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_050654824.1 C1M55_RS25125 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC
Query= TCDB::Q72L52 (376 letters) >NCBI__GCF_002893965.1:WP_050654824.1 Length = 361 Score = 303 bits (775), Expect = 6e-87 Identities = 184/376 (48%), Positives = 227/376 (60%), Gaps = 34/376 (9%) Query: 1 MAKVRLEHVWKRFGKV--VAVKDFNLETEDGEFVVFVGPSGCGKTTTLRMIAGLEEISEG 58 MA V+ V R+ AV +L+ DGEF+V VGPSGCGK+T+LRM+AGLE S+G Sbjct: 1 MANVQFAGVTHRYEGTDRPAVDRLDLDIADGEFLVLVGPSGCGKSTSLRMLAGLESASDG 60 Query: 59 NIYIGDRLVNDVPPKDRDIAMVFQNYALYPHMNVYENMAFGLRLRRYPKDEIDRRVKEAA 118 I IG V + P+ RD+AMVFQ+YALYP+M V +NM F L+ K E RV EAA Sbjct: 61 RIEIGGTDVTHLAPRARDVAMVFQSYALYPNMTVEQNMGFALQNAGVGKAERRERVLEAA 120 Query: 119 RILKIEHLLNRKPRELSGGQRQRVAMGRAIVREPKVFLMDEPLSNLDAKLRVEMRAEIAK 178 R+L++E LL RKP +LSGGQRQRVAMGRAIVR PKVF MDEPLSNLDAKLRV R++IA Sbjct: 121 RMLELEPLLGRKPAKLSGGQRQRVAMGRAIVRHPKVFCMDEPLSNLDAKLRVSTRSQIAA 180 Query: 179 LQRRLGVTTIYVTHDQVEAMTLGHRIVVMKDGEIQQVDTPLNLYDFPANRFVAGFIGSPS 238 LQRRLG TT+YVTHDQVEAMT+G R+ VM DG +QQV P LYD P N FVA FIGSP Sbjct: 181 LQRRLGTTTVYVTHDQVEAMTMGDRVAVMLDGRLQQVAKPRELYDNPVNTFVAVFIGSPG 240 Query: 239 MNFVRAGVEVQGEKVYLVAPGFRIRANAVLGSALKPY-----AGKEVWLGVRPEHLGLKG 293 MN + A VE AVLG P + V +GVRPE L G Sbjct: 241 MNLIEAPVE---------------GTVAVLGDLRIPLPTGASERERVVVGVRPESWDLVG 285 Query: 294 YTTIPEEENVLRGEVEVVEPLGAETEIHV--------AVNGTLLVAKVDGHAPVKPGDKV 345 + L + +++E LGAE+ ++ +V +VD V PG+ + Sbjct: 286 ----AWRKGSLAVDADLLEELGAESFVYAKGAPDSQWQSRSGRIVIRVDRKMSVAPGESL 341 Query: 346 ELLADTQRLHAFDLET 361 LL ++ F ET Sbjct: 342 HLLPKAGEVYFFSAET 357 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: 403 Number of extensions: 19 Number of successful extensions: 2 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: 361 Length adjustment: 30 Effective length of query: 346 Effective length of database: 331 Effective search space: 114526 Effective search space used: 114526 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: 49 (23.5 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