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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4H972
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.728 |
CLV_PCSK_FUR_1 | 143 | 147 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.718 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.583 |
CLV_PCSK_PC7_1 | 201 | 207 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.794 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.548 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.517 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.672 |
DEG_SPOP_SBC_1 | 382 | 386 | PF00917 | 0.700 |
DOC_CKS1_1 | 535 | 540 | PF01111 | 0.498 |
DOC_CYCLIN_yCln2_LP_2 | 123 | 129 | PF00134 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 592 | 598 | PF00134 | 0.547 |
DOC_MAPK_DCC_7 | 254 | 263 | PF00069 | 0.733 |
DOC_MAPK_gen_1 | 19 | 27 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 91 | 99 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 254 | 263 | PF00069 | 0.733 |
DOC_MAPK_MEF2A_6 | 93 | 101 | PF00069 | 0.482 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.764 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.548 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.571 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.589 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.837 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.861 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 346 | 356 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 374 | 382 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 399 | 403 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 459 | 466 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 484 | 488 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 570 | 575 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 84 | 89 | PF00244 | 0.537 |
LIG_BIR_III_4 | 412 | 416 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 601 | 605 | PF00533 | 0.741 |
LIG_CSL_BTD_1 | 379 | 382 | PF09270 | 0.547 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.750 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.669 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.685 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.561 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.654 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.607 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.439 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.445 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.654 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.608 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.817 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.516 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.437 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.564 |
LIG_HP1_1 | 259 | 263 | PF01393 | 0.730 |
LIG_Integrin_isoDGR_2 | 196 | 198 | PF01839 | 0.588 |
LIG_LIR_Gen_1 | 114 | 125 | PF02991 | 0.751 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.550 |
LIG_NRBOX | 543 | 549 | PF00104 | 0.748 |
LIG_PDZ_Class_1 | 604 | 609 | PF00595 | 0.523 |
LIG_SH2_NCK_1 | 518 | 522 | PF00017 | 0.495 |
LIG_SH2_SRC | 286 | 289 | PF00017 | 0.793 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.710 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.778 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.781 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.653 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.527 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.802 |
LIG_SUMO_SIM_anti_2 | 119 | 124 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 384 | 392 | PF11976 | 0.536 |
LIG_TRAF2_1 | 488 | 491 | PF00917 | 0.716 |
MOD_CDK_SPxK_1 | 360 | 366 | PF00069 | 0.590 |
MOD_CDK_SPxxK_3 | 360 | 367 | PF00069 | 0.734 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.625 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.587 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.687 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.784 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.860 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.755 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.556 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.585 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.701 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.531 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.584 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.667 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.582 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.742 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.561 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.439 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.564 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.568 |
MOD_GlcNHglycan | 36 | 40 | PF01048 | 0.787 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.740 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.567 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.772 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.706 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.607 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.621 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.821 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.700 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.758 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.628 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.736 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.798 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.695 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.607 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.484 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.555 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.694 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.595 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.568 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.555 |
MOD_N-GLC_1 | 599 | 604 | PF02516 | 0.675 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.717 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.534 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.633 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.778 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.611 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.642 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.741 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.542 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.527 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.555 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.528 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.491 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.651 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.581 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.552 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.809 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.549 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.664 |
MOD_PKB_1 | 597 | 605 | PF00069 | 0.516 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.511 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.530 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.556 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.480 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.566 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.799 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.537 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.597 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.839 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.861 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.709 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.502 |
TRG_DiLeu_BaEn_1 | 543 | 548 | PF01217 | 0.747 |
TRG_DiLeu_BaEn_1 | 587 | 592 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.702 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 556 | 558 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 596 | 599 | PF00400 | 0.678 |
TRG_NES_CRM1_1 | 543 | 555 | PF08389 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 589 | 594 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WUL8 | Leishmania donovani | 55% | 100% |
A4HXJ4 | Leishmania infantum | 55% | 100% |
E9AR89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
Q4QE74 | Leishmania major | 54% | 99% |