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 |
Related structures:
AlphaFold database: E9B6K9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.585 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.815 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 587 | 589 | PF00082 | 0.815 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.451 |
DEG_APCC_DBOX_1 | 422 | 430 | PF00400 | 0.569 |
DEG_SPOP_SBC_1 | 577 | 581 | PF00917 | 0.821 |
DOC_CKS1_1 | 234 | 239 | PF01111 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 234 | 240 | PF00134 | 0.508 |
DOC_MAPK_DCC_7 | 423 | 431 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 423 | 432 | PF00069 | 0.577 |
DOC_MAPK_NFAT4_5 | 423 | 431 | PF00069 | 0.678 |
DOC_PP1_RVXF_1 | 432 | 439 | PF00149 | 0.526 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.821 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.671 |
DOC_USP7_UBL2_3 | 468 | 472 | PF12436 | 0.792 |
DOC_USP7_UBL2_3 | 630 | 634 | PF12436 | 0.666 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 142 | 152 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 387 | 396 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 487 | 496 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 56 | 66 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 597 | 603 | PF00244 | 0.584 |
LIG_Actin_WH2_2 | 419 | 435 | PF00022 | 0.654 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_EVH1_1 | 81 | 85 | PF00568 | 0.497 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.604 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.491 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.408 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.463 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.522 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.667 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.531 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.554 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.468 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.536 |
LIG_Integrin_isoDGR_2 | 572 | 574 | PF01839 | 0.747 |
LIG_LIR_Apic_2 | 226 | 230 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 532 | 543 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.517 |
LIG_LIR_LC3C_4 | 105 | 108 | PF02991 | 0.675 |
LIG_LIR_LC3C_4 | 236 | 241 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 324 | 330 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.535 |
LIG_PTAP_UEV_1 | 375 | 380 | PF05743 | 0.524 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.467 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.492 |
LIG_SH2_CRK | 535 | 539 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 499 | 503 | PF00017 | 0.619 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.598 |
LIG_SH2_SRC | 406 | 409 | PF00017 | 0.628 |
LIG_SH2_STAT3 | 132 | 135 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.494 |
LIG_SH3_2 | 156 | 161 | PF14604 | 0.501 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.500 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.787 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.747 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.586 |
LIG_SUMO_SIM_anti_2 | 235 | 242 | PF11976 | 0.603 |
LIG_SUMO_SIM_anti_2 | 338 | 344 | PF11976 | 0.612 |
LIG_SUMO_SIM_anti_2 | 514 | 520 | PF11976 | 0.627 |
LIG_SUMO_SIM_anti_2 | 623 | 632 | PF11976 | 0.701 |
LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.686 |
LIG_TYR_ITSM | 323 | 330 | PF00017 | 0.495 |
LIG_UBA3_1 | 428 | 434 | PF00899 | 0.535 |
LIG_WRC_WIRS_1 | 293 | 298 | PF05994 | 0.577 |
LIG_WRC_WIRS_1 | 567 | 572 | PF05994 | 0.736 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.657 |
MOD_CDK_SPxxK_3 | 392 | 399 | PF00069 | 0.396 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.480 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.615 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.627 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.667 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.723 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.623 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.646 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.506 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.720 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.685 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.586 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.615 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.706 |
MOD_Cter_Amidation | 477 | 480 | PF01082 | 0.522 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.417 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.616 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.460 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.543 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.634 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.570 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.629 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.745 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.575 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.772 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.711 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.693 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.548 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.612 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.594 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.585 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.621 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.462 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.695 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.771 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.618 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.699 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.775 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.632 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.713 |
MOD_N-GLC_2 | 446 | 448 | PF02516 | 0.521 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.491 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.638 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.640 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.671 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.726 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.426 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.678 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.665 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.474 |
MOD_NEK2_2 | 449 | 454 | PF00069 | 0.586 |
MOD_NEK2_2 | 7 | 12 | PF00069 | 0.669 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.730 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.563 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.442 |
MOD_PK_1 | 133 | 139 | PF00069 | 0.525 |
MOD_PKA_1 | 387 | 393 | PF00069 | 0.494 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.596 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.539 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.604 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.523 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.336 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.713 |
MOD_PKB_1 | 175 | 183 | PF00069 | 0.713 |
MOD_PKB_1 | 485 | 493 | PF00069 | 0.536 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.553 |
MOD_Plk_2-3 | 278 | 284 | PF00069 | 0.787 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.409 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.520 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.701 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.671 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.525 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.614 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.514 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.604 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.728 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.600 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.633 |
TRG_DiLeu_BaEn_1 | 425 | 430 | PF01217 | 0.675 |
TRG_DiLeu_BaEn_1 | 624 | 629 | PF01217 | 0.683 |
TRG_DiLeu_BaLyEn_6 | 234 | 239 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 424 | 429 | PF01217 | 0.559 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.707 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.527 |
TRG_NLS_MonoExtC_3 | 478 | 484 | PF00514 | 0.596 |
TRG_NLS_MonoExtN_4 | 476 | 483 | PF00514 | 0.596 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCD2 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IJ91 | Leishmania donovani | 86% | 100% |
A4HMZ7 | Leishmania braziliensis | 69% | 99% |
A4IBM0 | Leishmania infantum | 86% | 100% |
E9AFF4 | Leishmania major | 87% | 100% |