Align Xylulose kinase; Xylulokinase; EC 2.7.1.17 (characterized)
to candidate WP_022529344.1 L248_RS06505 gluconokinase
Query= SwissProt::P35850 (502 letters) >NCBI__GCF_000469325.1:WP_022529344.1 Length = 521 Score = 235 bits (599), Expect = 3e-66 Identities = 151/510 (29%), Positives = 242/510 (47%), Gaps = 13/510 (2%) Query: 1 MGKYVLGVDLGTSAVKVSALDHSGQIVAQESFDYDLIQKQPGYNEQNPEDWVSGTTVAIV 60 M Y++GVDLGT++ KV D GQ+VA + Y L Q P E++PE+ T + Sbjct: 1 MTNYLIGVDLGTTSTKVVLFDTRGQVVASANTPYPLYQDTPDMAEEDPEEIFDATIAGLT 60 Query: 61 RLILNDHLDASNIEGLSYSGQMHGLVLLDENKKVLRPAILWNDTRSTPQREEI-EAKLGD 119 ++ HL + G+S+S MH L+L+ ++ L I W D R+ E+ ++ LG Sbjct: 61 AVMRRAHLKPGELAGVSFSAAMHSLILMGQDNTPLTRVITWADNRAAQYATELKDSGLGM 120 Query: 120 EFVHITRNQPLEGFTLTKLLWVKQNEPDIWAKAKYFVLPKDYVRYRMTGNLAMDYSDATG 179 + T L KL W+ PD+ + + + KDY+ +R+ G DYS A Sbjct: 121 QLFKNTGVPTHPMSPLVKLRWLNAEHPDLMRQTAHVIGIKDYILHRLFGRYVQDYSLANA 180 Query: 180 TVLLDVAKGEWSQKICAALDIPMSMCPPLIKSIDLAGTVTPAYAEFSGLTTDTKVFGGAA 239 T L ++ +W + A + P L+ + + PAYA+ G+ + GA+ Sbjct: 181 TGLFNIHTMDWDDQALAVAQVTRDQLPELVDTDYQLTGLNPAYADVIGIDSSVPFIIGAS 240 Query: 240 DNAAGAVGAGILHPNMVLSSIGTSGVVLKYEDNADVNYHGVLQFEDHAIPDKFYSMGVTL 299 D +G + P ++ +IGTSG V D V+ G L F + P ++ G Sbjct: 241 DGTLSNLGVNAIDPGVLAVTIGTSGAVRVVTDKPVVDPQGRL-FTYYLAPGRWVVGGPVN 299 Query: 300 AAGYSFTWFK-KTFAP---------AEDFTDVVASAAKSTVGANGLLYTPYIVGERAPYA 349 G F W + + FAP + + + A+K GA+GLL+ PY+ GERAP Sbjct: 300 NGGIVFRWVRDQLFAPEKLTAEQMDVDSYELLTTIASKIPAGADGLLFHPYLGGERAPIW 359 Query: 350 DADIRGSFTGVDGTHQRYDFVRAVLEGIIFSFRDLFDIYEENGGDFDTVVSIGGGAKSPL 409 DA+ RGSF G+ H R VRA LEGI+++ + + E G + + GG A+S L Sbjct: 360 DANARGSFFGLTRQHTRAHMVRATLEGIVYNLYMVMLMIEGITGKPQAIQATGGFARSAL 419 Query: 410 WLQIQADIFNRKVVSLTNEQGPGMGAAMIAATGLGWFDSLQDCAETFVHFGKAYEPNPDN 469 W Q+ ADIF + V + + +GA +IA LG D L + V + P+P Sbjct: 420 WRQMLADIFEQDVNIPESFESSALGAVVIAMKRLGLIDDL-SAVKDMVGVTNTHHPDPSV 478 Query: 470 VKKYEKMHAIYKQVYQQTKTISEQLLDYRR 499 Y ++ I+ ++ ++ T + D++R Sbjct: 479 FPIYRELLPIWIRLTRELSTEYTAIADFQR 508 Lambda K H 0.318 0.136 0.404 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: 648 Number of extensions: 30 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: 502 Length of database: 521 Length adjustment: 35 Effective length of query: 467 Effective length of database: 486 Effective search space: 226962 Effective search space used: 226962 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