Align MsiK protein, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized)
to candidate N515DRAFT_1562 N515DRAFT_1562 sulfate transport system ATP-binding protein
Query= TCDB::P96483 (377 letters) >lcl|FitnessBrowser__Dyella79:N515DRAFT_1562 N515DRAFT_1562 sulfate transport system ATP-binding protein Length = 384 Score = 203 bits (517), Expect = 6e-57 Identities = 139/369 (37%), Positives = 195/369 (52%), Gaps = 34/369 (9%) Query: 20 AVDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNGGAIRIGDRDVTHLPPKDRDI 79 A+D + I +GEF+ L+GPSG GKS+ LR+LAGL+D + G + D+ LP + RDI Sbjct: 17 ALDDFSLDIAEGEFVALLGPSGSGKSSLLRILAGLDDPDRGDVLRDGTDLLALPAQRRDI 76 Query: 80 AMVFQNYALYPHMTVADNMGFALKIAGVPKA------EIRQKVEEAAKILDLTQYLDRKP 133 +VFQ+YAL+PHMTVADN+ F L++ P+A +I +VE+ + + L + R P Sbjct: 77 GLVFQHYALFPHMTVADNIAFGLRVR--PRARRPSRRDIAARVEDLLRRVQLEELGRRYP 134 Query: 134 KALSGGQRQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIASLQRRLGITTVYVT 193 LSGGQRQRVA+ RA+ EP + L+DEP LDA++R + R + LQR LG+TTV VT Sbjct: 135 TQLSGGQRQRVALARALAVEPSLLLLDEPFGALDAQVRGTLRVWLRDLQRSLGLTTVLVT 194 Query: 194 HDQVEAMTMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIGSPAMNLVEVPITDGGV 253 HDQ EA+ + DRV V+ G ++QV +P +Y +PA FV GF+G N + + + Sbjct: 195 HDQDEALELADRVVVMNRGRIEQVGAPSEIYREPATPFVHGFVG--RANRIRGHVERDRL 252 Query: 254 KFGNSVVPVNREALSAADKGDRTVTVGVRPEHFDVVE--LGGAVAASLSKDSADAPAGLA 311 G + + D R + +RPEH + LGG D A A Sbjct: 253 HLGGH----SFQGELPGDLAGREIEAWLRPEHLALASRGLGGWTGRLQHLDLAGPVARAR 308 Query: 312 VSVNVVEELGADGYV----YGTAEVG------GEVKDLVVR--VNGRQVPEKGSTLHVVP 359 ++++ DG V + AEV GEV L R VP L VP Sbjct: 309 LAMH------GDGLVLDAEWNAAEVAAHGLAIGEVVTLQPREFTLFADVPGGVRRLRFVP 362 Query: 360 RPGETHVFS 368 P H S Sbjct: 363 APAGPHADS 371 Lambda K H 0.317 0.135 0.379 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: 377 Number of extensions: 25 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: 384 Length adjustment: 30 Effective length of query: 347 Effective length of database: 354 Effective search space: 122838 Effective search space used: 122838 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 (21.6 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