Align D-ribose transporter ATP-binding protein; SubName: Full=Putative xylitol transport system ATP-binding protein; SubName: Full=Sugar ABC transporter ATP-binding protein (characterized, see rationale)
to candidate GFF3594 PS417_18400 sugar ABC transporter ATPase
Query= uniprot:A0A1N7TX47 (495 letters) >FitnessBrowser__WCS417:GFF3594 Length = 517 Score = 323 bits (829), Expect = 7e-93 Identities = 198/494 (40%), Positives = 287/494 (58%), Gaps = 10/494 (2%) Query: 6 LLQAEHVAKAYAGVPALRDGRLSLRAGSVHALCGGNGAGKSTFLSILMGITQRDAGSILL 65 +L + K YA P L D L+L G V AL G NGAGKST I+ G+ G + Sbjct: 9 VLSVSGIGKTYAQ-PVLSDITLTLNRGEVLALTGENGAGKSTLSKIIGGLVTPTTGHMQF 67 Query: 66 NGAPVQFNRPSEALAAGIAMITQELEPIPYMTVAENIWLGREPRRAGCIVDNKALNRRTR 125 NG + ++A G+ M+ QEL +P +TVAEN++L P G I K L + Sbjct: 68 NGQDFRPGSRTQAEELGVRMVMQELNLLPTLTVAENLFLDNLPSHCGWI-SRKQLRKAAI 126 Query: 126 ELLDSLEFD-VDATSPMHRLSVAQIQLVEIAKAFSHDCQVMIMDEPTSAIGEHEAQTLFK 184 E + + D +D + + L + Q+VEIA+ DC V+I+DEPT+ + E + LF+ Sbjct: 127 EAMAQVGLDAIDPDTLVGSLGIGHQQMVEIARNLIGDCHVLILDEPTAMLTAREVEMLFE 186 Query: 185 AIRRLTAQGAGIVYVSHRLSELAQIADDYSIFRDGAFVESGRMADIDRDHLVRGIVGQEL 244 I RL A+G I+Y+SHRL ELA++A ++ RDG V MA+ + + LV +VG+EL Sbjct: 187 QITRLQARGVAIIYISHRLEELARVAQRIAVLRDGKLVCVEPMANYNSEQLVTLMVGREL 246 Query: 245 -TRIDHKVGRECAANTCLQVDNLSRAGEFHDISLQLRQGEILGIYGLMGSGRSEFLNCIY 303 ID +G L V L+R+ + D+S ++R GEI GI GL+G+GR+E L I+ Sbjct: 247 GEHID--LGPRTIGGPALTVKGLTRSDKVRDVSFEVRAGEIYGISGLIGAGRTELLRLIF 304 Query: 304 GLTVADSGSVTLQGKP---MPIGLPKATINAGMSLVTEDRKDSGLVLTGSILSNIALSAY 360 G +ADSG+V L G P + I P + G++L+TEDRK GL+LT SI +NIAL Sbjct: 305 GADLADSGTVAL-GSPAQVVSIRSPVDAVGHGIALITEDRKGEGLLLTQSISANIALGNM 363 Query: 361 KRLSSWSLINARKETQLAEDMVKRLQIKTTSLELPVASMSGGNQQKVVLAKCLSTEPVCL 420 +S ++N+R ET LA+ + ++I+++S V+ +SGGNQQKVV+ + L + + Sbjct: 364 PEISGGGVVNSRDETALAKRQIDAMRIRSSSPAQLVSELSGGNQQKVVIGRWLERDCSVM 423 Query: 421 LCDEPTRGIDEGAKQEIYHLLDQFVRGGGAAIVVSSEAPELLHLSDRIAVFKGGRLVTIS 480 L DEPTRGID GAK +IY LL + R G A +VVSS+ EL+ + DRI V GRL+ Sbjct: 424 LFDEPTRGIDVGAKFDIYALLGELTRQGKALVVVSSDLRELMLICDRIGVLSAGRLIETF 483 Query: 481 TDTALSQEALLRLA 494 + +Q+ LL A Sbjct: 484 ERDSWTQDELLAAA 497 Lambda K H 0.319 0.135 0.381 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: 605 Number of extensions: 27 Number of successful extensions: 9 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: 495 Length of database: 517 Length adjustment: 34 Effective length of query: 461 Effective length of database: 483 Effective search space: 222663 Effective search space used: 222663 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: 52 (24.6 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:
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