Align RnsB, component of The (deoxy)ribonucleoside permease; probably takes up all deoxy- and ribonucleosides (cytidine, uridine, adenosine and toxic analogues, fluorocytidine and fluorouridine tested), but not ribose or nucleobases (characterized)
to candidate WP_013644298.1 METBO_RS03540 ATP-binding cassette domain-containing protein
Query= TCDB::Q8DU37 (510 letters) >NCBI__GCF_000191585.1:WP_013644298.1 Length = 312 Score = 125 bits (314), Expect = 2e-33 Identities = 76/220 (34%), Positives = 126/220 (57%), Gaps = 13/220 (5%) Query: 4 HVIEMREITKKFDDFVANDHINLDLRKGEIHALLGENGAGKSTLMNMLAGLLEPTSGSIK 63 ++IE ++TKKFDD A D +N+ +RKGE+ LG NGAGK+T + M+ GLL+PTSG+I Sbjct: 3 YMIEAIDLTKKFDDLTAVDGLNIKIRKGEVFGFLGPNGAGKTTSIRMMVGLLKPTSGTIL 62 Query: 64 INGSAVTIDSPSKSAQLGIGMVHQHFMLVEAFTVTENIILGNEV--VKNGILDLKKAGQE 121 I+G+ + K IG+ Q ML E T E++ L ++ V + D Q Sbjct: 63 IDGTDIKQIEKGK-----IGICPQELMLWEHLTCKESLSLMADMFEVPKDVKD-----QR 112 Query: 122 IKALSEKYGLAVDPNAKIADISVGAQQRVEILKTLYRGADILIFDEPTAVLTPSEIQELM 181 I L + L N ++++S G ++R+ + ++ D+++ DEP+ L P + L Sbjct: 113 IHELLKDLFLTDKANTVVSNLSGGMKRRLNLALSVVHEPDVVVLDEPSEGLDPQSRRVLW 172 Query: 182 TIMKSLVK-EGKSIILITHKLDEIRSVADRVTVIRRGKSI 220 ++S+ +GK++IL TH +DE S++DR+ ++ GK I Sbjct: 173 NYIRSMRDVQGKTVILTTHLMDEADSLSDRIGIVDHGKLI 212 Score = 86.3 bits (212), Expect = 1e-21 Identities = 63/224 (28%), Positives = 119/224 (53%), Gaps = 19/224 (8%) Query: 271 IPAIKGLSLEVKAGEIIGIAGIDGNGQSELVQAITGLRKIKSGHLTIKGQDVTKLSTRKI 330 + A+ GL+++++ GE+ G G +G G++ ++ + GL K SG + I G D+ ++ KI Sbjct: 17 LTAVDGLNIKIRKGEVFGFLGPNGAGKTTSIRMMVGLLKPTSGTILIDGTDIKQIEKGKI 76 Query: 331 TELSVGHVPEDRHRDGLILELTMAENLALQT-YYKAPLSHNGVLNYSKINEHGRHLMQEF 389 G P++ L LT E+L+L ++ P + +I+E + L F Sbjct: 77 -----GICPQELM---LWEHLTCKESLSLMADMFEVPKD----VKDQRIHELLKDL---F 121 Query: 390 DVRGANELIPAKGFSGGNQQKAIIAREVDRDPDLLIVSQPTRGLDVGAIEYIHKRLIAER 449 AN ++ SGG +++ +A V +PD++++ +P+ GLD + + + + R Sbjct: 122 LTDKANTVV--SNLSGGMKRRLNLALSVVHEPDVVVLDEPSEGLDPQSRRVLWNYIRSMR 179 Query: 450 D-EGKAVLLVSFELDEILNLSDRIAVIHDGQIQGIVTPETTNKQ 492 D +GK V+L + +DE +LSDRI ++ G++ + TPE K+ Sbjct: 180 DVQGKTVILTTHLMDEADSLSDRIGIVDHGKLIRLDTPENLKKE 223 Lambda K H 0.315 0.135 0.363 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: 381 Number of extensions: 20 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 510 Length of database: 312 Length adjustment: 31 Effective length of query: 479 Effective length of database: 281 Effective search space: 134599 Effective search space used: 134599 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: 42 (22.0 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Apr 09 2024. 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