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_090273257.1 BLU11_RS10295 ABC transporter ATP-binding protein
Query= TCDB::Q00752 (377 letters) >NCBI__GCF_900105005.1:WP_090273257.1 Length = 368 Score = 176 bits (445), Expect = 1e-48 Identities = 113/344 (32%), Positives = 186/344 (54%), Gaps = 47/344 (13%) Query: 2 VELNLNHIYKKYPNSSHYSVEDFDLDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDITKGE 61 + L LN + Y H V+D + ++ + +GPSGCGK+TTLR +AG E I+ GE Sbjct: 4 IVLELNTLACGY--GGHKVVQDLSIHLRAGDIGCLLGPSGCGKTTTLRSIAGFEPISDGE 61 Query: 62 LKIDGEVVNDKA----PKDRDIAMVFQNYALYPHMSVYDNMAFGLKLRHYSKEAIDKRVK 117 +++ G +++ + P+ R I MVFQ+YAL+PH++V N+AFG+ +H ++ I V Sbjct: 62 IRLGGRLLSSQTHNVPPEQRRIGMVFQDYALFPHLTVAQNIAFGIN-KHPKRKQI---VG 117 Query: 118 EAAQILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAE 177 E +++ L + +R P +LSGGQ+QRVA+ RA+ + ++ L+DEP SNLD +LR + E Sbjct: 118 ELLELVKLGKLGQRYPHELSGGQQQRVALARALAPEPELLLLDEPFSNLDGELRRRLSGE 177 Query: 178 IAKIHRRIGATTIYVTHDQTEAMTLADRIVIMSSTKNEDGSGTIGRVEQVGTPQELYNRP 237 + I + G + + VTHDQ+EA + D++ ++ GR++Q TP LY+ P Sbjct: 178 VRDILKARGTSAMLVTHDQSEAFAVCDQVGVLRE----------GRLQQWDTPYNLYHEP 227 Query: 238 ANKFVAGFIGSPAMNFFDVTIKDGHLVSKDGLTIAVTEGQLKMLESKGFKNKNLIFG--- 294 A FVA FIG G+ + LT + +L ++ +G + L G Sbjct: 228 ATPFVASFIG------------QGYFIRGQLLTPDTVQTELGVI--RGNRAYQLAAGSAV 273 Query: 295 ---IRPEDISSSLLVQETYPDATVDAEVVVSELLGSETMLYLKL 335 +RP+DI +++ A + LG+ T+ L+L Sbjct: 274 DVLLRPDDIVGQ-------EGSSLTAIITGKVFLGASTLYRLQL 310 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: 299 Number of extensions: 13 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: 377 Length of database: 368 Length adjustment: 30 Effective length of query: 347 Effective length of database: 338 Effective search space: 117286 Effective search space used: 117286 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