Align AglE aka R00695 aka SMC03061, component of Sucrose/maltose/trehalose porter (sucrose-inducible) (characterized)
to candidate WP_069331924.1 C8J29_RS05990 carbohydrate ABC transporter substrate-binding protein
Query= TCDB::Q9Z3R5 (458 letters) >NCBI__GCF_003046325.1:WP_069331924.1 Length = 450 Score = 640 bits (1652), Expect = 0.0 Identities = 299/446 (67%), Positives = 350/446 (78%), Gaps = 2/446 (0%) Query: 13 ALLAGTAGLAGTAGAADLKFKPGEDSRFNWASLEEFKKGHDLKGQTLTIFGPWRGEDEAL 72 A+ A A ++G +LKF PG D+RF+W S E K G DL GQ LTI GPW G D+AL Sbjct: 7 AIAAALALVSGPLAGQELKFPPGADARFHWDSFEALK-GQDLSGQRLTILGPWLGPDKAL 65 Query: 73 FKSVYAYFVEATGVELKYSSSENYEQQIVIDTQAGSPPDVAILPQPGLIADLAAKGLLTP 132 F SV AYF ATG E+ Y+ S+N+EQQIVID AGSPPD+A+ PQPGL DLA+KG L P Sbjct: 66 FDSVIAYFEAATGAEVTYNGSDNFEQQIVIDAGAGSPPDIAVFPQPGLARDLASKGQLAP 125 Query: 133 LGDETKQWLLDNYAAGQSWVDLSTYNGKDGTSALYAFPYKIDVKSLVWYVPENFEDAGYE 192 L T WL +NYAAG+SWV L T+ G+DGT ALY F YKIDVKSLVWYVPENF D GYE Sbjct: 126 LDPATADWLRENYAAGESWVSLGTFPGRDGTEALYGFFYKIDVKSLVWYVPENFADFGYE 185 Query: 193 VPKTMEELKALTEKIAEDGEKPWCIGLGSGGATGWPATDWVEDLMLRTQPAETYDKWVKN 252 +P TMEEL+ALTE++ DG PWC+GL SGGATGWPATDWVED+MLR P E YD+W N Sbjct: 186 IPATMEELRALTERMVADGVTPWCVGLASGGATGWPATDWVEDMMLRINPPEVYDRWTSN 245 Query: 253 EIPFTDAAVTGALEEFGWFARNDAFVDGGAAAVASTDFRDSPKGLFSSPPKCYLHHQASF 312 EIPF D V A+EEFGWFAR FV GG AVA+TDFRDSPKGLFS+PP+C++H QASF Sbjct: 246 EIPFDDPQVVAAIEEFGWFARTPDFVAGGPNAVAATDFRDSPKGLFSAPPQCFMHKQASF 305 Query: 313 IPSFFPEGKVVGEDADFFYMPPYESKKELGNPVLGAGTLAMITKDTPAARAFIEFLKTPI 372 IPSFFPEG V+GEDADFFY+P Y + ++LG PVLGAGT+ +T+DTP ARAF+EFLKTPI Sbjct: 306 IPSFFPEGTVIGEDADFFYLPAY-ADRDLGQPVLGAGTVFGLTRDTPVARAFLEFLKTPI 364 Query: 373 AHEVWMAQTSFLTPYKSVNVDVYGNPPLKKQGEILLNATTFRFDGSDLMPGKIGAGAFWT 432 AHEVWMAQT FLTP+ VN DVYG+P L+K GEILLNATTFRFDGSDLMPG +GAGAFWT Sbjct: 365 AHEVWMAQTGFLTPFTGVNTDVYGDPTLRKMGEILLNATTFRFDGSDLMPGAVGAGAFWT 424 Query: 433 GMVDFVGGKSSADVAAGVQKAWDSIK 458 GM+D++GGK + V A +Q+ WD+ K Sbjct: 425 GMIDYMGGKGAERVGADIQRTWDTFK 450 Lambda K H 0.316 0.135 0.416 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: 805 Number of extensions: 39 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: 458 Length of database: 450 Length adjustment: 33 Effective length of query: 425 Effective length of database: 417 Effective search space: 177225 Effective search space used: 177225 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 (21.6 bits) S2: 51 (24.3 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