Align Sucrose permease; Sucrose transport protein (characterized)
to candidate BWI76_RS23415 BWI76_RS23415 MFS transporter
Query= SwissProt::P30000 (415 letters) >FitnessBrowser__Koxy:BWI76_RS23415 Length = 413 Score = 309 bits (792), Expect = 9e-89 Identities = 162/408 (39%), Positives = 248/408 (60%), Gaps = 8/408 (1%) Query: 12 YRFASSYSFLFFISWSLWWSLYAIWLKGHLGLTGTELGTLYSVNQFTSILFMMFYGIVQD 71 Y S+ F FF++WS SL +IWL +GL + G ++SV +++ + YG +QD Sbjct: 10 YPLLSALLFFFFVTWSSSGSLLSIWLHQEVGLKPGDTGIIFSVLSVSALFAQVCYGFIQD 69 Query: 72 KLGLKKPLIWCMSFILVLTGP-FMIYVYEPLLQSNFSVGLILGALFFGLGYLAGCGLLDS 130 KLGL+K L+W ++ +L+L+GP +M++ Y LL+ N +G I G ++ GL + G G+L+S Sbjct: 70 KLGLRKNLLWYITVLLILSGPAYMLFGY--LLKINVLLGSIFGGIYIGLTFNGGIGVLES 127 Query: 131 FTEKMARNFHFEYGTARAWGSFGYAIGAFFAGIFFSISPHINFWLVSLFGAVFMMI--NM 188 +TE++AR FE+G AR WGS G+A+ FFAG+ F+I+PH+NF + S G VF ++ + Sbjct: 128 YTERVARQSQFEFGKARMWGSLGWAVATFFAGLLFNINPHLNFAVASCSGLVFFILLARL 187 Query: 189 RFKDKDHQCIAADAGG-VKKEDFIAVFKDRNFWVFVIFIVGTWSFYNIFDQQLFPVFYAG 247 R H A +GG V ED + + FW V F++GT Y ++DQQ FPV+++ Sbjct: 188 RVSSAPHAMQEAVSGGKVTLEDALRLLTLPRFWALVFFVIGT-CIYGVYDQQ-FPVYFSS 245 Query: 248 LFESHDVGTRLYGYLNSFQVVLEALCMAIIPFFVNRVGPKNALLIGVVIMALRILSCALF 307 F + G +YGYLNSFQV LEA M P+ VNR+G KN L+ ++MA+R+++ L Sbjct: 246 QFPTLQEGNEMYGYLNSFQVFLEAAGMFCAPWLVNRIGAKNGLIFAGMVMAMRMVASGLV 305 Query: 308 VNPWIISLVKLLHAIEVPLCVISVFKYSVANFDKRLSSTIFLIGFQIASSLGIVLLSTPT 367 P +IS+ KLLHA+E+P+ ++S+FKY+ NFDKRLSST++L+GF SS+ +LS Sbjct: 306 EGPLLISITKLLHAVELPVLLVSIFKYNSLNFDKRLSSTLYLVGFACTSSVIATVLSPLA 365 Query: 368 GILFDHAGYQTVFFAISGIVCLMLLFGIFFLSKKREQIVMETPVPSAI 415 G ++ G+ + + +V IF L + P SAI Sbjct: 366 GYSYEKYGFAQSYLIMGLLVFCTTFISIFLLRSSKSSSDPLMPQTSAI 413 Lambda K H 0.333 0.147 0.471 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: 518 Number of extensions: 25 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: 415 Length of database: 413 Length adjustment: 31 Effective length of query: 384 Effective length of database: 382 Effective search space: 146688 Effective search space used: 146688 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 39 (21.5 bits) S2: 50 (23.9 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