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_013519272.1 ALIDE2_RS13080 sulfate ABC transporter ATP-binding protein
Query= TCDB::Q00752 (377 letters) >NCBI__GCF_000204645.1:WP_013519272.1 Length = 375 Score = 206 bits (524), Expect = 9e-58 Identities = 128/376 (34%), Positives = 208/376 (55%), Gaps = 49/376 (13%) Query: 2 VELNLNHIYKKYPNSSHYSVEDFDLDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDITKGE 61 + + + ++ K++ S ++ D LDI++ E I +GPSGCGK+T LR++AGLE G Sbjct: 1 MSIEIRNVSKQF--GSFQALRDVSLDIQSGELIALLGPSGCGKTTLLRIIAGLETPDTGS 58 Query: 62 LKIDGEVVNDKAPKDRDIAMVFQNYALYPHMSVYDNMAFGLKLR----HYSKEAIDKRVK 117 + GE D ++R + VFQ+YAL+ HM+V DN+AFGL+++ S+ I ++V Sbjct: 59 IHFSGENQTDVHVRERGVGFVFQHYALFRHMTVLDNVAFGLRMKPRRERPSEAQIRQKVM 118 Query: 118 EAAQILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAE 177 + +++ L +R P+ LSGGQRQR+A+ RA+ + KV L+DEP LDAK+R +R Sbjct: 119 DLLKLVQLDWIADRYPSQLSGGQRQRIALARALAVEPKVLLLDEPFGALDAKVRKELRRW 178 Query: 178 IAKIHRRIGATTIYVTHDQTEAMTLADRIVIMSSTKNEDGSGTIGRVEQVGTPQELYNRP 237 + ++H + T+I+VTHDQ EA+ +ADR+V+++ GR+EQ GTPQ++++ P Sbjct: 179 LRRLHDELHVTSIFVTHDQEEALEVADRVVVINQ----------GRIEQQGTPQQVWDNP 228 Query: 238 ANKFVAGFIGSPAMNFFDVTIKDGHLVSKDGLTIAVTEGQLKMLESKGFKNKNLIFGIRP 297 A+ FV GF+G +N F DG + +G+ QL E++ +RP Sbjct: 229 ASPFVYGFLGD--VNLFKGRANDGRIHLDEGM-------QLDSPEARHADGAPAFAYVRP 279 Query: 298 EDISSSLLVQETYPDATVDA---------EVVVSELLGSETMLYL-KLGQTEFA------ 341 D+ V+ P +DA ++V S ++G L L G T+ A Sbjct: 280 HDLD----VERYSPGQALDAHGRPRGIVVQLVRSIVVGPIARLELIPEGSTQSADNAAPD 335 Query: 342 ----ARVDARDFHEPG 353 A++ A+ FH+ G Sbjct: 336 MLIEAQIPAQQFHDMG 351 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: 341 Number of extensions: 16 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: 375 Length adjustment: 30 Effective length of query: 347 Effective length of database: 345 Effective search space: 119715 Effective search space used: 119715 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 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