Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate BWI76_RS03270 BWI76_RS03270 sugar ABC transporter ATP-binding protein CymD
Query= reanno::BFirm:BPHYT_RS16095 (369 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS03270 BWI76_RS03270 sugar ABC transporter ATP-binding protein CymD Length = 376 Score = 321 bits (822), Expect = 2e-92 Identities = 182/367 (49%), Positives = 238/367 (64%), Gaps = 17/367 (4%) Query: 1 MASVTLRNIRKAYDEN-EVMRDINLDIADGEFVVFVGPSGCGKSTLMRMIAGLEDISGGD 59 MA+V+LR I K Y+ + + I+L+I DGEF+VFVGPSGC KST +RMIAGLEDISGG+ Sbjct: 1 MATVSLRKIEKRYENGFKAVHGIDLEIHDGEFMVFVGPSGCAKSTTLRMIAGLEDISGGE 60 Query: 60 LTIDGMRVNDVAPAKRGIAMVFQSYALYPHMTLYDNMAFGLKLAGTKKPEIDAAVRNAAK 119 + I +VND+ P RGIAMVFQ+YALYPH T++DNMAFGLK+ K EI V +AA+ Sbjct: 61 IYIGNRKVNDLPPKDRGIAMVFQNYALYPHKTVFDNMAFGLKMQKRPKDEIKRRVEDAAE 120 Query: 120 ILHIDHLLDRKPKQLSGGQRQRVAIGRAITRKPKVFLFDEPLSNLDAALRVKMRLEFARL 179 L I LL RKPK++SGGQRQRVA+GRAI RKP VFLFDEPLSNLDA LRV MR++ A+L Sbjct: 121 KLEITELLYRKPKEMSGGQRQRVAVGRAIVRKPDVFLFDEPLSNLDAKLRVSMRMKIAQL 180 Query: 180 HDELK-----TTMIYVTHDQVEAMTLADKIVVLSAGNLEQVGSPTMLYHAPANRFVAGFI 234 H LK TMIYVTHDQ EA+TL D+I VL+ GN+ QV +PT LY+ P N+FVA FI Sbjct: 181 HRSLKEEGHPATMIYVTHDQTEALTLGDRICVLNHGNIMQVDTPTDLYNYPNNKFVASFI 240 Query: 235 GSPKMNFMEGVVQSVTHDGVTVRYETGETQRVAVEPAAVKQG---DKVTVGIRPEHLHVG 291 GSP +N ++ ++ ++ + V G + + +G V GIRPEH+ + Sbjct: 241 GSPSINLIDTAIRK-NNERLYVEIAPGVEILIPHSKQVLLEGYINKPVCFGIRPEHISLA 299 Query: 292 MAEDGIS---ARTMAVESLGDAAYLYAESSVAPDGLIARI--PPLERHTKGETQKLGATP 346 +D ++ VE++G +LY V LIAR+ + G+T + Sbjct: 300 SDDDDLNTFEGVLTVVENMGSEKFLY--FIVGGKELIARVDTQDINPFHIGKTLRFNLNT 357 Query: 347 EHCHLFD 353 CH+FD Sbjct: 358 AFCHVFD 364 Lambda K H 0.320 0.135 0.384 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: 400 Number of extensions: 21 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: 369 Length of database: 376 Length adjustment: 30 Effective length of query: 339 Effective length of database: 346 Effective search space: 117294 Effective search space used: 117294 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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