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:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AKT0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.768 |
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.645 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.500 |
CLV_PCSK_FUR_1 | 64 | 68 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 596 | 598 | PF00082 | 0.346 |
CLV_PCSK_PC7_1 | 232 | 238 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.599 |
DEG_APCC_DBOX_1 | 498 | 506 | PF00400 | 0.570 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.576 |
DEG_ODPH_VHL_1 | 39 | 51 | PF01847 | 0.638 |
DEG_SCF_FBW7_1 | 98 | 105 | PF00400 | 0.733 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.816 |
DEG_SPOP_SBC_1 | 284 | 288 | PF00917 | 0.583 |
DEG_SPOP_SBC_1 | 445 | 449 | PF00917 | 0.542 |
DEG_SPOP_SBC_1 | 562 | 566 | PF00917 | 0.739 |
DOC_CKS1_1 | 569 | 574 | PF01111 | 0.715 |
DOC_CYCLIN_yCln2_LP_2 | 358 | 364 | PF00134 | 0.774 |
DOC_CYCLIN_yCln2_LP_2 | 504 | 510 | PF00134 | 0.764 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 499 | 506 | PF00069 | 0.706 |
DOC_MAPK_NFAT4_5 | 499 | 507 | PF00069 | 0.556 |
DOC_MAPK_RevD_3 | 49 | 65 | PF00069 | 0.789 |
DOC_PP1_RVXF_1 | 501 | 507 | PF00149 | 0.711 |
DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.797 |
DOC_PP1_RVXF_1 | 638 | 644 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.584 |
DOC_PP2B_LxvP_1 | 508 | 511 | PF13499 | 0.674 |
DOC_PP2B_LxvP_1 | 513 | 516 | PF13499 | 0.644 |
DOC_PP4_FxxP_1 | 506 | 509 | PF00568 | 0.768 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.792 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.730 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 150 | 155 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 162 | 166 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 311 | 321 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 367 | 372 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 430 | 436 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 46 | 50 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 561 | 569 | PF00244 | 0.632 |
LIG_APCC_ABBA_1 | 529 | 534 | PF00400 | 0.708 |
LIG_BIR_III_2 | 575 | 579 | PF00653 | 0.771 |
LIG_BRCT_BRCA1_1 | 202 | 206 | PF00533 | 0.636 |
LIG_BRCT_BRCA1_1 | 285 | 289 | PF00533 | 0.787 |
LIG_EVH1_1 | 506 | 510 | PF00568 | 0.691 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.685 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.785 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.483 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.531 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.654 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.523 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.755 |
LIG_Integrin_isoDGR_2 | 428 | 430 | PF01839 | 0.717 |
LIG_LIR_Apic_2 | 331 | 337 | PF02991 | 0.794 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.760 |
LIG_LIR_Gen_1 | 149 | 157 | PF02991 | 0.683 |
LIG_LIR_LC3C_4 | 42 | 45 | PF02991 | 0.222 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.762 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.549 |
LIG_PDZ_Class_1 | 660 | 665 | PF00595 | 0.701 |
LIG_Pex14_1 | 130 | 134 | PF04695 | 0.766 |
LIG_Pex14_1 | 30 | 34 | PF04695 | 0.411 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.674 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.840 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.757 |
LIG_SH2_NCK_1 | 656 | 660 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.772 |
LIG_SH2_STAP1 | 451 | 455 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 656 | 660 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.755 |
LIG_SH3_1 | 334 | 340 | PF00018 | 0.837 |
LIG_SH3_2 | 509 | 514 | PF14604 | 0.663 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.702 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.827 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.517 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.700 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.741 |
LIG_SUMO_SIM_anti_2 | 410 | 417 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 139 | 146 | PF11976 | 0.759 |
LIG_TRAF2_1 | 518 | 521 | PF00917 | 0.640 |
LIG_TRAF2_1 | 616 | 619 | PF00917 | 0.563 |
LIG_TRAF2_2 | 603 | 608 | PF00917 | 0.546 |
LIG_TRFH_1 | 506 | 510 | PF08558 | 0.758 |
LIG_UBA3_1 | 591 | 596 | PF00899 | 0.546 |
LIG_WRC_WIRS_1 | 190 | 195 | PF05994 | 0.667 |
MOD_CDK_SPK_2 | 576 | 581 | PF00069 | 0.753 |
MOD_CDK_SPxxK_3 | 574 | 581 | PF00069 | 0.760 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.741 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.767 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.685 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.677 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.725 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.724 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.709 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.697 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.784 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.797 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.593 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.717 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.716 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.603 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.854 |
MOD_CK2_1 | 613 | 619 | PF00069 | 0.602 |
MOD_Cter_Amidation | 234 | 237 | PF01082 | 0.615 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.565 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.591 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.549 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.527 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.546 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.571 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.561 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.411 |
MOD_GlcNHglycan | 538 | 542 | PF01048 | 0.482 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.607 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.453 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.555 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.703 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.595 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.670 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.526 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.751 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.743 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.791 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.772 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.628 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.797 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.546 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.514 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.578 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.399 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.737 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.673 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.483 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.760 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.733 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.524 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.522 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.738 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.574 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.655 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.672 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.688 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.766 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.815 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.690 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.560 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.600 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.400 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.619 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.372 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.530 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.692 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.796 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.483 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.616 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.678 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.816 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.717 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.702 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.763 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.502 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.659 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.671 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.537 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.552 |
MOD_Plk_1 | 634 | 640 | PF00069 | 0.530 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.747 |
MOD_Plk_2-3 | 608 | 614 | PF00069 | 0.546 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.623 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.720 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.683 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.688 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.700 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.389 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.764 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.389 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.452 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.800 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.814 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.737 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.771 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.394 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.706 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.792 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.673 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.733 |
TRG_DiLeu_BaEn_1 | 291 | 296 | PF01217 | 0.566 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 525 | 530 | PF01217 | 0.625 |
TRG_DiLeu_BaLyEn_6 | 493 | 498 | PF01217 | 0.760 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.793 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.681 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.716 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 643 | 646 | PF00400 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 597 | 602 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIV8 | Leptomonas seymouri | 50% | 100% |
A0A3S5H5Q9 | Leishmania donovani | 90% | 100% |
A4H4L7 | Leishmania braziliensis | 77% | 100% |
A4HSU3 | Leishmania infantum | 91% | 100% |
Q4QJ27 | Leishmania major | 88% | 99% |