Align Purine/cytidine ABC transporter ATP-binding protein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized)
to candidate WP_011318959.1 AVA_RS10980 sugar ABC transporter ATP-binding protein
Query= TCDB::A2RKA7 (506 letters) >NCBI__GCF_000204075.1:WP_011318959.1 Length = 517 Score = 328 bits (841), Expect = 3e-94 Identities = 184/479 (38%), Positives = 290/479 (60%), Gaps = 8/479 (1%) Query: 6 VIQMIDVTKRFGDFVANDKVNLELKKGEIHALLGENGAGKSTLMNILSGLLEPSEGEVHV 65 V++M + KRF A VNL + GE+HAL+GENGAGKSTLM IL+G EGE+ + Sbjct: 18 VLEMQGIAKRFHGVPALQGVNLTIYPGEVHALMGENGAGKSTLMKILAGAYIADEGEIRI 77 Query: 66 KGKLENIDSPSKAANLGIGMVHQHFMLVDAFTVTENIILGNEVTKGINLDLKTAKKKILE 125 GK I P A GI +++Q + TVTENI +G+E+T+G LD K + + + Sbjct: 78 NGKGVKITDPGTARQAGINLIYQELNVAPNLTVTENIFMGSELTRGQFLDRKAMELEAQQ 137 Query: 126 LSERYGLSVEPDALIRDISVGQQQRVEILKTLYRGADILIFDEPTAVLTPAEITELMQIM 185 + G S P ++ +++ +QQ+VEI + L + IL+ DEPTA L+ E L +++ Sbjct: 138 VLASLGASFAPTDIVGTLAIAEQQQVEIARALKDNSRILVMDEPTAALSDRETERLFEVI 197 Query: 186 KNLIKEGKSIILITHKLDEIRAVADRITVIRRGKSIDTVELGDKTNQELAELMVGRSV-S 244 + L +G +II I+H+++EI A+ADRI+V+R G+ I ++ + + Q L ++MVGRS+ Sbjct: 198 RKLRNDGIAIIYISHRMEEIYALADRISVLRDGQYIGSLTREEISPQRLVQMMVGRSMQD 257 Query: 245 FITEKAAAQPKDVVLEIKDLNIKESRGSLKVKGLSLDVRAGEIVGVAGIDGNGQTELVKA 304 F + + P VVLE++ NI + R KV+ S +RAGEI+G+AG+ G G+TE+ + Sbjct: 258 FYEHQRQSNPGPVVLEVR--NISDGR---KVQPASFQLRAGEILGLAGLVGAGRTEVSRL 312 Query: 305 ITGLTKVDSGSIKLHNKDITNQRPRKITEQSVGHVPEDRHRDGLVLEMTVAENIALQTYY 364 I G + SG + L+ K + P +G+VPEDR GL LEM+ +NI L Sbjct: 313 IFGADRKVSGEVFLNGKKLEIHSPSDAIAVGIGYVPEDRKDQGLFLEMSSRKNIGLNRLK 372 Query: 365 KPPMSKYGFLDYNKINSHARELMEEFDVRGAGEWVSASSLSGGNQQKAIIAREIDRNPDL 424 + + G +++ +N A + +E F +R A + A LSGGNQQK ++AR + NP + Sbjct: 373 QD--ANLGIVNWGSVNKIATDAVENFHIRLANLEIRAVDLSGGNQQKLLLARWLAINPRV 430 Query: 425 LIVSQPTRGLDVGAIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHDGQIQG 483 L++ +PTRG+D+GA I++ + +G A+L++S EL EI+ +SDR+ V+ +GQ+ G Sbjct: 431 LMLDEPTRGVDIGAKSEIYRIISDLSAQGVAILMVSSELPEIVGLSDRVLVMREGQLVG 489 Score = 92.0 bits (227), Expect = 4e-23 Identities = 63/249 (25%), Positives = 130/249 (52%), Gaps = 9/249 (3%) Query: 258 VLEIKDLNIKESRGSLKVKGLSLDVRAGEIVGVAGIDGNGQTELVKAITGLTKVDSGSIK 317 VLE++ + K G ++G++L + GE+ + G +G G++ L+K + G D G I+ Sbjct: 18 VLEMQGI-AKRFHGVPALQGVNLTIYPGEVHALMGENGAGKSTLMKILAGAYIADEGEIR 76 Query: 318 LHNKDITNQRPRKITEQSVGHVPEDRHRDGLVLEMTVAENIALQTYYKPPMSKYGFLDYN 377 ++ K + P + + + ++ + + +TV ENI + + +++ FLD Sbjct: 77 INGKGVKITDPGTARQAGINLIYQELN---VAPNLTVTENIFMGS----ELTRGQFLDRK 129 Query: 378 KINSHARELMEEFDVRGAGEWVSASSLSGGNQQKAIIAREIDRNPDLLIVSQPTRGLDVG 437 + A++++ A + +L+ QQ+ IAR + N +L++ +PT L Sbjct: 130 AMELEAQQVLASLGASFAPTDI-VGTLAIAEQQQVEIARALKDNSRILVMDEPTAALSDR 188 Query: 438 AIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHDGQIQGIVSPETTTKQELGI 497 E + + + + R++G A++ IS ++EI ++DRI+V+ DGQ G ++ E + Q L Sbjct: 189 ETERLFEVIRKLRNDGIAIIYISHRMEEIYALADRISVLRDGQYIGSLTREEISPQRLVQ 248 Query: 498 LMVGGNINE 506 +MVG ++ + Sbjct: 249 MMVGRSMQD 257 Score = 76.6 bits (187), Expect = 2e-18 Identities = 60/217 (27%), Positives = 112/217 (51%), Gaps = 10/217 (4%) Query: 26 NLELKKGEIHALLGENGAGKSTLMNILSGLLEPSEGEVHVKGKLENIDSPSKAANLGIGM 85 + +L+ GEI L G GAG++ + ++ G GEV + GK I SPS A +GIG Sbjct: 287 SFQLRAGEILGLAGLVGAGRTEVSRLIFGADRKVSGEVFLNGKKLEIHSPSDAIAVGIGY 346 Query: 86 VHQHFMLVDAF---TVTENIILGNEVTKGINLDLK---TAKKKILELSERYGLSVEP-DA 138 V + F + +NI L N + + NL + + K + E + + + + Sbjct: 347 VPEDRKDQGLFLEMSSRKNIGL-NRLKQDANLGIVNWGSVNKIATDAVENFHIRLANLEI 405 Query: 139 LIRDISVGQQQRVEILKTLYRGADILIFDEPTAVLTPAEITELMQIMKNLIKEGKSIILI 198 D+S G QQ++ + + L +L+ DEPT + +E+ +I+ +L +G +I+++ Sbjct: 406 RAVDLSGGNQQKLLLARWLAINPRVLMLDEPTRGVDIGAKSEIYRIISDLSAQGVAILMV 465 Query: 199 THKLDEIRAVADRITVIRRGKSIDTVE--LGDKTNQE 233 + +L EI ++DR+ V+R G+ + ++ +G + QE Sbjct: 466 SSELPEIVGLSDRVLVMREGQLVGELDNSIGKEITQE 502 Lambda K H 0.315 0.135 0.365 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: 660 Number of extensions: 28 Number of successful extensions: 7 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 3 Length of query: 506 Length of database: 517 Length adjustment: 35 Effective length of query: 471 Effective length of database: 482 Effective search space: 227022 Effective search space used: 227022 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: 52 (24.6 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