Align sugar transport protein 6 (characterized)
to candidate BWI76_RS24055 BWI76_RS24055 MFS transporter
Query= CharProtDB::CH_091493 (507 letters) >FitnessBrowser__Koxy:BWI76_RS24055 Length = 464 Score = 218 bits (556), Expect = 3e-61 Identities = 150/471 (31%), Positives = 247/471 (52%), Gaps = 34/471 (7%) Query: 18 TVYVFICVMIAAVGGLIFGYDIGISGGVSAMDDFLKEFFPAVWERKKHVHENNYCKYDNQ 77 T+ F+C +AA+ GL+FG DIG+ G A+ EF + H E Sbjct: 13 TMTFFVC-FLAALAGLLFGLDIGVIAG--ALPFIANEF-----QISAHTQE--------- 55 Query: 78 FLQLFTSSLYLAALVASFVASATCSKLGRRPTMQFASIFFLIGVGLTAGAVNLVMLIIGR 137 SS+ A V + + KLGR+ ++ +I F+ G +A A N+ +L+I R Sbjct: 56 ---WVVSSMMFGAAVGAVGSGWLSFKLGRKKSLMIGAILFVAGSLFSAAAPNVEVLLISR 112 Query: 138 LFLGFGVGFGNQAVPLFLSEIAPAQLRGGLNIVFQLMVTIGILIANIVNYFTATVHPYGW 197 + LG VG + PL+LSEIAP ++RG + ++QLM+TIGIL A + + TA + W Sbjct: 113 VLLGLAVGVASYTAPLYLSEIAPEKIRGSMISMYQLMITIGILGAYLSD--TAFSYSGAW 170 Query: 198 RIALGGAGIPAVILLFGSLLIIETPTSLIERNKNEEGKEALRKIRGVDDINDEYESIVHA 257 R LG IPAV+LL G + + ++P + + + + L ++R D + E + + Sbjct: 171 RWMLGVIIIPAVLLLIGVVFLPDSPRWFAAKRRFVDAERVLLRLR---DTSAEAKRELDE 227 Query: 258 CDIASQVKDPYRKLLKPAS--RPPFIIGMLLQLFQQFTGINAIMFYAPVLFQTVGFGSDA 315 + +VK L K S R +G+LLQ+ QQFTG+N IM+YAP +F+ G+ + Sbjct: 228 IRESLKVKQSGWSLFKENSNFRRAVFLGVLLQVMQQFTGMNVIMYYAPKIFELAGYANTT 287 Query: 316 -ALLSAVITGSINVLATFVGIYLVDRTGRRFLLLQSSVHMLICQLIIGIILAKDLGVTGT 374 + VI G NVLATF+ I LVDR GR+ L+ + M + I+G ++ +G+ Sbjct: 288 EQMWGTVIVGLTNVLATFIAIGLVDRWGRKPTLILGFIVMALGMGILGSMM--HIGIHSA 345 Query: 375 LGRPQALVVVIFVCVYVMGFAWSWGPLGWLIPSETFPLETRSAGFAVAVSCNMFFTFVIA 434 + V+ + ++++GFA S GPL W++ SE PL+ R G + + N ++ Sbjct: 346 TAQ---YFAVLMLLMFIVGFAMSAGPLIWVLCSEIQPLKGRDFGITCSTATNWIANMIVG 402 Query: 435 QAFLSMLCGMRSGIFFFFSGWIIVMGLF-AFFFIPETKGIAIDDMRESVWK 484 FL+ML + S F+ G + ++ +F + IPETK ++++ + ++ K Sbjct: 403 ATFLTMLNSLGSANTFWVYGGLNILFIFLTLWLIPETKNVSLEHIERNLMK 453 Lambda K H 0.329 0.144 0.446 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: 611 Number of extensions: 33 Number of successful extensions: 8 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: 507 Length of database: 464 Length adjustment: 34 Effective length of query: 473 Effective length of database: 430 Effective search space: 203390 Effective search space used: 203390 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: 52 (24.6 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