Align Gluconokinase; EC 2.7.1.12; Gluconate kinase (uncharacterized)
to candidate WP_008412468.1 DESHY_RS10055 xylulokinase
Query= curated2:P46834 (513 letters) >NCBI__GCF_000315365.1:WP_008412468.1 Length = 510 Score = 239 bits (611), Expect = 1e-67 Identities = 153/512 (29%), Positives = 247/512 (48%), Gaps = 14/512 (2%) Query: 1 MTSYMLGIDIGTTSTKAVLFSEKGDVIQKESIGYALYTPDISTAEQNPDEIFQAVIQSTA 60 M S LGIDIGTT KA++ E+G V+ + + Y L+ P AEQNP++ ++A + A Sbjct: 1 MQSLFLGIDIGTTGVKALVMDEQGRVVAQATREYPLHVPRPGWAEQNPEDWYKAACGAIA 60 Query: 61 KIMQQHPDK-QPSFISFSSAMHSVIAMDENDKPLTSCITWADNRSEGWAHKIKEEMNGHN 119 I+ + Q I + MH + +D K + I W D R+ +I + + Sbjct: 61 TIISKGISPGQIQGIGLTGQMHGSVFLDAQGKVIREAILWCDQRTADECRQITDLVGESK 120 Query: 120 VYKRTGTPIHPMAPLSKITWIVNEHPEIAVKAKKYIGIKEYIFKKLFDQYVVDYSLASAM 179 + + P KI W+ N PE + K + K+YI ++ + D S AS M Sbjct: 121 LIELVSNPALAGFTAPKILWLRNHEPENYKRVAKVLLPKDYISWRMTGVFATDVSDASGM 180 Query: 180 GMMNLKTLAWDEEALAIAGITPDHLSKLVPTTAIFHHCNPELAAMMGIDPQTPFVIGASD 239 ++++ W E LA I L+++ + + + AA G+ P V GA D Sbjct: 181 LLLDVVNRKWSSEMLAALEIPAAWLAEVFESPDVVGRVSARGAAETGLPEGIPVVAGAGD 240 Query: 240 GVLSNLGVNAIKKGEIAVTIGTSGAIRPIIDKPQTDEKGRI--FCYALTENHWVIGGPVN 297 +G I G ++GTSG + P D GR+ FC+A+ W + G Sbjct: 241 NAAGAVGNGIISPGMATASLGTSGVVFTPSQTPAVDRAGRLHTFCHAVP-GQWHLMGVTM 299 Query: 298 NGGIVLRWIRDEFASSEIETAKRLGIDPYDVLTKIAERVRPGADGLLFHPYLAGERAPLW 357 G LRW RD FA E A+ G DPY++++ A + PGADGL+F PYL+GER P Sbjct: 300 AAGGSLRWYRDTFAGEERAVAQLTGRDPYELMSDEAALIEPGADGLIFLPYLSGERTPHA 359 Query: 358 NPDVPGSFFGLTMSHKKEHMIRAALEGVIYNLYTVFLALTECMDGPVARIQATGGFARSD 417 +P G F G+ + H K H +R+ +EGV ++L L + + + ++ TGG RS Sbjct: 360 DPLARGVFVGMNLKHTKGHFVRSIMEGVAFSLKDT-LEIMSGLGIALNDLRITGGGGRSA 418 Query: 418 VWRQMMADIFESEVVVPESYESSCLGACILGLYATGKIDSFDVVSDMIGST------HRH 471 VWRQ++AD+F + V E+ + GA ILG G + V++ + +T Sbjct: 419 VWRQILADVFNMPLQVMENSDGPAYGAAILGAVGAG---CWQSVTEAVAATCSRQQLQEV 475 Query: 472 APKEESAKEYRKLMPLFINLSRALENEYTQIA 503 P ++A Y+K+ ++I+ L+ + +++ Sbjct: 476 VPIPQNAARYQKIYQIYIDTYPPLQPLFKRLS 507 Lambda K H 0.318 0.134 0.401 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: 542 Number of extensions: 23 Number of successful extensions: 4 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: 513 Length of database: 510 Length adjustment: 35 Effective length of query: 478 Effective length of database: 475 Effective search space: 227050 Effective search space used: 227050 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: 52 (24.6 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