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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A0A3S7WRU9
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0005215 | transporter activity | 1 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0022804 | active transmembrane transporter activity | 3 | 6 |
GO:0022857 | transmembrane transporter activity | 2 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140359 | ABC-type transporter activity | 3 | 6 |
GO:0140657 | ATP-dependent activity | 1 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.369 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 349 | 351 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.349 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.577 |
DOC_ANK_TNKS_1 | 594 | 601 | PF00023 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 270 | 276 | PF00134 | 0.349 |
DOC_MAPK_gen_1 | 479 | 488 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 25 | 33 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 479 | 488 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 357 | 364 | PF00149 | 0.486 |
DOC_PP4_FxxP_1 | 158 | 161 | PF00568 | 0.493 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.525 |
DOC_USP7_UBL2_3 | 556 | 560 | PF12436 | 0.566 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 479 | 485 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 572 | 581 | PF00244 | 0.563 |
LIG_AP2alpha_1 | 613 | 617 | PF02296 | 0.576 |
LIG_APCC_ABBA_1 | 69 | 74 | PF00400 | 0.493 |
LIG_APCC_ABBAyCdc20_2 | 68 | 74 | PF00400 | 0.493 |
LIG_BIR_III_2 | 308 | 312 | PF00653 | 0.589 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.367 |
LIG_Clathr_ClatBox_1 | 249 | 253 | PF01394 | 0.349 |
LIG_Clathr_ClatBox_1 | 429 | 433 | PF01394 | 0.549 |
LIG_EH1_1 | 138 | 146 | PF00400 | 0.338 |
LIG_eIF4E_1 | 139 | 145 | PF01652 | 0.349 |
LIG_eIF4E_1 | 183 | 189 | PF01652 | 0.349 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.589 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.327 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.367 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.656 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.549 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.354 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.544 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.493 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.550 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.580 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.506 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.493 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.493 |
LIG_GBD_Chelix_1 | 205 | 213 | PF00786 | 0.381 |
LIG_LIR_Apic_2 | 157 | 161 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 70 | 75 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 133 | 141 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 362 | 371 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 48 | 58 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 580 | 590 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 615 | 622 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 123 | 127 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 449 | 453 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 580 | 585 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 642 | 647 | PF02991 | 0.666 |
LIG_NRBOX | 245 | 251 | PF00104 | 0.349 |
LIG_Pex14_1 | 128 | 132 | PF04695 | 0.306 |
LIG_Pex14_1 | 272 | 276 | PF04695 | 0.426 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.306 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.639 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.367 |
LIG_Pex14_2 | 53 | 57 | PF04695 | 0.493 |
LIG_Pex14_2 | 563 | 567 | PF04695 | 0.565 |
LIG_Pex14_2 | 613 | 617 | PF04695 | 0.576 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.660 |
LIG_SH2_CRK | 439 | 443 | PF00017 | 0.506 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.623 |
LIG_SH2_NCK_1 | 404 | 408 | PF00017 | 0.493 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.349 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 419 | 422 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.617 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.349 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.307 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.451 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.508 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.349 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.349 |
LIG_SUMO_SIM_anti_2 | 426 | 431 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 540 | 546 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 215 | 220 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 248 | 254 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 424 | 431 | PF11976 | 0.503 |
LIG_TRAF2_1 | 431 | 434 | PF00917 | 0.506 |
LIG_TRFH_1 | 234 | 238 | PF08558 | 0.349 |
LIG_TYR_ITIM | 274 | 279 | PF00017 | 0.349 |
LIG_UBA3_1 | 246 | 255 | PF00899 | 0.349 |
LIG_WRC_WIRS_1 | 54 | 59 | PF05994 | 0.493 |
LIG_WRC_WIRS_1 | 582 | 587 | PF05994 | 0.549 |
LIG_WRC_WIRS_1 | 644 | 649 | PF05994 | 0.604 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.344 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.493 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.621 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.587 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.506 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.493 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.579 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.572 |
MOD_Cter_Amidation | 599 | 602 | PF01082 | 0.414 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.576 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.496 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.311 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.314 |
MOD_GlcNHglycan | 498 | 503 | PF01048 | 0.306 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.344 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.320 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.293 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.420 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.287 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.292 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.440 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.667 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.474 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.531 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.546 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.548 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.391 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.550 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.277 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.352 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.463 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.375 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.501 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.605 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.464 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.354 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.546 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.548 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.618 |
MOD_NEK2_2 | 120 | 125 | PF00069 | 0.293 |
MOD_NEK2_2 | 461 | 466 | PF00069 | 0.493 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.581 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.546 |
MOD_PK_1 | 480 | 486 | PF00069 | 0.506 |
MOD_PKA_1 | 480 | 486 | PF00069 | 0.506 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.611 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.549 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.463 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.640 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.293 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.493 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.486 |
MOD_Plk_1 | 567 | 573 | PF00069 | 0.562 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.610 |
MOD_Plk_2-3 | 428 | 434 | PF00069 | 0.506 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.396 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.154 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.307 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.412 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.240 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.453 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.489 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.549 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.449 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_1 | 449 | 454 | PF01217 | 0.493 |
TRG_DiLeu_BaEn_1 | 599 | 604 | PF01217 | 0.611 |
TRG_DiLeu_BaEn_2 | 368 | 374 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_4 | 433 | 439 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_4 | 533 | 539 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 270 | 275 | PF01217 | 0.349 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.665 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.658 |
TRG_NES_CRM1_1 | 268 | 280 | PF08389 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 114 | 118 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 601 | 606 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4KM38 | Bodo saltans | 47% | 98% |
A0A3S5H6J8 | Leishmania donovani | 100% | 100% |
A4HV30 | Leishmania infantum | 100% | 100% |
E9AYZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
Q1PEH6 | Arabidopsis thaliana | 26% | 71% |
Q552P3 | Dictyostelium discoideum | 28% | 79% |
Q84K47 | Arabidopsis thaliana | 28% | 67% |
Q8LPK0 | Arabidopsis thaliana | 25% | 73% |
Q8T6J0 | Dictyostelium discoideum | 28% | 78% |
Q9FLT4 | Arabidopsis thaliana | 28% | 72% |
Q9FLT8 | Arabidopsis thaliana | 27% | 72% |
Q9STT6 | Arabidopsis thaliana | 27% | 71% |
Q9STT7 | Arabidopsis thaliana | 27% | 70% |
Q9STT8 | Arabidopsis thaliana | 27% | 70% |
V5BQS2 | Trypanosoma cruzi | 24% | 100% |