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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0005929 | cilium | 4 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
GO:0031514 | motile cilium | 5 | 1 |
Related structures:
AlphaFold database: A4HAH8
Term | Name | Level | Count |
---|---|---|---|
GO:0000281 | mitotic cytokinesis | 4 | 1 |
GO:0000910 | cytokinesis | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.736 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 809 | 811 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.532 |
CLV_PCSK_FUR_1 | 397 | 401 | PF00082 | 0.694 |
CLV_PCSK_FUR_1 | 528 | 532 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 811 | 813 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 236 | 238 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 530 | 532 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 811 | 813 | PF00082 | 0.458 |
CLV_PCSK_PC7_1 | 807 | 813 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 817 | 821 | PF00082 | 0.638 |
DEG_APCC_DBOX_1 | 110 | 118 | PF00400 | 0.419 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 727 | 735 | PF00400 | 0.458 |
DEG_APCC_DBOX_1 | 85 | 93 | PF00400 | 0.601 |
DEG_APCC_KENBOX_2 | 755 | 759 | PF00400 | 0.658 |
DEG_MDM2_SWIB_1 | 801 | 809 | PF02201 | 0.654 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.697 |
DOC_CKS1_1 | 559 | 564 | PF01111 | 0.604 |
DOC_MAPK_gen_1 | 672 | 680 | PF00069 | 0.664 |
DOC_MAPK_gen_1 | 737 | 744 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 283 | 292 | PF00069 | 0.460 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.606 |
DOC_USP7_UBL2_3 | 199 | 203 | PF12436 | 0.652 |
DOC_USP7_UBL2_3 | 312 | 316 | PF12436 | 0.436 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 123 | 131 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 351 | 361 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 385 | 391 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 407 | 411 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 423 | 432 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 538 | 542 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.424 |
LIG_Actin_WH2_2 | 110 | 125 | PF00022 | 0.620 |
LIG_Actin_WH2_2 | 357 | 375 | PF00022 | 0.419 |
LIG_CSK_EPIYA_1 | 458 | 462 | PF00017 | 0.710 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.464 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.719 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.470 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.577 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.470 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.418 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.653 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.506 |
LIG_FHA_1 | 781 | 787 | PF00498 | 0.717 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.650 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.601 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.552 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.610 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.437 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.539 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.609 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.589 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.724 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.572 |
LIG_GBD_Chelix_1 | 656 | 664 | PF00786 | 0.453 |
LIG_Integrin_isoDGR_2 | 72 | 74 | PF01839 | 0.574 |
LIG_LIR_Apic_2 | 780 | 785 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 41 | 47 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 631 | 639 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 704 | 713 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 77 | 85 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 794 | 801 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 802 | 813 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 704 | 709 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 794 | 800 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 802 | 808 | PF02991 | 0.617 |
LIG_LYPXL_SIV_4 | 224 | 232 | PF13949 | 0.577 |
LIG_PCNA_PIPBox_1 | 17 | 26 | PF02747 | 0.390 |
LIG_PCNA_PIPBox_1 | 177 | 186 | PF02747 | 0.417 |
LIG_PCNA_yPIPBox_3 | 14 | 24 | PF02747 | 0.393 |
LIG_Pex14_2 | 797 | 801 | PF04695 | 0.544 |
LIG_Pex14_2 | 840 | 844 | PF04695 | 0.498 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.448 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.612 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.571 |
LIG_SH2_CRK | 559 | 563 | PF00017 | 0.605 |
LIG_SH2_CRK | 706 | 710 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 559 | 563 | PF00017 | 0.605 |
LIG_SH2_PTP2 | 5 | 8 | PF00017 | 0.590 |
LIG_SH2_SRC | 23 | 26 | PF00017 | 0.578 |
LIG_SH2_SRC | 5 | 8 | PF00017 | 0.668 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 353 | 357 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.734 |
LIG_SH2_STAP1 | 706 | 710 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.558 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.606 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.492 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.519 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.722 |
LIG_SUMO_SIM_par_1 | 297 | 303 | PF11976 | 0.429 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.411 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.565 |
LIG_TRAF2_1 | 603 | 606 | PF00917 | 0.671 |
LIG_TRAF2_2 | 578 | 583 | PF00917 | 0.589 |
LIG_TYR_ITIM | 19 | 24 | PF00017 | 0.531 |
LIG_TYR_ITSM | 39 | 46 | PF00017 | 0.430 |
LIG_UBA3_1 | 81 | 88 | PF00899 | 0.561 |
LIG_WRC_WIRS_1 | 278 | 283 | PF05994 | 0.615 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.608 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.708 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.429 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.593 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.712 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.607 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.430 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.532 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.608 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.675 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.461 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.724 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.581 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.466 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.539 |
MOD_Cter_Amidation | 670 | 673 | PF01082 | 0.465 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.630 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.537 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.539 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.460 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.621 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.475 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.546 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.372 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.436 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.789 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.762 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.603 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.611 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.549 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.649 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.604 |
MOD_N-GLC_2 | 826 | 828 | PF02516 | 0.670 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.610 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.630 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.672 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.503 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.439 |
MOD_NEK2_1 | 821 | 826 | PF00069 | 0.452 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.836 |
MOD_PIKK_1 | 787 | 793 | PF00454 | 0.574 |
MOD_PK_1 | 88 | 94 | PF00069 | 0.608 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.630 |
MOD_PKA_1 | 423 | 429 | PF00069 | 0.645 |
MOD_PKA_1 | 672 | 678 | PF00069 | 0.474 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.611 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.593 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.546 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.475 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.662 |
MOD_PKA_2 | 795 | 801 | PF00069 | 0.699 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.620 |
MOD_PKB_1 | 423 | 431 | PF00069 | 0.646 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.581 |
MOD_Plk_2-3 | 415 | 421 | PF00069 | 0.623 |
MOD_Plk_2-3 | 490 | 496 | PF00069 | 0.468 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.404 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.611 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.609 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.524 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.521 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.644 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.638 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.551 |
MOD_SUMO_for_1 | 262 | 265 | PF00179 | 0.625 |
MOD_SUMO_for_1 | 519 | 522 | PF00179 | 0.539 |
MOD_SUMO_for_1 | 701 | 704 | PF00179 | 0.439 |
MOD_SUMO_rev_2 | 313 | 318 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 466 | 470 | PF00179 | 0.705 |
MOD_SUMO_rev_2 | 502 | 508 | PF00179 | 0.629 |
MOD_SUMO_rev_2 | 521 | 527 | PF00179 | 0.359 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_1 | 705 | 710 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_1 | 715 | 720 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_2 | 357 | 363 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 706 | 709 | PF00928 | 0.637 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.623 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 647 | 650 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 809 | 812 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.523 |
TRG_NES_CRM1_1 | 690 | 705 | PF08389 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7W0 | Leishmania donovani | 75% | 100% |
A4I9N8 | Leishmania infantum | 77% | 66% |
Q4Q3D9 | Leishmania major | 77% | 66% |