Align The acetate/monochloroacetate (haloacid) permease, Deh4p (Km = 5.5 mμM for acetate; 9 mμM for monochloroacetate) (characterized)
to candidate WP_050654884.1 C1M55_RS10635 MHS family MFS transporter
Query= TCDB::Q7X4L6 (552 letters) >NCBI__GCF_002893965.1:WP_050654884.1 Length = 458 Score = 214 bits (545), Expect = 6e-60 Identities = 115/329 (34%), Positives = 183/329 (55%), Gaps = 6/329 (1%) Query: 5 EGRAAPAPITSEERRVIFASSLGTVFEWYDFYLAGSLAIYI-SRTFF-SGVNPAAGFVFT 62 E +A P+ + ++V+ AS GTV EWY+F+L G+ A + S+ FF G N + Sbjct: 10 ESQAPPSGL----KKVVGASMAGTVVEWYEFFLYGTAATLVFSKVFFPGGGNELDAIIAA 65 Query: 63 LLGFAAGFAVRPFGAIVFGRLGDMIGRKYTFLATILLMGLSTFVVGLLPGYGTIGMTAPV 122 + +A GFA RP G IVFG GD GRK ++LL+G +TF++G LP YG IG AP Sbjct: 66 FITYAVGFAARPLGGIVFGFFGDKFGRKQLLQFSLLLVGAATFLMGCLPTYGQIGYWAPA 125 Query: 123 VFIAMRMLQGLALGGEYGGAATYVAEHAPSNKRGAWTAWIQTTATLGLFISLLVILSVRS 182 + + +R +QG A+GGE+GGA VAEH+P+ RG W++W Q +G ++ +V+L + S Sbjct: 126 LLVTLRFIQGFAVGGEWGGAVLLVAEHSPNRSRGFWSSWPQAGVPMGNLVATVVLLILTS 185 Query: 183 LLNEDTFAAWGWRVPFLVSIVLLAVSVWIRMQLHESPVFERIKAEGKTSKAPLSEAFGQW 242 L++++F +WGWRV F +S V++ V ++R ++ ++P+F + E + KA F Sbjct: 186 TLSDESFMSWGWRVAFWLSAVIVLVGYYVRTKVTDAPIFIAAQKEAELVKATSYSVFEVV 245 Query: 243 KNLKIVLLALFGLTAGQAVVWYTGQFYTLFFLTQTLKVDGTSANMLVAVALLIGTPFFLF 302 K +L GL + V++Y +++ +L + D + +A + Sbjct: 246 KRYPRGVLTAMGLRFAENVMYYLVVTFSITYLKVVVHADTAHILWWMLMAHAVHFAVIPL 305 Query: 303 FGSLSDKIGRKPIIMAGCLIAALTYFPLF 331 G LSD IGR+P+ M G + A F F Sbjct: 306 VGKLSDTIGRRPVYMIGAVTAGTWGFFAF 334 Score = 47.8 bits (112), Expect = 9e-10 Identities = 28/108 (25%), Positives = 57/108 (52%), Gaps = 4/108 (3%) Query: 448 LINWPMSILILTILVL---YVTMVYGPLAAMLVEMFPARIRYTSMSLPYHIGNGWFGGFL 504 ++N + +IL+ +++ + +Y A++ EMFP R+RY+ +SL Y + + G Sbjct: 336 MMNSGHNAVILSAIIIGLVFHAFMYAGQPAIMAEMFPTRMRYSGVSLGYQVTSIVAGSLA 395 Query: 505 PATAFAIIAARGNIYSGLWYPIVIASVAFVIGTLFVKETKGSSTYDAD 552 P A +++ + Y +++AS+ ++ +F +ETKG S D Sbjct: 396 PIIATGLLSKFDSSVPIAIY-LLLASLVTIVAVVFARETKGISLESVD 442 Lambda K H 0.325 0.139 0.420 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: 572 Number of extensions: 27 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 552 Length of database: 458 Length adjustment: 34 Effective length of query: 518 Effective length of database: 424 Effective search space: 219632 Effective search space used: 219632 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 (21.6 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