Align Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized)
to candidate WP_084703891.1 BS73_RS07930 ABC transporter ATP-binding protein
Query= TCDB::Q72L52 (376 letters) >NCBI__GCF_000744815.1:WP_084703891.1 Length = 389 Score = 221 bits (562), Expect = 3e-62 Identities = 144/356 (40%), Positives = 198/356 (55%), Gaps = 16/356 (4%) Query: 4 VRLEHVWKRFGKVVAVKDFNLETEDGEFVVFVGPSGCGKTTTLRMIAGLEEISEGNIYIG 63 + E V + V + F L+ GE V +GPSG GKTT LR +AG G + IG Sbjct: 32 ISFEDVTVAYRDQVVLNGFTLDVAAGEVVALLGPSGSGKTTALRTVAGFTAPVRGRVGIG 91 Query: 64 DRLVNDVPPKDRDIAMVFQNYALYPHMNVYENMAFGLRLRRYPKDEIDRRVKEAARILKI 123 R V +PP R I MV Q YAL+PH+ V +N+AFGL+ R P+ ++ RV EA + + Sbjct: 92 GRDVTGLPPHRRGIGMVVQQYALFPHLRVEQNVAFGLKAHRTPRAQVPGRVAEALEMTGM 151 Query: 124 EHLLNRKPRELSGGQRQRVAMGRAIVREPKVFLMDEPLSNLDAKLRVEMRAEIAKLQRRL 183 R PRELSGGQ+QRVA+ RA+ P+V L+DEPLS LDA LR M AE+A+L R L Sbjct: 152 AGYARRYPRELSGGQQQRVALARALAIRPEVLLLDEPLSALDAGLRAGMLAELARLHREL 211 Query: 184 -GVTTIYVTHDQVEAMTLGHRIVVMKDGEIQQVDTPLNLYDFPANRFVAGFIGSPSMNFV 242 V+ +YVTHDQ+EA+TL RI V++D + TP LY PA+ F A F+G ++ V Sbjct: 212 PEVSILYVTHDQIEALTLADRIAVLRDARLVDCGTPERLYRRPADAFTASFVGRANLLPV 271 Query: 243 RAGVEVQGEKVYLVAPGFRIRANAVLGSALKPY-AGKEVWLGVRPEHLGLKGYTTIPEEE 301 AG E ++V L A R A + +A + AG L VRP L P E Sbjct: 272 TAGQE--PDRVVLGAATHRTGAVELRITAQDGFPAGSPALLCVRPHQLR-------PATE 322 Query: 302 ---NVLRGEVEVVEPLGAETEIHVAVN-GTLLVAKVDG-HAPVKPGDKVELLADTQ 352 N+LRG V V+ LG+ + V ++ G + A++ G P G+++ L D + Sbjct: 323 GGPNLLRGRVSDVQWLGSTHRVQVDLDAGPRVAAELSGLRVPPAAGEELALGFDPE 378 Lambda K H 0.320 0.139 0.400 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: 369 Number of extensions: 16 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: 376 Length of database: 389 Length adjustment: 30 Effective length of query: 346 Effective length of database: 359 Effective search space: 124214 Effective search space used: 124214 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Apr 09 2024. 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