Align Ribose import ATP-binding protein RbsA 1; EC 7.5.2.7 (characterized, see rationale)
to candidate WP_094506741.1 CEV31_RS09015 sugar ABC transporter ATP-binding protein
Query= uniprot:Q9WXX0 (520 letters) >NCBI__GCF_002252445.1:WP_094506741.1 Length = 523 Score = 374 bits (961), Expect = e-108 Identities = 205/508 (40%), Positives = 316/508 (62%), Gaps = 12/508 (2%) Query: 14 ILKAKGIVKRFPGVVAVDNVDFEVYENEIVSLIGENGAGKSTLIKILTGVLKPDAGEILV 73 +L+ + + K + G+VAV + E+ + L+GENGAGKSTL+KI+ GV +P G+I++ Sbjct: 12 VLRLEDVSKVYSGIVAVKRANLELRRGSVNVLVGENGAGKSTLMKIIAGVERPTIGKIIL 71 Query: 74 NGERVEFHSPVDAFKKGISVIHQELNLCDNMTVAENIFLAYEAVRGQKRTLSSRVDENYM 133 +GE V F SP DA K+GI++I QELNL NM+VAENIF E RG + +D Sbjct: 72 DGEEVSFDSPADAQKRGIAMIFQELNLFSNMSVAENIFAKREITRGIRG-----IDHKAQ 126 Query: 134 YTRSKELLDLIGAKFSPDALVRNLTTAQRQMVEICKALVKEPRIIFMDEPTSSLTVEETE 193 ++ E LD + A +V +L Q+Q+VEI KA+ + RI+ MDEPTS+L+ E + Sbjct: 127 IKKANEYLDRLDAGIDARTMVADLPIGQQQLVEIAKAISIDARIVIMDEPTSALSAAEVD 186 Query: 194 RLFEIIEMLKSRGISVVFVSHRLDEVMRISDRIVVMRDGKRIGELKKGEFDVDTIIKMMV 253 LF++I LKSRG+++V++SHRL+E+MRI D I V+RDG+ G+ + + I++ M+ Sbjct: 187 ILFKVIADLKSRGVAIVYISHRLEELMRIGDYITVLRDGQITGQEEIKNINTQWIVRSMI 246 Query: 254 GREVEFFPHGIETRPGEIALEVRNLKWKD-----KVKNVSFEVRKGEVLGFAGLVGAGRT 308 G + + F + + G N+ V NVS VR GEVLG GL+GAGR+ Sbjct: 247 GSDAKDFAKAVTHKMGGEMFRAENITLPRAIGGLAVDNVSLSVRAGEVLGIYGLMGAGRS 306 Query: 309 ETMLLVFGVNQKESGDIYVNGRKVEIKNPEDAIKMGIGLIPEDRKLQGLVLRMTVKDNIV 368 E + G + +G+IY++G+KV ++ I+ G+ LIPEDR+ +GLV +++ N+ Sbjct: 307 EFFECIMGQHAHSTGEIYIDGKKVTERDTTRRIRRGLALIPEDRQREGLVQILSIASNLT 366 Query: 369 LPSLKKISRWGLVLDERKEEEISEDYVKRLSIKTPSIYQITENLSGGNQQKVVLAKWLAT 428 L SL +++R+ + +R+++ I E +K L+IK P+ ++SGGNQQKVV+ K L T Sbjct: 367 LASLDRLARFFHISPKREKQAIQE-AIKDLAIKAPNPDFEVTSMSGGNQQKVVIGKALMT 425 Query: 429 NADILIFDEPTRGIDVGAKAEIHRMIRELAAQGKAVIMISSELPEILNLSDRIVVMWEGE 488 N +L+ DEP+RGIDVGAKA++ R +R LA +G A++ +S+L E++ LSDRI V+ G+ Sbjct: 426 NPKVLLMDEPSRGIDVGAKADVFRTMRRLAGEGLAILFSTSDLEEVMALSDRIAVLSNGK 485 Query: 489 ITAVLDNREKRVTQEEIMYYASGQKKQN 516 + A+ D RE + + A G N Sbjct: 486 LIAIFD-RENATEADIVAASAKGHGHVN 512 Lambda K H 0.319 0.138 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: 663 Number of extensions: 36 Number of successful extensions: 8 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: 520 Length of database: 523 Length adjustment: 35 Effective length of query: 485 Effective length of database: 488 Effective search space: 236680 Effective search space used: 236680 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 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