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: E9AVT2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.750 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.773 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.773 |
CLV_PCSK_PC1ET2_1 | 318 | 320 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.519 |
DEG_SPOP_SBC_1 | 102 | 106 | PF00917 | 0.677 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.735 |
DEG_SPOP_SBC_1 | 75 | 79 | PF00917 | 0.615 |
DOC_CDC14_PxL_1 | 536 | 544 | PF14671 | 0.336 |
DOC_CKS1_1 | 65 | 70 | PF01111 | 0.727 |
DOC_CYCLIN_RxL_1 | 441 | 450 | PF00134 | 0.520 |
DOC_MAPK_MEF2A_6 | 580 | 587 | PF00069 | 0.644 |
DOC_PP2B_PxIxI_1 | 438 | 444 | PF00149 | 0.550 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.729 |
DOC_SPAK_OSR1_1 | 580 | 584 | PF12202 | 0.569 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.731 |
LIG_14-3-3_CanoR_1 | 197 | 205 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 293 | 299 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 400 | 408 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 484 | 490 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 508 | 517 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 54 | 61 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 495 | 512 | PF00022 | 0.530 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.624 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.661 |
LIG_CSL_BTD_1 | 534 | 537 | PF09270 | 0.519 |
LIG_deltaCOP1_diTrp_1 | 6 | 12 | PF00928 | 0.596 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.579 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.574 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.372 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.678 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.654 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.617 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.468 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.761 |
LIG_HP1_1 | 325 | 329 | PF01393 | 0.599 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 194 | 201 | PF02991 | 0.665 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 432 | 443 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 559 | 569 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 10 | 15 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.524 |
LIG_MAD2 | 38 | 46 | PF02301 | 0.746 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.575 |
LIG_PDZ_Class_2 | 582 | 587 | PF00595 | 0.541 |
LIG_Pex14_1 | 8 | 12 | PF04695 | 0.546 |
LIG_RPA_C_Fungi | 253 | 265 | PF08784 | 0.590 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.642 |
LIG_SH2_NCK_1 | 547 | 551 | PF00017 | 0.631 |
LIG_SH2_NCK_1 | 562 | 566 | PF00017 | 0.389 |
LIG_SH2_PTP2 | 435 | 438 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 401 | 405 | PF00017 | 0.502 |
LIG_SH2_STAT3 | 292 | 295 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.545 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.629 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.665 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.655 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.681 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.433 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.573 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.601 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.730 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.549 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.764 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.500 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.759 |
LIG_SUMO_SIM_par_1 | 342 | 349 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 444 | 450 | PF11976 | 0.540 |
LIG_SUMO_SIM_par_1 | 528 | 533 | PF11976 | 0.511 |
LIG_TYR_ITIM | 560 | 565 | PF00017 | 0.633 |
MOD_CDC14_SPxK_1 | 149 | 152 | PF00782 | 0.618 |
MOD_CDK_SPxK_1 | 146 | 152 | PF00069 | 0.752 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.741 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.693 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.646 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.811 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.665 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.703 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.684 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.719 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.685 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.664 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.473 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.519 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.653 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.585 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.760 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.740 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.698 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.564 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.649 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.677 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.576 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.560 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.651 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.606 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.745 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.739 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.613 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.752 |
MOD_GlcNHglycan | 470 | 474 | PF01048 | 0.560 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.537 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.621 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.702 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.734 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.691 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.720 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.662 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.634 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.697 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.625 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.506 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.570 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.663 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.711 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.332 |
MOD_N-GLC_1 | 462 | 467 | PF02516 | 0.552 |
MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.686 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.581 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.728 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.542 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.470 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.766 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.598 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.537 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.482 |
MOD_NEK2_2 | 439 | 444 | PF00069 | 0.524 |
MOD_NEK2_2 | 556 | 561 | PF00069 | 0.501 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.768 |
MOD_PK_1 | 359 | 365 | PF00069 | 0.616 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.697 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.730 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.589 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.583 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.601 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.405 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.534 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.713 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.648 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.570 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.381 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.453 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.471 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.578 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.619 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.695 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.542 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.707 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.605 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.518 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.291 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.487 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.355 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.646 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.771 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.707 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.677 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.705 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.715 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.570 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.468 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.729 |
TRG_DiLeu_BaLyEn_6 | 441 | 446 | PF01217 | 0.618 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.713 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.681 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.770 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.536 |
TRG_NES_CRM1_1 | 493 | 507 | PF08389 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 13 | 18 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 444 | 449 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA8 | Leptomonas seymouri | 49% | 100% |
A0A3Q8IEA0 | Leishmania donovani | 86% | 100% |
A4HCC4 | Leishmania braziliensis | 75% | 99% |
A4HZX3 | Leishmania infantum | 87% | 100% |
Q4QBP7 | Leishmania major | 87% | 100% |