Align Probable inositol transporter 2 (characterized)
to candidate WP_010536987.1 KCY_RS0109365 sugar porter family MFS transporter
Query= SwissProt::Q9C757 (580 letters) >NCBI__GCF_000226135.1:WP_010536987.1 Length = 460 Score = 178 bits (451), Expect = 5e-49 Identities = 116/354 (32%), Positives = 186/354 (52%), Gaps = 29/354 (8%) Query: 22 TWKNPYVLRLAFSAGIGGLLFGYDTGVISGALLYIRDDFKSVDRNTWLQEMIVSMAVAGA 81 ++ +V + + +GGLLFGYD VI GA + F D T +Q + +S+A+ G Sbjct: 3 SYNKKFVYSICLVSAMGGLLFGYDWVVIGGAKPFYELYFDIADSPT-MQGLAMSVALLGC 61 Query: 82 IVGAAIGGWANDKLGRRSAILMADFLFLLGAIIMAAAPNPSLLVVGRVFVGLGVGMASMT 141 ++GA + G D+ GR+ +L++ F+FL A A S +V R G+G+G+AS Sbjct: 62 LIGAMVAGMMADRYGRKPLLLISAFIFLSSAYATGAFSVFSWFLVARFLGGIGIGIASGL 121 Query: 142 APLYISEASPAKIRGALVSTNGFLIT----GGQFLSYLI------NLAFTDVTGT----- 186 +P+YI+E +P IRG LVS N I G Q ++LI + D+ + Sbjct: 122 SPMYIAEVAPTSIRGKLVSLNQLTIVLGILGAQIANWLIAEPIPADFTPADICASWNGQM 181 Query: 187 -WRWMLGIAGIPALLQFVLMFTLPESPRWLYRKGREEEAKAILRRIYSAEDVEQEIRALK 245 WRWM A PA + +L +PESPRWL KG+ E A +L +I EQE++ ++ Sbjct: 182 GWRWMFWGAAFPAAVFLLLACFIPESPRWLAMKGKRERAWNVLSKIGGNHYAEQELQMVE 241 Query: 246 DSVETEILEEGSSEKINMIKLCKAKTVRRGLIAGVGLQVFQQFVGINTVMYYSPTIVQLA 305 + GSS+ +KL ++ R+ L+ G+ + VFQQ+ G N + Y+ I Q A Sbjct: 242 --------QTGSSKSEGGLKLLFSRPFRKVLVLGIIVAVFQQWCGTNVIFNYAQEIFQSA 293 Query: 306 GFASNRTALLLSLVTAGLNAFGSIISIYFIDRIGRKKLLII---SLFGVIISLG 356 G+ S L +VT N + ++IY ++R+GR+ L+++ L G+ + LG Sbjct: 294 GY-SLGDVLFNIVVTGVANVIFTFVAIYTVERLGRRVLMLLGAGGLAGIYLVLG 346 Score = 67.8 bits (164), Expect = 9e-16 Identities = 32/104 (30%), Positives = 58/104 (55%) Query: 453 GWFALLGLGLYIIFFSPGMGTVPWIVNSEIYPLRFRGICGGIAATANWISNLIVAQSFLS 512 G+F ++ + L I ++ +G + W++ +EI+P R RG+ A W+ + + +F Sbjct: 355 GFFMVVLVVLAIACYAMSLGPITWVLLAEIFPNRVRGVAMATCTFALWVGSFTLTYTFPL 414 Query: 513 LTEAIGTSWTFLIFGVISVIALLFVMVCVPETKGMPMEEIEKML 556 L A+G+ TF I+ I ++ +F +PETKG +E +EK L Sbjct: 415 LNSALGSYGTFWIYSAICLVGFVFFRRALPETKGKSLETLEKDL 458 Lambda K H 0.324 0.139 0.425 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: 697 Number of extensions: 48 Number of successful extensions: 8 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 4 Number of HSP's successfully gapped: 2 Length of query: 580 Length of database: 460 Length adjustment: 35 Effective length of query: 545 Effective length of database: 425 Effective search space: 231625 Effective search space used: 231625 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.5 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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:
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