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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q4S5
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.815 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.461 |
CLV_PCSK_FUR_1 | 377 | 381 | PF00082 | 0.589 |
CLV_PCSK_FUR_1 | 382 | 386 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.575 |
CLV_PCSK_PC7_1 | 380 | 386 | PF00082 | 0.666 |
CLV_PCSK_PC7_1 | 390 | 396 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.564 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.550 |
DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.566 |
DEG_COP1_1 | 448 | 457 | PF00400 | 0.562 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.600 |
DOC_CDC14_PxL_1 | 17 | 25 | PF14671 | 0.678 |
DOC_CKS1_1 | 115 | 120 | PF01111 | 0.705 |
DOC_CYCLIN_RxL_1 | 194 | 205 | PF00134 | 0.692 |
DOC_CYCLIN_yCln2_LP_2 | 155 | 158 | PF00134 | 0.618 |
DOC_MAPK_gen_1 | 390 | 400 | PF00069 | 0.685 |
DOC_MAPK_MEF2A_6 | 312 | 319 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 393 | 402 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 195 | 202 | PF00149 | 0.690 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.763 |
DOC_PP2B_PxIxI_1 | 454 | 460 | PF00149 | 0.280 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.679 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.554 |
DOC_USP7_UBL2_3 | 414 | 418 | PF12436 | 0.575 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 485 | 489 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 502 | 507 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 522 | 527 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.652 |
LIG_BRCT_BRCA1_1 | 491 | 495 | PF00533 | 0.546 |
LIG_DLG_GKlike_1 | 522 | 530 | PF00625 | 0.660 |
LIG_eIF4E_1 | 521 | 527 | PF01652 | 0.594 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.521 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.531 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.513 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.497 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.590 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.530 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.671 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.660 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.543 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.531 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.459 |
LIG_FHA_2 | 558 | 564 | PF00498 | 0.655 |
LIG_IBAR_NPY_1 | 240 | 242 | PF08397 | 0.528 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.609 |
LIG_NRBOX | 470 | 476 | PF00104 | 0.546 |
LIG_PCNA_PIPBox_1 | 81 | 90 | PF02747 | 0.670 |
LIG_PDZ_Class_2 | 562 | 567 | PF00595 | 0.537 |
LIG_PDZ_Wminus1_1 | 565 | 567 | PF00595 | 0.565 |
LIG_PTB_Apo_2 | 237 | 244 | PF02174 | 0.510 |
LIG_PTB_Apo_2 | 515 | 522 | PF02174 | 0.619 |
LIG_PTB_Phospho_1 | 515 | 521 | PF10480 | 0.619 |
LIG_Rb_pABgroove_1 | 18 | 26 | PF01858 | 0.597 |
LIG_REV1ctd_RIR_1 | 198 | 203 | PF16727 | 0.578 |
LIG_RPA_C_Fungi | 373 | 385 | PF08784 | 0.571 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.707 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.411 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.464 |
LIG_SH2_NCK_1 | 524 | 528 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.564 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.782 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.739 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 533 | 539 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 291 | 298 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 50 | 55 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 536 | 542 | PF11976 | 0.543 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.773 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.411 |
MOD_CDK_SPxK_1 | 135 | 141 | PF00069 | 0.746 |
MOD_CDK_SPxxK_3 | 171 | 178 | PF00069 | 0.806 |
MOD_CDK_SPxxK_3 | 249 | 256 | PF00069 | 0.503 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.650 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.718 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.553 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.661 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.706 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.641 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.713 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.720 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.552 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.682 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.806 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.537 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.693 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.397 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.387 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.619 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.613 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.734 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.826 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.796 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.640 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.694 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.467 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.794 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.811 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.615 |
MOD_GlcNHglycan | 489 | 494 | PF01048 | 0.411 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.422 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.715 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.687 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.639 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.633 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.702 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.680 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.583 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.680 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.715 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.357 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.620 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.700 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.617 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.555 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.460 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.555 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.420 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.695 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.694 |
MOD_PK_1 | 393 | 399 | PF00069 | 0.692 |
MOD_PK_1 | 502 | 508 | PF00069 | 0.474 |
MOD_PK_1 | 547 | 553 | PF00069 | 0.543 |
MOD_PKA_1 | 393 | 399 | PF00069 | 0.692 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.824 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.703 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.692 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.411 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.688 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.540 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.573 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.475 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.486 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.696 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.498 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.715 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.692 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.522 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.693 |
MOD_SUMO_rev_2 | 406 | 416 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_4 | 507 | 513 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.634 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.613 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 382 | 385 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 74 | 76 | PF00400 | 0.461 |
TRG_NLS_Bipartite_1 | 376 | 397 | PF00514 | 0.583 |
TRG_NLS_MonoExtC_3 | 377 | 382 | PF00514 | 0.599 |
TRG_NLS_MonoExtN_4 | 376 | 383 | PF00514 | 0.588 |
TRG_NLS_MonoExtN_4 | 390 | 397 | PF00514 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAT8 | Leptomonas seymouri | 53% | 100% |
A0A3Q8IDF9 | Leishmania donovani | 93% | 100% |
A4HKZ0 | Leishmania braziliensis | 77% | 100% |
A4I8H1 | Leishmania infantum | 92% | 100% |
E9B3D1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |