Align L-tyrosine transporter (characterized)
to candidate PP_5031 PP_5031 proline (histidine) APC transporter
Query= reanno::pseudo5_N2C3_1:AO356_18530 (471 letters) >FitnessBrowser__Putida:PP_5031 Length = 467 Score = 392 bits (1006), Expect = e-113 Identities = 204/463 (44%), Positives = 285/463 (61%), Gaps = 14/463 (3%) Query: 11 LKRGLKNRHIQLIALGGAIGTGLFLGSAGVLKSAGPSMILGYAICGFIAFMIMRQLGEMI 70 LKRGL RHI+ +ALG AIGTGLF GSA ++ AGP+++L Y I G FM+MR LGEM Sbjct: 7 LKRGLSARHIRFMALGSAIGTGLFYGSASAIQMAGPAVLLAYLIGGAAVFMVMRALGEMA 66 Query: 71 VEEPVAGSFSHFAHKYWGGFAGFLSGWNCWILYILVGMSELTAVGKYIHYWAPDIPTWVS 130 V PVAGSF H+A Y G AGF+ GW ++V ++++TA G Y+ +W P++ W+ Sbjct: 67 VHNPVAGSFGHYATTYLGPMAGFILGWTYAFEMVIVAIADVTAFGIYMGFWFPEVARWIW 126 Query: 131 AAAFFILINAINLANVKVFGEAEFWFAIIKVVAIVGMIALGSYLLVSGHG----GPQASV 186 LI +NL NVKVFGE EFW +++KV AIV MI G ++ G G + Sbjct: 127 VLGIVFLIGGLNLCNVKVFGEMEFWLSLLKVGAIVAMILAGLGIMAFGFSQVGTGHAVGM 186 Query: 187 TNLWSHGGFFPNGVSGLVMAMAIIMFSFGGLEMLGFTAAEADKPKTVIPKAINQVIYRIL 246 +NL+ HGGF PNGV GL+ + A++MF+FGG+E++G TA EA P+ VIPKAIN V RIL Sbjct: 187 SNLFDHGGFMPNGVGGLIASFAVVMFAFGGIEIIGVTAGEAKDPQRVIPKAINAVPLRIL 246 Query: 247 IFYIGALVVLLSLTPWDSLLATLNASGDAYSGSPFVQVFSMLGSNTAAHILNFVVLTAAL 306 +FY+ L VL+ L PW + GSPFVQ+FS LG +AA +LN VV++AA+ Sbjct: 247 LFYVLTLFVLMCLYPWPQI---------GSQGSPFVQIFSNLGIGSAAAVLNVVVISAAI 297 Query: 307 SVYNSGTYCNSRMLLGMAEQGDAPKALSRIDKRGVPVRSILASAAVTLVAVLLNYLVPQH 366 S NS + RM+ G+A+QG AP+ S++ K GVP +++ A L+ VLLNYL+P++ Sbjct: 298 SAINSDIFGAGRMMYGLAQQGHAPRGFSKLSKHGVPWMTVVVMGAALLIGVLLNYLIPEN 357 Query: 367 ALELLMSLVVATLVINWAMISYSHFKFRQHMNQTQQTPL-FKALWYPYGNYICLAFVVFI 425 L+ S+ V W MI + R+ M++ Q L F ++PYG + +AF+VFI Sbjct: 358 VFLLIASIATFATVWVWLMILLTQVAMRRSMSREQVAQLKFPVPFWPYGPAMAIAFMVFI 417 Query: 426 LGVMLLIPGIQISVYAIPVWVVFMWVCYVIKNKRSARQELAVA 468 GV+ P Q ++ +WVVF+ Y++ K A Q VA Sbjct: 418 FGVLGYFPDTQAALIVGVIWVVFLVASYLLWCKPRAGQGQPVA 460 Lambda K H 0.327 0.139 0.432 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: 659 Number of extensions: 38 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: 471 Length of database: 467 Length adjustment: 33 Effective length of query: 438 Effective length of database: 434 Effective search space: 190092 Effective search space used: 190092 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