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_061942033.1 CPter91_RS16320 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC
Query= TCDB::Q72L52 (376 letters) >NCBI__GCF_001584185.1:WP_061942033.1 Length = 380 Score = 339 bits (869), Expect = 9e-98 Identities = 194/380 (51%), Positives = 243/380 (63%), Gaps = 16/380 (4%) Query: 1 MAKVRLEHVWKRF--GKVVAVKDFNLETEDGEFVVFVGPSGCGKTTTLRMIAGLEEISEG 58 MA + + +V K + G V +K +LE EDG+F++ VG SGCGK+T L MIAGLE +SEG Sbjct: 1 MASLSIRNVRKVYPNGNEV-LKGIDLEIEDGQFLILVGGSGCGKSTLLNMIAGLETVSEG 59 Query: 59 NIYIGDRLVNDVPPKDRDIAMVFQNYALYPHMNVYENMAFGLRLRRYPKDEIDRRVKEAA 118 I IGDR VNDVPPK+RDIAMVFQ+YALYP M V EN++FGL +R+ PK E + V+ A Sbjct: 60 QIMIGDRCVNDVPPKERDIAMVFQSYALYPTMTVRENISFGLGIRKVPKAEQKQIVERVA 119 Query: 119 RILKIEHLLNRKPRELSGGQRQRVAMGRAIVREPKVFLMDEPLSNLDAKLRVEMRAEIAK 178 L+I HLL+RKP LSGGQRQRVAMGRAI R+P +FL DEPLSNLDAKLRVEMRAEI Sbjct: 120 NTLQITHLLDRKPALLSGGQRQRVAMGRAIARDPSLFLFDEPLSNLDAKLRVEMRAEIKL 179 Query: 179 LQRRLGVTTIYVTHDQVEAMTLGHRIVVMKDGEIQQVDTPLNLYDFPANRFVAGFIGSPS 238 + +RLG T +YVTHDQ+EAMTLG RI VMKDG +QQ +P +YD P+N FVAGFIGSPS Sbjct: 180 MHQRLGSTIVYVTHDQIEAMTLGDRIAVMKDGVVQQFGSPQEIYDNPSNLFVAGFIGSPS 239 Query: 239 MNFVRAGVEVQGE--KVYLVAPGFRIRANAVLGSALKP----YAGKEVWLGVRPEHLGLK 292 MNF+R + G L G A +P + GKEV LG+RPEH+ Sbjct: 240 MNFMRGNLVANGHGPAFELTHGGRTTLLPLAPAQAQRPEIAAWVGKEVILGIRPEHVTDA 299 Query: 293 GYTTIPE---EENVLRGE----VEVVEPLGAETEIHVAVNGTLLVAKVDGHAPVKPGDKV 345 E + N E VE+ EP G +T + N + + A KP D++ Sbjct: 300 QSARTSEAAGDSNYHPTEVGCTVELTEPTGPDTLVFTTFNEARVTCRTHPRAAAKPKDEM 359 Query: 346 ELLADTQRLHAFDLETDRTI 365 +L D + FD +T+ I Sbjct: 360 QLAFDLSKAVLFDAKTEERI 379 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: 416 Number of extensions: 17 Number of successful extensions: 3 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: 380 Length adjustment: 30 Effective length of query: 346 Effective length of database: 350 Effective search space: 121100 Effective search space used: 121100 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 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