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_110206994.1 DNK54_RS11055 ABC transporter ATP-binding protein
Query= TCDB::Q00752 (377 letters) >NCBI__GCF_003194585.1:WP_110206994.1 Length = 368 Score = 205 bits (522), Expect = 1e-57 Identities = 127/364 (34%), Positives = 205/364 (56%), Gaps = 28/364 (7%) Query: 4 LNLNHIYKKYPNSSHYSVEDFDLDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDITKGELK 63 + ++ I K Y +++ + D DLDI+ EF+ +G SG GKST L ++AG G+++ Sbjct: 16 IEVDRIRKVYGSTT--ILNDIDLDIRAGEFLTLLGASGSGKSTLLNIIAGFIKADGGDVR 73 Query: 64 IDGEVVNDKAPKDRDIAMVFQNYALYPHMSVYDNMAFGLKLRHYSKEAIDKRVKEAAQIL 123 +DG+ + R + MVFQ+YAL+PHMSVYDN+A+GL+ + K I V +A +++ Sbjct: 74 VDGKSITSVPAHKRGLGMVFQHYALFPHMSVYDNVAYGLRRHGFPKAEIPGLVADALEMV 133 Query: 124 GLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAEIAKIHR 183 + +R+PA+LSGGQ+QRVA+ RA+V +V LMDEPL LD LR ++ EI ++H+ Sbjct: 134 EMGHLGKRRPAELSGGQQQRVALARAVVFRPRVLLMDEPLGALDKMLREQLQLEIRRLHK 193 Query: 184 RIGATTIYVTHDQTEAMTLADRIVIMSSTKNEDGSGTIGRVEQVGTPQELYNRPANKFVA 243 +G T ++VTHDQ EA+T++DRI ++ G + Q+GTP+ELY+ P+ ++ A Sbjct: 194 EMGITFVFVTHDQEEALTMSDRIALLEK----------GDIVQLGTPEELYDAPSCRYAA 243 Query: 244 GFIGSPAMNFFDVTIKDGHLVSKDGLTIAVTEGQLKMLESKGFKNKNLIFGIRPEDIS-S 302 FIG + + S+ G T Q S G + ++ +RPE + S Sbjct: 244 EFIG----------VSNIMTGSRAGDVFTDTRNQTTHKVSGGAADGTVLM-VRPERLRVS 292 Query: 303 SLLVQETYPDATVDAEVVVSELLGSETMLYLKLGQ-TEFAARVD---ARDFHEPGEKVSL 358 + V + + A V LGS+ ++++ E AR + D +PG V+L Sbjct: 293 AGQVGPAGHENALPAIVSDCVYLGSDRTVHVRTASGEEMVARTEVPRTDDGIQPGVPVTL 352 Query: 359 TFNV 362 T+N+ Sbjct: 353 TWNI 356 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: 327 Number of extensions: 10 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: 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