Transporters, Polycystin cation channel, putative
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 9 |
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4I228
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 9 |
GO:0005216 | monoatomic ion channel activity | 4 | 9 |
GO:0005261 | monoatomic cation channel activity | 5 | 9 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 9 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 9 |
GO:0015267 | channel activity | 4 | 9 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 9 |
GO:0022803 | passive transmembrane transporter activity | 3 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 9 |
GO:0005217 | intracellular ligand-gated monoatomic ion channel activity | 6 | 1 |
GO:0005262 | calcium channel activity | 6 | 1 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 1 |
GO:0015276 | ligand-gated monoatomic ion channel activity | 5 | 1 |
GO:0015278 | calcium-release channel activity | 7 | 1 |
GO:0022834 | ligand-gated channel activity | 6 | 1 |
GO:0022836 | gated channel activity | 5 | 1 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 1 |
GO:0072345 | NAADP-sensitive calcium-release channel activity | 8 | 1 |
GO:0099094 | ligand-gated monoatomic cation channel activity | 6 | 1 |
GO:0099604 | ligand-gated calcium channel activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.341 |
CLV_MEL_PAP_1 | 164 | 170 | PF00089 | 0.606 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.518 |
CLV_PCSK_FUR_1 | 190 | 194 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.583 |
CLV_Separin_Metazoa | 571 | 575 | PF03568 | 0.664 |
DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.346 |
DEG_SPOP_SBC_1 | 499 | 503 | PF00917 | 0.639 |
DOC_ANK_TNKS_1 | 166 | 173 | PF00023 | 0.391 |
DOC_CYCLIN_RxL_1 | 79 | 89 | PF00134 | 0.395 |
DOC_MAPK_MEF2A_6 | 177 | 185 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 218 | 227 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 354 | 361 | PF00069 | 0.305 |
DOC_PP1_RVXF_1 | 180 | 186 | PF00149 | 0.271 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.373 |
DOC_USP7_MATH_2 | 528 | 534 | PF00917 | 0.622 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 167 | 175 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 35 | 39 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 531 | 537 | PF00244 | 0.807 |
LIG_14-3-3_CterR_2 | 587 | 590 | PF00244 | 0.677 |
LIG_Actin_WH2_2 | 168 | 184 | PF00022 | 0.371 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 302 | 307 | PF00928 | 0.540 |
LIG_EH1_1 | 352 | 360 | PF00400 | 0.389 |
LIG_EVH1_2 | 101 | 105 | PF00568 | 0.367 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.350 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.360 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.373 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.374 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.345 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.572 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.324 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.354 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.162 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.325 |
LIG_LIR_Gen_1 | 117 | 126 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 318 | 326 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.248 |
LIG_LIR_Gen_1 | 453 | 462 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 117 | 121 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 318 | 322 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 351 | 356 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.272 |
LIG_NRBOX | 12 | 18 | PF00104 | 0.331 |
LIG_Pex14_1 | 506 | 510 | PF04695 | 0.679 |
LIG_Pex14_2 | 446 | 450 | PF04695 | 0.272 |
LIG_Pex14_2 | 454 | 458 | PF04695 | 0.278 |
LIG_RPA_C_Fungi | 187 | 199 | PF08784 | 0.455 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.503 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.364 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.569 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.336 |
LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 36 | 40 | PF00017 | 0.412 |
LIG_SH2_NCK_1 | 75 | 79 | PF00017 | 0.395 |
LIG_SH2_PTP2 | 366 | 369 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 481 | 485 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.439 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.406 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.708 |
LIG_SUMO_SIM_anti_2 | 11 | 17 | PF11976 | 0.237 |
LIG_SUMO_SIM_anti_2 | 176 | 182 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 321 | 326 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 337 | 344 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 247 | 253 | PF11976 | 0.327 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.602 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.389 |
LIG_WRC_WIRS_1 | 316 | 321 | PF05994 | 0.331 |
LIG_WRC_WIRS_1 | 350 | 355 | PF05994 | 0.389 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.272 |
LIG_WRC_WIRS_1 | 451 | 456 | PF05994 | 0.272 |
MOD_CDK_SPK_2 | 565 | 570 | PF00069 | 0.746 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.580 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.429 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.341 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.314 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.521 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.756 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.698 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.518 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.406 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.613 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.641 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.460 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.733 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.431 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.452 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.434 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.331 |
MOD_GlcNHglycan | 512 | 516 | PF01048 | 0.571 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.635 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.496 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.585 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.502 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.404 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.266 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.332 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.539 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.428 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.457 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.686 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.719 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.506 |
MOD_LATS_1 | 328 | 334 | PF00433 | 0.340 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.381 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.480 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.460 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.237 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.523 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.582 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.361 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.313 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.239 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.314 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.484 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.293 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.246 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.321 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.438 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.389 |
MOD_PK_1 | 226 | 232 | PF00069 | 0.500 |
MOD_PKA_1 | 329 | 335 | PF00069 | 0.439 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.435 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.506 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.503 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.488 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.750 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.492 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.549 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.237 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.546 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.334 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.293 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.474 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.311 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.306 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.290 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.287 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.617 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.520 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.410 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.491 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.607 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.415 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.657 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.666 |
MOD_SUMO_rev_2 | 571 | 581 | PF00179 | 0.670 |
TRG_DiLeu_BaEn_1 | 338 | 343 | PF01217 | 0.389 |
TRG_DiLeu_LyEn_5 | 236 | 241 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.707 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.670 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.299 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.430 |
TRG_PTS1 | 587 | 590 | PF00515 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKU9 | Leptomonas seymouri | 59% | 97% |
A0A1X0NSA4 | Trypanosomatidae | 41% | 100% |
A0A3R7KKX3 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WZS8 | Leishmania donovani | 98% | 100% |
C9ZRX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AY77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q995 | Leishmania major | 92% | 100% |