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_068331063.1 A3K86_RS11520 NupC/NupG family nucleoside CNT transporter
Query= TCDB::Q9KPL5 (418 letters) >NCBI__GCF_001650345.1:WP_068331063.1 Length = 421 Score = 660 bits (1703), Expect = 0.0 Identities = 335/417 (80%), Positives = 373/417 (89%) Query: 1 MSLFMSLIGMAVLLGIAVLLSSNRKAINLRTVGGAFAIQFSLGAFILYVPWGQELLRGFS 60 MSLFMSL+GMAVLL IAVLLS NRKAINLRTVGGAFAIQF LGAF+LYVP G+++L G S Sbjct: 1 MSLFMSLVGMAVLLAIAVLLSDNRKAINLRTVGGAFAIQFCLGAFVLYVPVGRDVLYGMS 60 Query: 61 DAVSNVINYGNDGTSFLFGGLVSGKMFEVFGGGGFIFAFRVLPTLIFFSALISVLYYLGV 120 AV+NVI+YGNDG +FLFGGL S KMFEVFGGGGF+FA RVLP ++FFSALISVLYY+G+ Sbjct: 61 QAVANVISYGNDGINFLFGGLTSDKMFEVFGGGGFVFALRVLPVIVFFSALISVLYYMGI 120 Query: 121 MQWVIRILGGGLQKALGTSRAESMSAAANIFVGQTEAPLVVRPFVPKMTQSELFAVMCGG 180 MQ+VI ILGGGLQKALGTSRAESMSA ANIFVGQTEAPLV+RPFVPKMTQSELFAVMCGG Sbjct: 121 MQFVINILGGGLQKALGTSRAESMSATANIFVGQTEAPLVIRPFVPKMTQSELFAVMCGG 180 Query: 181 LASIAGGVLAGYASMGVKIEYLVAASFMAAPGGLLFAKLMMPETEKPQDNEDITLDGGDD 240 LAS+AGGVLAGYASMGV +EYL+AASFMAAPGGLLFAK++ PETE+P + GDD Sbjct: 181 LASVAGGVLAGYASMGVPLEYLIAASFMAAPGGLLFAKIIKPETEEPIEQLAGDDANGDD 240 Query: 241 KPANVIDAAAGGASAGLQLALNVGAMLIAFIGLIALINGMLGGIGGWFGMPELKLEMLLG 300 KPANVIDAAA GAS+G+QLALNVGAML+AFIGLIALINGMLGGIGGWFGMPEL LE++LG Sbjct: 241 KPANVIDAAAAGASSGMQLALNVGAMLLAFIGLIALINGMLGGIGGWFGMPELTLELILG 300 Query: 301 WLFAPLAFLIGVPWNEATVAGEFIGLKTVANEFVAYSQFAPYLTEAAPVVLSEKTKAIIS 360 ++F+PLAFLIGVPW EAT+AG FIG K V NEFVAY FAPYL + A VVLS KT+AIIS Sbjct: 301 YVFSPLAFLIGVPWEEATIAGSFIGQKLVVNEFVAYLNFAPYLADGAEVVLSAKTEAIIS 360 Query: 361 FALCGFANLSSIAILLGGLGSLAPKRRGDIARMGVKAVIAGTLSNLMAATIAGFFLS 417 FALCGFANLSS+AILLGGLG LAP RR DIAR G+KAV AGTLSNLM+ATIAG F++ Sbjct: 361 FALCGFANLSSVAILLGGLGGLAPSRRHDIARFGMKAVAAGTLSNLMSATIAGLFVA 417 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: 750 Number of extensions: 41 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: 418 Length of database: 421 Length adjustment: 32 Effective length of query: 386 Effective length of database: 389 Effective search space: 150154 Effective search space used: 150154 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 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