Align deoxynucleoside transporter, ATPase component (characterized)
to candidate WP_085125214.1 B9O00_RS23655 sugar ABC transporter ATP-binding protein
Query= reanno::Burk376:H281DRAFT_01113 (515 letters) >NCBI__GCF_900177295.1:WP_085125214.1 Length = 508 Score = 311 bits (796), Expect = 5e-89 Identities = 198/515 (38%), Positives = 291/515 (56%), Gaps = 12/515 (2%) Query: 1 MNQQEVSSAPLSQPFLEVVGVHKRFTGVHALRGVSLSFQRGQIYHLLGENGCGKSTLIKI 60 M++ ++ + P +E + + K F GV A+ + S + G+++ L+GENG GKSTLIK+ Sbjct: 1 MSEATQTAGGVVPPAVEGIRLAKAFGGVQAVDSATFSARPGEVHALVGENGAGKSTLIKL 60 Query: 61 ISGAQPPDEGQLVIEGVPHARLSALEALAAGIETVYQDLSLLPNMSVAENVALTSELATH 120 + G PD G++ G A +A A GI TV+Q+L+LLP M+VAEN+ + E Sbjct: 61 LGGRLRPDAGEVRAAGRKVELHGADDAHALGIWTVFQELTLLPWMTVAENLLIRRE---P 117 Query: 121 EGRLARTFDRRVLAATAARALEAVGLPGNSEFQSTLIEQLPLATRQLVAIARAIASEAKF 180 GRL DR + A R L +G+ LIE L LA RQ+V IAR I + Sbjct: 118 RGRLG-LIDRDRMVGEADRVLTWLGIDHIDP--RALIEDLSLAQRQMVEIARVIIQDPST 174 Query: 181 VIMDEPTTSLTQKEVDNLIAVLANLRAQGVTVLFVSHKLDECYAIGGEVIVLRDGQKMAQ 240 +++DEPT+SL +KEV L ++ LRA G ++F SH+ +E +I + + R+G ++ Sbjct: 175 LLLDEPTSSLGEKEVAWLFELIQGLRADGKCIIFTSHRWNEITSIADRITIFRNGAEV-- 232 Query: 241 GPIAEFTKAQISELMTGRHLSNERYRESAHAQD-IVLDVRGFTRAGQFSDVSFKLHGGEI 299 G E + + LMTGR L + A A D VL+V G + S LH EI Sbjct: 233 GTFTEIDEDRAVTLMTGRQLEAFYPQPPARAHDRAVLEVEELAGEG-LRNASLTLHASEI 291 Query: 300 LGVTGLLDSGRNELARALAGVAPAQSGDVLLDGQQIALRTPSDAKRHRIGYVPEDRLNEG 359 LGV GL G EL +L G A A SG +++DG+ +R+P DA R + VPEDR EG Sbjct: 292 LGVGGLAGHGHRELFFSLFG-AQAHSGRIVVDGRPARIRSPRDAARLGMALVPEDRKTEG 350 Query: 360 LFLDKPIRDNVITAMISSLRDRFGQIDRTRAQALAEQTVKELQIATPGVDKPVQSLSGGN 419 L L +R N+ A++ ++ G I R + LA+ V L+I TPG+ PV+ LSGGN Sbjct: 351 LLLPLSVRANLTLAVLPAVSS-LGLIGGARERGLAQGMVDALKIRTPGLGNPVRQLSGGN 409 Query: 420 QQRVLIGRWLAIDPRVLILHGPTVGVDVGSKDIIYRIMQRLSQRGIGIILISDDLPELLQ 479 QQ+VL+GRWL D R+L+L+ T GVDV +K IY +M RL+ G ++ S D EL Sbjct: 410 QQKVLLGRWLLADSRILLLYDVTRGVDVATKHEIYELMMRLAGEGRALLYYSSDAEELAH 469 Query: 480 NCDRILMMKKGHVSAEYRADELSEADLYHALLSEA 514 C R+L+M++G ++AE A ++ D+ A + E+ Sbjct: 470 LCHRVLVMREGRIAAELSAPGITAEDIVTAAVRES 504 Lambda K H 0.319 0.135 0.376 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: 607 Number of extensions: 38 Number of successful extensions: 6 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: 515 Length of database: 508 Length adjustment: 35 Effective length of query: 480 Effective length of database: 473 Effective search space: 227040 Effective search space used: 227040 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 (21.7 bits) S2: 52 (24.6 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