Align L-tyrosine transporter (characterized)
to candidate N515DRAFT_2630 N515DRAFT_2630 amino acid/polyamine/organocation transporter, APC superfamily
Query= reanno::pseudo5_N2C3_1:AO356_18530 (471 letters) >FitnessBrowser__Dyella79:N515DRAFT_2630 Length = 454 Score = 417 bits (1073), Expect = e-121 Identities = 205/448 (45%), Positives = 293/448 (65%), Gaps = 12/448 (2%) Query: 11 LKRGLKNRHIQLIALGGAIGTGLFLGSAGVLKSAGPSMILGYAICGFIAFMIMRQLGEMI 70 L+RGL+ RHI+L+ALG AIG GLFLGSA ++ AGP+++L Y + G F+IMR LGEM Sbjct: 7 LQRGLQERHIRLMALGSAIGVGLFLGSANAIRLAGPAILLSYLLGGVAIFIIMRALGEMA 66 Query: 71 VEEPVAGSFSHFAHKYWGGFAGFLSGWNCWILYILVGMSELTAVGKYIHYWAPDIPTWVS 130 V+ PVAGSFS +A Y G G+L+GWN W ++++ ++E+TAVG Y+ W PD+P W+ Sbjct: 67 VQNPVAGSFSRYAQDYLGPLPGYLTGWNYWFMWLMTCIAEITAVGVYMGVWFPDVPQWIW 126 Query: 131 AAAFFILINAINLANVKVFGEAEFWFAIIKVVAIVGMIALGSYLLVSGHG--GPQASVTN 188 A A + + A+NLA VK +GE EFWFA+IKVV IV MI G ++V G G G ++N Sbjct: 127 ALAALVTMGAVNLAAVKAYGEFEFWFAMIKVVTIVLMIVGGGAMIVFGLGNQGVPTGISN 186 Query: 189 LWSHGGFFPNGVSGLVMAMAIIMFSFGGLEMLGFTAAEADKPKTVIPKAINQVIYRILIF 248 LW+HGGF PNG G++MA+ ++MF++ G+EM+G TA EAD PK IP AIN V +RILIF Sbjct: 187 LWTHGGFMPNGAKGMLMALQMVMFAYLGVEMIGLTAGEADNPKKSIPDAINSVFWRILIF 246 Query: 249 YIGALVVLLSLTPWDSLLATLNASGDAYSGSPFVQVFSMLGSNTAAHILNFVVLTAALSV 308 Y+GAL V++S+ PW+ L GSPFV F LG +AA I+NFVVLTAALS Sbjct: 247 YVGALFVIMSIYPWNEL---------GTHGSPFVMTFERLGIKSAAGIINFVVLTAALSS 297 Query: 309 YNSGTYCNSRMLLGMAEQGDAPKALSRIDKRGVPVRSILASAAVTLVAVLLNYLVPQHAL 368 N G Y RML +A+QG AP+ + G+P R++L S L VLLNYLVP Sbjct: 298 CNGGIYSTGRMLFNLAQQGQAPRTFAVTSPSGIPNRAVLVSLVALLFGVLLNYLVPAKVF 357 Query: 369 ELLMSLVVATLVINWAMISYSHFKFRQHMNQTQQTPL-FKALWYPYGNYICLAFVVFILG 427 + S + W ++ + K+R+ +++ Q++ L F+ ++PY +Y+ LAF+V ++G Sbjct: 358 VWVTSAATFGAIWTWGIVLITQMKYRRGLSEAQRSQLVFRMPFFPYASYLALAFLVLVVG 417 Query: 428 VMLLIPGIQISVYAIPVWVVFMWVCYVI 455 +M P ++++ P+W+V + V Y + Sbjct: 418 LMGYFPDTRVALIVGPLWLVLLTVLYYV 445 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: 629 Number of extensions: 30 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: 454 Length adjustment: 33 Effective length of query: 438 Effective length of database: 421 Effective search space: 184398 Effective search space used: 184398 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