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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4H7L1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 13 |
GO:0005216 | monoatomic ion channel activity | 4 | 13 |
GO:0005227 | calcium activated cation channel activity | 6 | 13 |
GO:0005261 | monoatomic cation channel activity | 5 | 13 |
GO:0005267 | potassium channel activity | 6 | 13 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 13 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 13 |
GO:0015079 | potassium ion transmembrane transporter activity | 6 | 13 |
GO:0015267 | channel activity | 4 | 13 |
GO:0015269 | calcium-activated potassium channel activity | 7 | 13 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 13 |
GO:0016286 | small conductance calcium-activated potassium channel activity | 8 | 13 |
GO:0022803 | passive transmembrane transporter activity | 3 | 13 |
GO:0022836 | gated channel activity | 5 | 13 |
GO:0022839 | monoatomic ion gated channel activity | 6 | 13 |
GO:0022857 | transmembrane transporter activity | 2 | 13 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 13 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 13 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.304 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.377 |
CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.586 |
DEG_MDM2_SWIB_1 | 202 | 209 | PF02201 | 0.388 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.604 |
DEG_SCF_FBW7_1 | 370 | 377 | PF00400 | 0.715 |
DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.698 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.566 |
DOC_CYCLIN_yCln2_LP_2 | 274 | 280 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 313 | 324 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 117 | 126 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 316 | 324 | PF00069 | 0.621 |
DOC_MAPK_NFAT4_5 | 317 | 325 | PF00069 | 0.447 |
DOC_PP4_MxPP_1 | 128 | 131 | PF00568 | 0.394 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 248 | 255 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 335 | 340 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 399 | 405 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 448 | 456 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 494 | 503 | PF00244 | 0.725 |
LIG_Actin_WH2_2 | 357 | 373 | PF00022 | 0.623 |
LIG_Actin_WH2_2 | 444 | 459 | PF00022 | 0.592 |
LIG_APCC_ABBA_1 | 402 | 407 | PF00400 | 0.702 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.545 |
LIG_CaM_IQ_9 | 300 | 316 | PF13499 | 0.519 |
LIG_Clathr_ClatBox_1 | 30 | 34 | PF01394 | 0.624 |
LIG_CtBP_PxDLS_1 | 444 | 448 | PF00389 | 0.589 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.603 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.284 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.547 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.620 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.602 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.750 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.618 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.596 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.528 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 151 | 158 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 321 | 329 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.518 |
LIG_MYND_3 | 442 | 446 | PF01753 | 0.686 |
LIG_OCRL_FandH_1 | 178 | 190 | PF00620 | 0.461 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.304 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.448 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.310 |
LIG_SH2_SRC | 152 | 155 | PF00017 | 0.342 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.619 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.584 |
LIG_SUMO_SIM_par_1 | 271 | 276 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 29 | 34 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.294 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.248 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.327 |
MOD_CDK_SPK_2 | 389 | 394 | PF00069 | 0.698 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.617 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.253 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.607 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.529 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.639 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.707 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.700 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.251 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.551 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.704 |
MOD_Cter_Amidation | 397 | 400 | PF01082 | 0.465 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.534 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.394 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.426 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.501 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.637 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.304 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.562 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.601 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.654 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.661 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.610 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.604 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.688 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.737 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.637 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.665 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.582 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.437 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.304 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.187 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.539 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.498 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.596 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.722 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.783 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.605 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.297 |
MOD_NEK2_2 | 55 | 60 | PF00069 | 0.340 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.572 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.688 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.599 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.338 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.584 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.632 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.770 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.673 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.495 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.338 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.485 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.501 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.653 |
MOD_Plk_2-3 | 217 | 223 | PF00069 | 0.279 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.537 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.242 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.287 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.501 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.531 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.665 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.418 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.566 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.547 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.664 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.679 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.668 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.654 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.706 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.561 |
MOD_SUMO_for_1 | 312 | 315 | PF00179 | 0.535 |
MOD_SUMO_rev_2 | 401 | 410 | PF00179 | 0.673 |
TRG_DiLeu_BaEn_2 | 445 | 451 | PF01217 | 0.590 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.224 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.248 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.304 |
TRG_Pf-PMV_PEXEL_1 | 337 | 342 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3W7 | Leptomonas seymouri | 61% | 98% |
A0A0S4IWT9 | Bodo saltans | 30% | 95% |
A0A0S4IZM8 | Bodo saltans | 34% | 100% |
A0A1X0NNP7 | Trypanosomatidae | 29% | 94% |
A0A1X0NP80 | Trypanosomatidae | 36% | 100% |
A0A3Q8I9U0 | Leishmania donovani | 76% | 100% |
A0A422NNJ1 | Trypanosoma rangeli | 36% | 100% |
A4HVZ5 | Leishmania infantum | 76% | 100% |
E9APP7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QFT2 | Leishmania major | 76% | 100% |
V5BNC5 | Trypanosoma cruzi | 28% | 98% |