPAPMLNNLVGESLFPHGLSAVFAVMMTVVYAFQGCEIMGVAAGETEHPEKSIPRAV 241 Query: 243 RQVFWRILLFYVFAILIISLIIPYTDPSLLRNDVKDISVSPFTLVFQHAGLLSAAAVMNA 302 R V +R+L+FYV AI ++S I+P+ L+ SPF VF G+ AA +MN Sbjct: 242 RNVVFRVLIFYVLAIAVLSAIVPHEQAGLME--------SPFVQVFDMVGIPYAADLMNF 293 Query: 303 VILTAVLSAGNSGMYASTRMLYTLACDGKAPRIFAKLSRGGVPRNALYATTVIAGLCFLT 362 VILTA+LS GNSG+YASTR+L+ ++ G AP+ + LS+ GVP AL T A + +T Sbjct: 294 VILTAILSVGNSGLYASTRILWAMSKTGMAPKSLSPLSKRGVPLRALSITLCFALISLMT 353 Query: 363 SMFGNQTVYLWLLNTSGMTGFIAWLGIAISHYRFRRGYVLQGHDINDLPYRSGFFPLGPI 422 S T+++ L+ SGM+G + W+ IA++ YRFR+ ++ G + DL Y++ +PL P+ Sbjct: 354 SFVAADTLFMVLMAVSGMSGTVTWIVIALAQYRFRKAWLRDGGQLQDLKYKAPLYPLVPL 413 Query: 423 FAFILCLIITLGQNYEAFLKDTIDWG 448 LC + + + + ++ WG Sbjct: 414 LCITLCSSLFVFLALDETQRPSLYWG 439 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: 768 Number of extensions: 38 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: 468 Length adjustment: 34 Effective length of query: 455 Effective length of database: 434 Effective search space: 197470 Effective search space used: 197470 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