Align LacI family transcriptional regulator, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized)
to candidate SMc03813 SMc03813 periplasmic binding ABC transporter protein
Query= TCDB::G4FGN5 (343 letters) >FitnessBrowser__Smeli:SMc03813 Length = 337 Score = 143 bits (361), Expect = 6e-39 Identities = 99/286 (34%), Positives = 149/286 (52%), Gaps = 20/286 (6%) Query: 22 DMTILLAPKSLNNPYWFAVENGMKDAAEKLG-IKAIFDAPVEADAAKQAEKILSYIVKGV 80 D L K LNN + ++ G + AA+KLG + + P E D AKQ + + +GV Sbjct: 29 DREFALVFKVLNNAFSPPIQQGCEAAAKKLGDVTCTYLGPTEYDEAKQVQLAQDMVTRGV 88 Query: 81 DGIGISPNDPEGIKVVVKRALDKGIPVIMFDSD--SPDSG-RYAYIGTNNYNAGYEAGKL 137 G+G+S +P+ + ++K A DKGIPV+ FD+D D+G R YIGT+N YE G Sbjct: 89 AGLGVSAGNPKAMARIMKMAQDKGIPVVTFDTDVLPEDAGLRSTYIGTDN----YEFGIA 144 Query: 138 MAQLIEKYKAEKKTIRLAILTGGLAALNLNERIRGFKDALEDYSKRSGKEIVY----VAD 193 +AQ + + K + T+ I +G A+ NL R++G +D L +K G E + + Sbjct: 145 LAQKVLESKKDGGTV--CIQSGAPASENLKARVQGIRDTLAGVTKDKGAEKLTGQNGWTE 202 Query: 194 PFPC----DDDSAKAIQIIRDVTRKYTDLDGWFMSGGWPLFAPK--ETVISALGGPERMK 247 P C +DD A Q +RDV +L + GGW +AP+ + + L K Sbjct: 203 PAGCPVYNNDDITLAAQQVRDVMTNNPELSAFVAVGGWAQYAPQAYKQAMEPLKARLDSK 262 Query: 248 DLLVVGFDTLLPELELVKAGAVKGLVGQRPYDMGYLSVLVLYNMAK 293 DL+VV D P+L L+ G +GQRPYDMGY +++ L + K Sbjct: 263 DLVVVFGDNFGPQLPLLAEGLSHYNIGQRPYDMGYETIMALDKLTK 308 Lambda K H 0.318 0.139 0.398 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: 276 Number of extensions: 18 Number of successful extensions: 5 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: 343 Length of database: 337 Length adjustment: 28 Effective length of query: 315 Effective length of database: 309 Effective search space: 97335 Effective search space used: 97335 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: 49 (23.5 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