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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0005929 | cilium | 4 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036038 | MKS complex | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IB52
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0030030 | cell projection organization | 4 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 199 | 203 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 392 | 396 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 445 | 447 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.542 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.450 |
DEG_APCC_DBOX_1 | 354 | 362 | PF00400 | 0.631 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.635 |
DEG_SPOP_SBC_1 | 384 | 388 | PF00917 | 0.696 |
DEG_SPOP_SBC_1 | 496 | 500 | PF00917 | 0.547 |
DOC_ANK_TNKS_1 | 176 | 183 | PF00023 | 0.524 |
DOC_CDC14_PxL_1 | 99 | 107 | PF14671 | 0.560 |
DOC_CKS1_1 | 586 | 591 | PF01111 | 0.416 |
DOC_CYCLIN_RxL_1 | 13 | 24 | PF00134 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 146 | 152 | PF00134 | 0.610 |
DOC_CYCLIN_yCln2_LP_2 | 438 | 444 | PF00134 | 0.623 |
DOC_CYCLIN_yCln2_LP_2 | 565 | 571 | PF00134 | 0.547 |
DOC_MAPK_gen_1 | 11 | 18 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 17 | 24 | PF00149 | 0.370 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.609 |
DOC_PP2B_LxvP_1 | 565 | 568 | PF13499 | 0.547 |
DOC_PP4_FxxP_1 | 120 | 123 | PF00568 | 0.378 |
DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.471 |
DOC_PP4_FxxP_1 | 539 | 542 | PF00568 | 0.471 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.547 |
DOC_USP7_MATH_2 | 55 | 61 | PF00917 | 0.507 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 286 | 290 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 602 | 606 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 87 | 92 | PF00244 | 0.661 |
LIG_Actin_WH2_2 | 344 | 361 | PF00022 | 0.629 |
LIG_APCC_ABBA_1 | 59 | 64 | PF00400 | 0.477 |
LIG_APCC_ABBAyCdc20_2 | 631 | 637 | PF00400 | 0.514 |
LIG_Clathr_ClatBox_1 | 524 | 528 | PF01394 | 0.547 |
LIG_deltaCOP1_diTrp_1 | 472 | 476 | PF00928 | 0.547 |
LIG_DLG_GKlike_1 | 430 | 438 | PF00625 | 0.690 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.422 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.500 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.439 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.368 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.483 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.557 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.455 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.508 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.487 |
LIG_LIR_Apic_2 | 528 | 534 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 536 | 542 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 341 | 351 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 455 | 464 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 472 | 481 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 503 | 513 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 472 | 476 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 503 | 509 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.486 |
LIG_NBox_RRM_1 | 23 | 33 | PF00076 | 0.482 |
LIG_PCNA_TLS_4 | 122 | 129 | PF02747 | 0.514 |
LIG_Pex14_2 | 531 | 535 | PF04695 | 0.471 |
LIG_PTB_Apo_2 | 529 | 536 | PF02174 | 0.493 |
LIG_REV1ctd_RIR_1 | 116 | 122 | PF16727 | 0.379 |
LIG_REV1ctd_RIR_1 | 260 | 266 | PF16727 | 0.518 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.452 |
LIG_SH2_CRK | 571 | 575 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 571 | 575 | PF00017 | 0.514 |
LIG_SH2_SRC | 635 | 638 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 635 | 639 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.243 |
LIG_SH3_2 | 545 | 550 | PF14604 | 0.514 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.595 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.571 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.446 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.506 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.514 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.514 |
LIG_SUMO_SIM_par_1 | 522 | 528 | PF11976 | 0.514 |
LIG_TYR_ITIM | 569 | 574 | PF00017 | 0.514 |
LIG_WRC_WIRS_1 | 282 | 287 | PF05994 | 0.365 |
MOD_CDC14_SPxK_1 | 547 | 550 | PF00782 | 0.514 |
MOD_CDK_SPxK_1 | 544 | 550 | PF00069 | 0.514 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.683 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.700 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.706 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.525 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.485 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.521 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.719 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.492 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.703 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.668 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.388 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.487 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.608 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.768 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.690 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.405 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.680 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.618 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.714 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.550 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.700 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.686 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.468 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.432 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.371 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.659 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.780 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.481 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.561 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.514 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.633 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.513 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.497 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.506 |
MOD_N-GLC_2 | 162 | 164 | PF02516 | 0.547 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.392 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.293 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.398 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.637 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.631 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.563 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.503 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.519 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.546 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.471 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.520 |
MOD_NEK2_2 | 207 | 212 | PF00069 | 0.610 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.479 |
MOD_NEK2_2 | 471 | 476 | PF00069 | 0.484 |
MOD_NEK2_2 | 513 | 518 | PF00069 | 0.422 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.706 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.471 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.510 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.545 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.425 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.491 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.732 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.505 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.543 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.606 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.596 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.465 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.483 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.471 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.514 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.493 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.613 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.439 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.515 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.511 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.506 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.561 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.667 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.793 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.643 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.640 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.579 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.388 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.514 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.514 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.514 |
MOD_SUMO_rev_2 | 34 | 38 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 43 | 53 | PF00179 | 0.377 |
TRG_DiLeu_BaEn_1 | 520 | 525 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_2 | 471 | 477 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 547 | 552 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 355 | 357 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.623 |
TRG_NES_CRM1_1 | 522 | 536 | PF08389 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 355 | 360 | PF00026 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7B5 | Leptomonas seymouri | 53% | 100% |
A0A0S4IRB4 | Bodo saltans | 27% | 82% |
A4I0K7 | Leishmania infantum | 100% | 100% |
E9AWG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QB03 | Leishmania major | 90% | 100% |