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 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A0A3S5H5Q9
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 | 0.760 |
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 552 | 556 | PF00656 | 0.747 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.484 |
CLV_PCSK_FUR_1 | 64 | 68 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 592 | 594 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.579 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.552 |
DEG_ODPH_VHL_1 | 39 | 51 | PF01847 | 0.699 |
DEG_ODPH_VHL_1 | 459 | 472 | PF01847 | 0.509 |
DEG_SCF_FBW7_1 | 98 | 105 | PF00400 | 0.729 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.806 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.543 |
DEG_SPOP_SBC_1 | 558 | 562 | PF00917 | 0.763 |
DOC_CKS1_1 | 565 | 570 | PF01111 | 0.706 |
DOC_CYCLIN_yCln2_LP_2 | 360 | 366 | PF00134 | 0.778 |
DOC_CYCLIN_yCln2_LP_2 | 506 | 512 | PF00134 | 0.761 |
DOC_MAPK_gen_1 | 501 | 508 | PF00069 | 0.682 |
DOC_MAPK_MEF2A_6 | 284 | 291 | PF00069 | 0.637 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.695 |
DOC_MAPK_MEF2A_6 | 501 | 508 | PF00069 | 0.709 |
DOC_MAPK_NFAT4_5 | 284 | 292 | PF00069 | 0.636 |
DOC_MAPK_RevD_3 | 49 | 65 | PF00069 | 0.775 |
DOC_PP1_RVXF_1 | 503 | 509 | PF00149 | 0.712 |
DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.781 |
DOC_PP1_RVXF_1 | 634 | 640 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 510 | 513 | PF13499 | 0.664 |
DOC_PP2B_LxvP_1 | 515 | 518 | PF13499 | 0.634 |
DOC_PP4_FxxP_1 | 508 | 511 | PF00568 | 0.763 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.791 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 164 | 168 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 369 | 374 | PF00244 | 0.750 |
LIG_14-3-3_CanoR_1 | 393 | 397 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 444 | 453 | PF00244 | 0.552 |
LIG_APCC_ABBA_1 | 531 | 536 | PF00400 | 0.702 |
LIG_BIR_III_2 | 571 | 575 | PF00653 | 0.757 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.636 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.785 |
LIG_EVH1_1 | 508 | 512 | PF00568 | 0.685 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.679 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.690 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.777 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.488 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.529 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.646 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.523 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.526 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.772 |
LIG_GBD_Chelix_1 | 43 | 51 | PF00786 | 0.493 |
LIG_Integrin_isoDGR_2 | 179 | 181 | PF01839 | 0.489 |
LIG_Integrin_isoDGR_2 | 430 | 432 | PF01839 | 0.717 |
LIG_LIR_Apic_2 | 333 | 339 | PF02991 | 0.785 |
LIG_LIR_Apic_2 | 395 | 400 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.761 |
LIG_LIR_Gen_1 | 151 | 159 | PF02991 | 0.679 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.762 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 586 | 591 | PF02991 | 0.549 |
LIG_PDZ_Class_1 | 656 | 661 | PF00595 | 0.690 |
LIG_Pex14_1 | 132 | 136 | PF04695 | 0.765 |
LIG_Pex14_1 | 30 | 34 | PF04695 | 0.411 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.678 |
LIG_SH2_CRK | 336 | 340 | PF00017 | 0.833 |
LIG_SH2_NCK_1 | 652 | 656 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.771 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 652 | 656 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.743 |
LIG_SH3_1 | 336 | 342 | PF00018 | 0.829 |
LIG_SH3_2 | 511 | 516 | PF14604 | 0.654 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.705 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.819 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.510 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.340 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.697 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.736 |
LIG_SUMO_SIM_anti_2 | 139 | 145 | PF11976 | 0.734 |
LIG_SUMO_SIM_anti_2 | 412 | 419 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 141 | 148 | PF11976 | 0.763 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.634 |
LIG_TRAF2_1 | 612 | 615 | PF00917 | 0.563 |
LIG_TRAF2_2 | 599 | 604 | PF00917 | 0.546 |
LIG_TRFH_1 | 508 | 512 | PF08558 | 0.752 |
LIG_UBA3_1 | 587 | 592 | PF00899 | 0.546 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.677 |
MOD_CDK_SPK_2 | 364 | 369 | PF00069 | 0.749 |
MOD_CDK_SPK_2 | 572 | 577 | PF00069 | 0.739 |
MOD_CDK_SPxxK_3 | 570 | 577 | PF00069 | 0.747 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.763 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.687 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.679 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.720 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.728 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.694 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.776 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.597 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.596 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.722 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.730 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.674 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.599 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.847 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.602 |
MOD_Cter_Amidation | 236 | 239 | PF01082 | 0.611 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.585 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.560 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.523 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.542 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.461 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.569 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.562 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.411 |
MOD_GlcNHglycan | 540 | 544 | PF01048 | 0.480 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.595 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.449 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.548 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.729 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.702 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.591 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.677 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.524 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.746 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.785 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.510 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.764 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.630 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.551 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.583 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.721 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.483 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.759 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.729 |
MOD_N-GLC_1 | 631 | 636 | PF02516 | 0.266 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.523 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.738 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.654 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.677 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.686 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.768 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.805 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.689 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.555 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.400 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.372 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.718 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.530 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.685 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.482 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.785 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.678 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.815 |
MOD_PKA_1 | 238 | 244 | PF00069 | 0.769 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.718 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.696 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.732 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.381 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.501 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.664 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.537 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.747 |
MOD_Plk_1 | 630 | 636 | PF00069 | 0.530 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.743 |
MOD_Plk_2-3 | 604 | 610 | PF00069 | 0.546 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.724 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.688 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.692 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.699 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.687 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.389 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.442 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.773 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.676 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.680 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.796 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.807 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.729 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.778 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.700 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.783 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.661 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.728 |
TRG_DiLeu_BaEn_1 | 527 | 532 | PF01217 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 495 | 500 | PF01217 | 0.757 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.778 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.676 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 639 | 642 | PF00400 | 0.563 |
TRG_ER_FFAT_2 | 399 | 408 | PF00635 | 0.454 |
TRG_NES_CRM1_1 | 309 | 322 | PF08389 | 0.706 |
TRG_Pf-PMV_PEXEL_1 | 593 | 598 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIV8 | Leptomonas seymouri | 50% | 100% |
A4H4L7 | Leishmania braziliensis | 78% | 100% |
A4HSU3 | Leishmania infantum | 99% | 100% |
E9AKT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QJ27 | Leishmania major | 93% | 100% |