Align Serine transporter (characterized)
to candidate 7026223 Shewana3_3365 serine transporter, putative (RefSeq)
Query= SwissProt::P0AAD6 (429 letters) >lcl|FitnessBrowser__ANA3:7026223 Shewana3_3365 serine transporter, putative (RefSeq) Length = 430 Score = 473 bits (1218), Expect = e-138 Identities = 238/429 (55%), Positives = 307/429 (71%), Gaps = 7/429 (1%) Query: 1 METTQTSTIASKDSRSAWRKTDTMWMLGLYGTAIGAGVLFLPINAGVGGMIPLIIMAILA 60 +ET Q ST S W + DT WML L+GTA+GAG+LFLPINAG+GG PL++MAI+ Sbjct: 9 LETPQ-STQESTTRHLPWTRQDTTWMLSLFGTAVGAGILFLPINAGMGGFWPLVLMAIII 67 Query: 61 FPMTFFAHRGLTRFVLSGKNPGEDITEVVEEHFGIGAGKLITLLYFFAIYPILLVYSVAI 120 PMT+ AHRGL+RFV S PG DIT+VVEEHFGIGAGK ITLLYF AIYPI+L+Y V I Sbjct: 68 GPMTYLAHRGLSRFVCSSSIPGSDITQVVEEHFGIGAGKAITLLYFLAIYPIVLIYGVGI 127 Query: 121 TNTVESFMSHQLGMTPPPRAILSLILIVGMMTIVRFGEQMIVKAMSILVFPFVGVLMLLA 180 TNTV+SF+ +QLGM PPR +LS +LI GMM ++ GEQ ++K +LV+P VG+L ++ Sbjct: 128 TNTVDSFIVNQLGMASPPRFLLSGVLIFGMMAVMVAGEQFMLKVTQLLVYPLVGILAFMS 187 Query: 181 LYLIPQWNGAALETLSLDTASATGNGLWMTLWLAIPVMVFSFNHSPIISSFAVAKREEYG 240 +YLIP+W AL+ + DT + G T+WL IPV+VF+FNHSP IS F+V+ + ++G Sbjct: 188 IYLIPEWKMDALQVVP-DTGAFLG-----TVWLTIPVLVFAFNHSPAISQFSVSLKRDHG 241 Query: 241 DMAEQKCSKILAFAHIMMVLTVMFFVFSCVLSLTPADLAAAKEQNISILSYLANHFNAPV 300 A +K IL +M+V VM FVFSCVLSL+P LA AK +N+ ILSYLAN ++ Sbjct: 242 VNAARKADVILRNTSMMLVGFVMLFVFSCVLSLSPEQLAEAKAKNLPILSYLANVHDSGF 301 Query: 301 IAWMAPIIAIIAITKSFLGHYLGAREGFNGMVIKSLRGKGKSIEINKLNRITALFMLVTT 360 +++ P IA +AI SF GHY+GA EG G+++K LR K I NKLN+ +FM T Sbjct: 302 VSYFGPFIAFVAIVSSFFGHYMGATEGMKGIIVKQLRSSNKQISENKLNKFILVFMFATI 361 Query: 361 WIVATLNPSILGMIETLGGPIIAMILFLMPMYAIQKVPAMRKYSGHISNVFVVVMGLIAI 420 W VA NPSILGMIE LGGPIIA IL+LMPMYA+ KVPA++ Y ISNVFV++ GL+A+ Sbjct: 362 WAVAIKNPSILGMIEALGGPIIAAILYLMPMYAVYKVPALKAYRNRISNVFVIIAGLLAM 421 Query: 421 SAIFYSLFS 429 +AI + L S Sbjct: 422 TAILFGLLS 430 Lambda K H 0.328 0.140 0.416 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: 581 Number of extensions: 24 Number of successful extensions: 2 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: 429 Length of database: 430 Length adjustment: 32 Effective length of query: 397 Effective length of database: 398 Effective search space: 158006 Effective search space used: 158006 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 (21.8 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