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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AI99
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.559 |
CLV_PCSK_FUR_1 | 342 | 346 | PF00082 | 0.663 |
CLV_PCSK_FUR_1 | 560 | 564 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 559 | 561 | PF00082 | 0.650 |
CLV_PCSK_PC7_1 | 257 | 263 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.670 |
DOC_CYCLIN_RxL_1 | 290 | 300 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 342 | 350 | PF00069 | 0.671 |
DOC_PP1_RVXF_1 | 300 | 306 | PF00149 | 0.616 |
DOC_PP2B_LxvP_1 | 295 | 298 | PF13499 | 0.633 |
DOC_PP4_FxxP_1 | 433 | 436 | PF00568 | 0.683 |
DOC_PP4_FxxP_1 | 584 | 587 | PF00568 | 0.685 |
DOC_SPAK_OSR1_1 | 275 | 279 | PF12202 | 0.567 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.700 |
DOC_USP7_MATH_2 | 50 | 56 | PF00917 | 0.366 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.710 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.770 |
LIG_14-3-3_CanoR_1 | 523 | 531 | PF00244 | 0.639 |
LIG_APCC_ABBA_1 | 143 | 148 | PF00400 | 0.480 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 584 | 588 | PF00533 | 0.643 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.462 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.457 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.459 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.698 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.777 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.567 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.600 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.667 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.363 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.537 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.693 |
LIG_LIR_Apic_2 | 268 | 273 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 431 | 436 | PF02991 | 0.729 |
LIG_LIR_Apic_2 | 449 | 455 | PF02991 | 0.421 |
LIG_LIR_Apic_2 | 583 | 587 | PF02991 | 0.688 |
LIG_LIR_Gen_1 | 14 | 23 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 242 | 252 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 485 | 494 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 485 | 490 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.474 |
LIG_PCNA_yPIPBox_3 | 384 | 398 | PF02747 | 0.311 |
LIG_Pex14_1 | 452 | 456 | PF04695 | 0.715 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.436 |
LIG_Pex14_2 | 580 | 584 | PF04695 | 0.671 |
LIG_Rb_pABgroove_1 | 280 | 288 | PF01858 | 0.533 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.516 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 270 | 274 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.460 |
LIG_SH2_PTP2 | 111 | 114 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 245 | 248 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.712 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 511 | 514 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.453 |
LIG_SH3_2 | 337 | 342 | PF14604 | 0.411 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.617 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.567 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.503 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.718 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.518 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.677 |
LIG_SUMO_SIM_par_1 | 421 | 427 | PF11976 | 0.557 |
LIG_SUMO_SIM_par_1 | 502 | 508 | PF11976 | 0.606 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.632 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.543 |
LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.733 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.591 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.738 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.742 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.550 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.652 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.660 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.641 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.780 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.662 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.394 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.557 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.715 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.770 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.777 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.637 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.474 |
MOD_Cter_Amidation | 557 | 560 | PF01082 | 0.718 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.705 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.763 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.723 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.654 |
MOD_GlcNHglycan | 366 | 370 | PF01048 | 0.652 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.602 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.622 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.498 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.616 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.625 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.712 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.762 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.677 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.678 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.606 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.639 |
MOD_LATS_1 | 255 | 261 | PF00433 | 0.375 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.434 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.637 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.560 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.577 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.706 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.524 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.420 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.621 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.645 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.607 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.552 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.602 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.628 |
MOD_Plk_1 | 507 | 513 | PF00069 | 0.563 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.557 |
MOD_Plk_1 | 582 | 588 | PF00069 | 0.610 |
MOD_Plk_2-3 | 119 | 125 | PF00069 | 0.504 |
MOD_Plk_2-3 | 431 | 437 | PF00069 | 0.477 |
MOD_Plk_2-3 | 52 | 58 | PF00069 | 0.359 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.666 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.710 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.610 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.654 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.504 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.534 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.690 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.645 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.678 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.588 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.599 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.764 |
MOD_SUMO_for_1 | 383 | 386 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 171 | 181 | PF00179 | 0.695 |
TRG_DiLeu_BaEn_1 | 52 | 57 | PF01217 | 0.569 |
TRG_DiLeu_BaEn_2 | 17 | 23 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.713 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.540 |
TRG_NLS_MonoCore_2 | 558 | 563 | PF00514 | 0.681 |
TRG_NLS_MonoExtC_3 | 558 | 563 | PF00514 | 0.652 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC36 | Leptomonas seymouri | 53% | 95% |
A0A1X0NWG5 | Trypanosomatidae | 32% | 100% |
A0A3R7MIM2 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WVS1 | Leishmania donovani | 78% | 100% |
A4HYM7 | Leishmania infantum | 77% | 100% |
C9ZI60 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AUI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QD00 | Leishmania major | 79% | 96% |