Align Concentrative nucleoside transporter, CNT, of 418 aas and 12 TMSs. A repeat-swapped model of VcCNT predicts that nucleoside transport occurs via a mechanism involving an elevator-like substrate binding domain movement across the membrane (characterized)
to candidate WP_011386447.1 AMB_RS20720 nucleoside:proton symporter
Query= TCDB::Q9KPL5 (418 letters) >NCBI__GCF_000009985.1:WP_011386447.1 Length = 413 Score = 253 bits (646), Expect = 7e-72 Identities = 150/417 (35%), Positives = 239/417 (57%), Gaps = 16/417 (3%) Query: 7 LIGMAVLLGIAVLLSSNRKAINLRTVGGAFAIQFSLGAFILYVPWGQELLRGFSDAVSNV 66 LIG+ L+G+A LLS +R+A++ R V A+Q L +L VP + L G AV+ + Sbjct: 6 LIGIIALIGVAFLLSEDRRAVSWRVVVAGLAVQGLLALLLLKVPAAKLLFLGLDRAVAAL 65 Query: 67 INYGNDGTSFLFG--GLVSGKMFEVFGGGGFIFAFRVLPTLIFFSALISVLYYLGVMQWV 124 GTSF+FG G GFI AF+ LP ++ SAL ++LY+ ++ V Sbjct: 66 QTATRAGTSFVFGYVGGAPAPWTAANPASGFILAFQALPLVLLMSALSALLYHWRILPVV 125 Query: 125 IRILGGGLQKALGTSRAESMSAAANIFVGQTEAPLVVRPFVPKMTQSELFAVMCGGLASI 184 +R L+K++G A +SA+A F+G EAPL++RP+V K+++ ELF VM G+++I Sbjct: 126 VRAASRLLEKSMGVGGAVGVSASATAFLGMIEAPLLIRPYVGKLSRGELFLVMTAGMSTI 185 Query: 185 AGGVLAGYASM--GV---KIEYLVAASFMAAPGGLLFAKLMMPETEKPQDNEDITLDGGD 239 AG V+ YA+ G+ I +L+ AS ++ P GL+ K+M+P+ + L G Sbjct: 186 AGTVMVLYATFLDGIIPDAIGHLLTASLISVPAGLMIGKIMVPDCALTGAGK---LGDGH 242 Query: 240 DKPANVIDAAAGGASAGLQLALNVGAMLIAFIGLIALINGMLGGIGGWFGMPELKLEMLL 299 D A +DA G G++L + + AML+ + L++L N L + G P L L+ +L Sbjct: 243 DY-AGSMDAVVKGTMDGVRLLVGIVAMLVVLVALVSLANAGLALLPEVAGAP-LTLQRVL 300 Query: 300 GWLFAPLAFLIGVPWNEATVAGEFIGLKTVANEFVAYSQFAPYLTEAAPVVLSEKTKAII 359 GW AP+ + +G+P E AG +G KTV NE +AY L P LS +++ I+ Sbjct: 301 GWAMAPVVWAMGIPAGEMVTAGALMGTKTVLNELLAYLD----LAHLPPEALSARSRLIM 356 Query: 360 SFALCGFANLSSIAILLGGLGSLAPKRRGDIARMGVKAVIAGTLSNLMAATIAGFFL 416 ++ LCGFANL S+ IL+ GL +AP+RR +I +G +++I+GT+++ + ++ G L Sbjct: 357 TYGLCGFANLGSLGILIAGLSVMAPERRAEIVALGGRSIISGTMASCLTGSMVGLLL 413 Lambda K H 0.325 0.141 0.414 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: 485 Number of extensions: 28 Number of successful extensions: 5 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: 418 Length of database: 413 Length adjustment: 31 Effective length of query: 387 Effective length of database: 382 Effective search space: 147834 Effective search space used: 147834 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 bits) S2: 50 (23.9 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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