Align Arabinose import ATP-binding protein AraG; EC 7.5.2.12 (characterized, see rationale)
to candidate WP_061532804.1 CAter10_RS06720 sugar ABC transporter ATP-binding protein
Query= uniprot:A0A165ZSX8 (514 letters) >NCBI__GCF_001584165.1:WP_061532804.1 Length = 515 Score = 378 bits (971), Expect = e-109 Identities = 218/507 (42%), Positives = 321/507 (63%), Gaps = 12/507 (2%) Query: 16 LRFNGIGKSFPGVQALANISFVAHPGQVHALMGENGAGKSTLLKILGGAY-IPSSGDLQI 74 L GI K+F G++ L + + G+VHALMGENGAGKSTL+K+L GA+ + G+++I Sbjct: 11 LEMRGISKTFSGLRVLKEVDLTVYAGEVHALMGENGAGKSTLMKVLSGAHQADTGGEIRI 70 Query: 75 GEQTMAFKGTADSIASGVAVIHQELHLVPEMTVAENLFLGHLPARFGLVNRGVLRQQALT 134 + + G + GVAVI+QEL L P ++VAEN++LG + V+R + + Sbjct: 71 DGRRVVNYGPRAAKEHGVAVIYQELSLCPNLSVAENIYLGRELRQGWSVDRKAMEAGCVD 130 Query: 135 LLKGLADEIDPQEKVGRLSLGQRQLVEIAKALSRGAHVIAFDEPTSSLSAREIDRLMAII 194 +LK L + P KV LS+ +RQLVEIA+A+ A ++ DEPT+ LS+RE DRL A+I Sbjct: 131 VLKRLGADFTPHTKVSSLSIAERQLVEIARAIHAHARILVMDEPTTPLSSRETDRLFALI 190 Query: 195 GRLRDEGKVVLYVSHRMEEVFRICNAVTVFKDGRYVRTFENMSELTHDQLVTCMVGRDIQ 254 +LR+EG ++Y+SHRM E++ + + V+V +DG++V E EL+ + LV MVGRD+ Sbjct: 191 RQLREEGLAIVYISHRMAEIYELSDRVSVLRDGKHVGMLER-DELSAEVLVKMMVGRDLS 249 Query: 255 DIY--DYRPRERGDVALQVKGLLGPGLHEPVSFQVHKGEILGLFGLVGAGRTELLRLLSG 312 Y ++ P + G+V ++V+ + SF +H GE+LG+ GLVGAGRTEL RL+ G Sbjct: 250 GFYKKEHAPYDPGNVVMRVRDMADGRRVRGCSFDLHAGEVLGIAGLVGAGRTELARLIFG 309 Query: 313 LERQREGSLVLHDKELK-LRSPRDAIAAGVLLCPEDRKKEGIIPLGSVGENINISARPSH 371 + + G+L + + + LR P DAI AGV+ EDRK +G+ SV +NIN+ A Sbjct: 310 ADPRIAGTLEVAGQAVSNLRGPADAIRAGVVYLTEDRKAQGLFLDMSVRDNINVCACVPD 369 Query: 372 STLGCLLRGDWERG--NADKQIKSLKVKTPTAGQKIMYLSGGNQQKAILGRWLSMPMKVL 429 + G +L D RG A + IKSL ++ + G + LSGGNQQK +L R L + VL Sbjct: 370 AGYGGVL--DRRRGAQRAAEAIKSLSIRVASPGVNVGALSGGNQQKVLLARLLEIKPHVL 427 Query: 430 LLDEPTRGIDIGAKAEIYQIIHNLAADGIAVIVVSSDLMEVMGISDRILVLCEGAMRGEL 489 +LDEPTRG+DIGAK+EIY+II+ LA GI V+V+SS+L E++G SDR+LV+ EG + EL Sbjct: 428 ILDEPTRGVDIGAKSEIYRIINELANAGIGVVVISSELPEIVGTSDRVLVMREGELVAEL 487 Query: 490 ---SRDQANESNLLQLALPRQRVADAA 513 S + + N+++LA Q+V A Sbjct: 488 GGHSGREITQENIIELATGAQQVQPQA 514 Lambda K H 0.320 0.138 0.391 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: 667 Number of extensions: 35 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: 514 Length of database: 515 Length adjustment: 35 Effective length of query: 479 Effective length of database: 480 Effective search space: 229920 Effective search space used: 229920 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 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