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 BWI76_RS23390 BWI76_RS23390 oligogalacturonide ABC transporter ATP-binding protein
Query= TCDB::Q00752 (377 letters) >FitnessBrowser__Koxy:BWI76_RS23390 Length = 375 Score = 320 bits (819), Expect = 5e-92 Identities = 193/392 (49%), Positives = 250/392 (63%), Gaps = 35/392 (8%) Query: 1 MVELNLNHIYKKYPNSSHYSVEDFDLDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDITKG 60 M E+ N + K Y N +V DL I + EF+V VGPSGC KSTTLRM+AGLE I+ G Sbjct: 1 MAEVIFNKLEKVYSNGFK-AVHGIDLKIADGEFMVIVGPSGCAKSTTLRMLAGLETISGG 59 Query: 61 ELKIDGEVVNDKAPKDRDIAMVFQNYALYPHMSVYDNMAFGLKLRHYSKEAIDKRVKEAA 120 E++I ++VN+ APK R IAMVFQNYALYPHM+V +N+AFGLKL K+ I+ +V EAA Sbjct: 60 EVRIGEKIVNNLAPKARGIAMVFQNYALYPHMTVRENLAFGLKLSKLPKDQIEAQVNEAA 119 Query: 121 QILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAEIAK 180 +IL L E L+R P LSGGQ QRVA+GRAIV+ VFL DEPLSNLDAKLR SMR I+ Sbjct: 120 KILELEELLDRLPRQLSGGQAQRVAVGRAIVKKPDVFLFDEPLSNLDAKLRASMRIRISD 179 Query: 181 IHRRI-----GATTIYVTHDQTEAMTLADRIVIMSSTKNEDGSGTIGRVEQVGTPQELYN 235 +H+++ ATT+YVTHDQTEAMT+ DRI +M +G + QV TP LY+ Sbjct: 180 LHKQLKKSGKPATTVYVTHDQTEAMTMGDRICVMK----------LGHIMQVDTPDNLYH 229 Query: 236 RPANKFVAGFIGSPAMNFFDVTIKDGHLVSKDG-LTIAVTEGQLKM---LESK--GFKNK 289 +P N FVAGFIG+P MN I+ LV + G L + V +G L + L+SK KN+ Sbjct: 230 KPKNMFVAGFIGAPEMN-----IRPSQLVEQAGRLHLTVGDGLLPLNDRLQSKVDTHKNQ 284 Query: 290 NLIFGIRPEDISSSLLVQETYPDATVDAEVVVSELLGSETMLYLKLGQTEFAARV---DA 346 + FG+RPE +S S E + + + E+V E +G E +YLK+ E ARV +A Sbjct: 285 QVFFGVRPEFVSIS---DEPFAEGSCTGEMVRVENMGHEFFVYLKVADYELTARVPSDEA 341 Query: 347 RDFHEPG--EKVSLTFNVAKGHFFDAETEAAI 376 + E G KV F++ K H FDA+TE I Sbjct: 342 KPMIEKGLHRKVHFKFDLNKCHIFDAKTEQNI 373 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: 414 Number of extensions: 23 Number of successful extensions: 6 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 Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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