Align MFS transporter (characterized, see rationale)
to candidate GFF4779 PS417_24450 membrane protein
Query= uniprot:A0A166QG26 (467 letters) >lcl|FitnessBrowser__WCS417:GFF4779 PS417_24450 membrane protein Length = 444 Score = 296 bits (759), Expect = 7e-85 Identities = 160/455 (35%), Positives = 242/455 (53%), Gaps = 40/455 (8%) Query: 15 AVGNYRWTICALLFFATTVNYLDRQVLSLLAPDLSTQFGWSNSDYANIASVFQFVYAISM 74 AVG RW + AL+FFATT+NY+DR L ++ P L+ + W+ DYANI FQ YAI Sbjct: 28 AVGKTRWGMLALVFFATTLNYIDRAALGVMQPILAKEMSWTAMDYANINFWFQVGYAIGF 87 Query: 75 LFAGRVVDKIGTKTAYVVAICIWSTGAVMHAFAVPMGEGIGAVSSALGIAMIPVSIAGFM 134 + GR++D++G K + A+ +WS H A S GFM Sbjct: 88 VLQGRLIDRVGVKRVFFCAVLLWSLATGAHGLAT--------------------SAVGFM 127 Query: 135 VSRAVLAIGEAGNFPIAIKATAEYFPKKERSFATGIFNSGANVGAILAPICVPLIASLWG 194 V R +L + EA N+P +K T +FP ER+ ATGIFN+G NVGA++ P+ +PLI +WG Sbjct: 128 VCRFILGLTEAANYPACVKTTRLWFPAGERAVATGIFNAGTNVGAMMTPMLLPLILHVWG 187 Query: 195 WEAAFIVIGMLGFVWVGVWIALYEKPEQQKRLSAQELAYIRSDQVVPVVTRPVPGVADKK 254 W+AAF+ + LG +W+ W Y PE + EL Y+ + P + Sbjct: 188 WQAAFLCMSALGGIWLVFWGLKYFNPEDHPSVKQSELDYVLQE------AEP----EQPR 237 Query: 255 VSWFKLLTYRQTWAFAFGKFMTDGVWWFFLFWLPTYLSAQY--GMKGQAIVMPLAVLYSM 312 V + ++L R TWAFA MT V+WF+L+WLP +L+ QY G+ + +PL ++Y Sbjct: 238 VPFTRILRMRGTWAFALAYSMTAPVFWFYLYWLPPFLNQQYNLGINVTQMGIPLIIIYLT 297 Query: 313 TMIGSIGGGWFPSYFMSRGDAPYDGRMKAMLVIAFFPLLVLLAQPLGYISFWVPVLLIGV 372 GS+GGG S+ + RG R+ +ML+ A + V++A G WV V I + Sbjct: 298 ADFGSVGGGILSSFLIGRGMNSIKARLLSMLLFACCIVGVIMA--AGSSQLWVAVFAISL 355 Query: 373 GASAHQAWSCNIFTTVSDMFPQKSIASVVGIGGLAGGLGGVVMTKIGGWVIDHYKLIGDI 432 AHQAW+ NI++ V D P+ +++V G GG+ +GG+ MT+I G ++ Sbjct: 356 AIGAHQAWTANIWSLVMDYTPKHMMSTVFGFGGMCAAIGGMFMTQIVGHILT------VT 409 Query: 433 HTGYMIMFAICALAYLVAWSVMKALVPRHKEITDL 467 + Y ++F + Y +A + M + PR D+ Sbjct: 410 NNNYTVLFTLIPAMYFIALTWMYFMAPRKIPTVDV 444 Lambda K H 0.327 0.140 0.449 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: 708 Number of extensions: 37 Number of successful extensions: 7 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: 467 Length of database: 444 Length adjustment: 33 Effective length of query: 434 Effective length of database: 411 Effective search space: 178374 Effective search space used: 178374 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