Align MsmK aka SMU.882, component of The raffinose/stachyose transporter, MsmEFGK (MalK (3.A.1.1.27) can probably substitute for MsmK; Webb et al., 2008). This system may also transport melibiose, isomaltotriose and sucrose as well as isomaltosaccharides (characterized)
to candidate WP_022530287.1 L248_RS10935 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC
Query= TCDB::Q00752 (377 letters) >NCBI__GCF_000469325.1:WP_022530287.1 Length = 378 Score = 511 bits (1317), Expect = e-149 Identities = 253/378 (66%), Positives = 314/378 (83%), Gaps = 12/378 (3%) Query: 1 MVELNLNHIYKKYPNSSH--YSVEDFDLDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDIT 58 MV+++L+HIYK+YP++ Y+V DFDL I+++EFIVFVGPSGCGKSTTLRM+AGLEDIT Sbjct: 1 MVKVDLDHIYKEYPDAQEGVYAVSDFDLHIQDQEFIVFVGPSGCGKSTTLRMIAGLEDIT 60 Query: 59 KGELKIDGEVVNDKAPKDRDIAMVFQNYALYPHMSVYDNMAFGLKLRHYSKEAIDKRVKE 118 KG+LKI G+V+ND APKDRDIAMVFQNYALYPHM+V+DNMAFGLKLR Y K I KRV E Sbjct: 61 KGDLKIGGQVMNDVAPKDRDIAMVFQNYALYPHMTVFDNMAFGLKLRKYEKADIKKRVDE 120 Query: 119 AAQILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAEI 178 AA+ILGLT++L+RKPA LSGGQRQRVA+GRAIVRDA +FLMDEPLSNLDAKLRV+MRAEI Sbjct: 121 AAEILGLTDYLDRKPAALSGGQRQRVALGRAIVRDAPIFLMDEPLSNLDAKLRVTMRAEI 180 Query: 179 AKIHRRIGATTIYVTHDQTEAMTLADRIVIMSSTKNEDGSGTIGRVEQVGTPQELYNRPA 238 AK+H+R+ TTIYVTHDQTEAMT+ADRIV+MS +G+V+Q+GTP E+Y+RP Sbjct: 181 AKLHQRLKTTTIYVTHDQTEAMTMADRIVVMS----------MGKVQQIGTPAEVYDRPK 230 Query: 239 NKFVAGFIGSPAMNFFDVTIKDGHLVSKDGLTIAVTEGQLKMLESKGFKNKNLIFGIRPE 298 N+FVAGFIGSPAMNFF+V +KDG + GL + V EG+LK+LE +G+ +K+L+ G+RPE Sbjct: 231 NEFVAGFIGSPAMNFFNVHLKDGFVSDGKGLNLQVPEGRLKILEDQGYDDKDLVLGVRPE 290 Query: 299 DISSSLLVQETYPDATVDAEVVVSELLGSETMLYLKLGQTEFAARVDARDFHEPGEKVSL 358 DI + ET+P AT VVVSELLG+E+MLY ++ QTEF ARVDARD+H+PG+ + + Sbjct: 291 DIHAEEAFIETFPKATAKTTVVVSELLGAESMLYARVDQTEFVARVDARDYHKPGDNLEM 350 Query: 359 TFNVAKGHFFDAETEAAI 376 F++ K HFFD ET AI Sbjct: 351 AFDLNKAHFFDKETTDAI 368 Lambda K H 0.318 0.135 0.375 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: 22 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: 377 Length of database: 378 Length adjustment: 30 Effective length of query: 347 Effective length of database: 348 Effective search space: 120756 Effective search space used: 120756 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 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