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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4HFU5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0005215 | transporter activity | 1 | 5 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0022804 | active transmembrane transporter activity | 3 | 5 |
GO:0022857 | transmembrane transporter activity | 2 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 5 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0140359 | ABC-type transporter activity | 3 | 4 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.678 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.417 |
CLV_PCSK_FUR_1 | 166 | 170 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.432 |
DEG_APCC_DBOX_1 | 232 | 240 | PF00400 | 0.534 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.235 |
DOC_CYCLIN_RxL_1 | 350 | 357 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 252 | 258 | PF00134 | 0.506 |
DOC_MAPK_DCC_7 | 415 | 424 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 233 | 239 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 359 | 367 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 83 | 89 | PF00069 | 0.482 |
DOC_MAPK_HePTP_8 | 412 | 424 | PF00069 | 0.348 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 415 | 424 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 450 | 457 | PF00069 | 0.200 |
DOC_MAPK_MEF2A_6 | 482 | 489 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 499 | 507 | PF00069 | 0.228 |
DOC_MAPK_MEF2A_6 | 83 | 91 | PF00069 | 0.437 |
DOC_MAPK_NFAT4_5 | 234 | 242 | PF00069 | 0.448 |
DOC_MAPK_NFAT4_5 | 450 | 458 | PF00069 | 0.200 |
DOC_MAPK_NFAT4_5 | 84 | 92 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 448 | 455 | PF00149 | 0.154 |
DOC_PP1_RVXF_1 | 502 | 508 | PF00149 | 0.344 |
DOC_PP1_SILK_1 | 586 | 591 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.611 |
DOC_PP2B_LxvP_1 | 500 | 503 | PF13499 | 0.211 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.162 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.299 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.212 |
DOC_USP7_UBL2_3 | 207 | 211 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 15 | 21 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 353 | 359 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 476 | 482 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 58 | 62 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 602 | 607 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 625 | 633 | PF00244 | 0.484 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 569 | 573 | PF00533 | 0.162 |
LIG_EH1_1 | 491 | 499 | PF00400 | 0.471 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.583 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.476 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.535 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.387 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.527 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.328 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.431 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.564 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.633 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.438 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.675 |
LIG_GBD_Chelix_1 | 426 | 434 | PF00786 | 0.286 |
LIG_HP1_1 | 247 | 251 | PF01393 | 0.452 |
LIG_IRF3_LxIS_1 | 481 | 488 | PF10401 | 0.483 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 380 | 387 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 553 | 562 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 570 | 580 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 671 | 678 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 553 | 557 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.174 |
LIG_MLH1_MIPbox_1 | 569 | 573 | PF16413 | 0.162 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.271 |
LIG_Pex14_1 | 548 | 552 | PF04695 | 0.491 |
LIG_PTB_Apo_2 | 357 | 364 | PF02174 | 0.483 |
LIG_PTB_Apo_2 | 556 | 563 | PF02174 | 0.258 |
LIG_PTB_Phospho_1 | 357 | 363 | PF10480 | 0.486 |
LIG_PTB_Phospho_1 | 556 | 562 | PF10480 | 0.258 |
LIG_SH2_CRK | 565 | 569 | PF00017 | 0.255 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.242 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.568 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.442 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.548 |
LIG_SH2_STAT3 | 363 | 366 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 638 | 641 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.180 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 643 | 646 | PF00017 | 0.246 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.586 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.440 |
LIG_SH3_5 | 550 | 554 | PF00018 | 0.457 |
LIG_SUMO_SIM_anti_2 | 246 | 254 | PF11976 | 0.555 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 335 | 342 | PF11976 | 0.570 |
LIG_SUMO_SIM_anti_2 | 526 | 531 | PF11976 | 0.211 |
LIG_SUMO_SIM_anti_2 | 553 | 559 | PF11976 | 0.508 |
LIG_SUMO_SIM_anti_2 | 657 | 663 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 246 | 254 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 433 | 439 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 523 | 528 | PF11976 | 0.358 |
LIG_SxIP_EBH_1 | 572 | 581 | PF03271 | 0.360 |
LIG_TYR_ITIM | 591 | 596 | PF00017 | 0.402 |
LIG_TYR_ITSM | 217 | 224 | PF00017 | 0.339 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.245 |
LIG_WRC_WIRS_1 | 533 | 538 | PF05994 | 0.334 |
LIG_WW_1 | 393 | 396 | PF00397 | 0.485 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.395 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.322 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.756 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.363 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.567 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.523 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.361 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.695 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.358 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.502 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.421 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.530 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.415 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.683 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.425 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.336 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.389 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.689 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.299 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.564 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.241 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.512 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.419 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.468 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.236 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.523 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.408 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.721 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.419 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.316 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.684 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.301 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.512 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.571 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.577 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.415 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.386 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.240 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.373 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.495 |
MOD_N-GLC_1 | 621 | 626 | PF02516 | 0.467 |
MOD_N-GLC_2 | 113 | 115 | PF02516 | 0.248 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.515 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.341 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.289 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.288 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.353 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.203 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.616 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.270 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.375 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.620 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.653 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.224 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.247 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.237 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.251 |
MOD_NEK2_2 | 354 | 359 | PF00069 | 0.384 |
MOD_NEK2_2 | 477 | 482 | PF00069 | 0.209 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.591 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.462 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.366 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.523 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.468 |
MOD_PKB_1 | 375 | 383 | PF00069 | 0.364 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.287 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.741 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.442 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.357 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.608 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.479 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.436 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.423 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.406 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.242 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.265 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.644 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.190 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.270 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.335 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.577 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.565 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 468 | 471 | PF00179 | 0.340 |
MOD_SUMO_rev_2 | 199 | 209 | PF00179 | 0.241 |
MOD_SUMO_rev_2 | 305 | 311 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.185 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 601 | 604 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I194 | Leptomonas seymouri | 54% | 83% |
A0A0S4IZ09 | Bodo saltans | 37% | 100% |
A0A0S4KMF6 | Bodo saltans | 24% | 85% |
A0A1X0P4K0 | Trypanosomatidae | 33% | 100% |
A0A3Q8IDI3 | Leishmania donovani | 77% | 100% |
A0A3R7MIF6 | Trypanosoma rangeli | 32% | 100% |
A4I2W2 | Leishmania infantum | 77% | 100% |
E9ADE9 | Leishmania major | 75% | 100% |
Q4GZT4 | Bos taurus | 22% | 100% |
Q8MIB3 | Sus scrofa | 22% | 100% |
V5B0X3 | Trypanosoma cruzi | 34% | 100% |
V5BLN9 | Trypanosoma cruzi | 24% | 99% |