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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HK39
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.370 |
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.631 |
CLV_PCSK_FUR_1 | 377 | 381 | PF00082 | 0.636 |
CLV_PCSK_FUR_1 | 87 | 91 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 541 | 543 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.381 |
CLV_PCSK_PC7_1 | 223 | 229 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.836 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.431 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.528 |
DOC_PP4_MxPP_1 | 123 | 126 | PF00568 | 0.541 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.521 |
DOC_USP7_UBL2_3 | 446 | 450 | PF12436 | 0.642 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.736 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 347 | 351 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 355 | 363 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 78 | 83 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 64 | 80 | PF00022 | 0.500 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 482 | 486 | PF00533 | 0.599 |
LIG_deltaCOP1_diTrp_1 | 33 | 42 | PF00928 | 0.403 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.383 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.445 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.487 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.618 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.606 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.611 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.544 |
LIG_LIR_Apic_2 | 248 | 254 | PF02991 | 0.728 |
LIG_LIR_Apic_2 | 281 | 287 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 51 | 59 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 95 | 106 | PF02991 | 0.393 |
LIG_LIR_LC3C_4 | 348 | 353 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.433 |
LIG_LYPXL_S_1 | 43 | 47 | PF13949 | 0.389 |
LIG_LYPXL_yS_3 | 44 | 47 | PF13949 | 0.402 |
LIG_PDZ_Class_3 | 573 | 578 | PF00595 | 0.542 |
LIG_PDZ_Wminus1_1 | 576 | 578 | PF00595 | 0.472 |
LIG_Pex14_1 | 271 | 275 | PF04695 | 0.418 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.408 |
LIG_SH3_1 | 122 | 128 | PF00018 | 0.462 |
LIG_SH3_2 | 156 | 161 | PF14604 | 0.538 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.548 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.692 |
LIG_SH3_3 | 491 | 497 | PF00018 | 0.495 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.516 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 348 | 354 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 148 | 155 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 348 | 354 | PF11976 | 0.478 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.391 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.525 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.597 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.550 |
LIG_WW_3 | 126 | 130 | PF00397 | 0.582 |
LIG_WW_3 | 224 | 228 | PF00397 | 0.544 |
MOD_CDC14_SPxK_1 | 158 | 161 | PF00782 | 0.543 |
MOD_CDK_SPxK_1 | 155 | 161 | PF00069 | 0.539 |
MOD_CDK_SPxK_1 | 240 | 246 | PF00069 | 0.636 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.730 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.586 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.718 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.665 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.629 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.639 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.623 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.604 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.403 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.603 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.683 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.544 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.494 |
MOD_Cter_Amidation | 87 | 90 | PF01082 | 0.472 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.688 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.659 |
MOD_GlcNHglycan | 199 | 205 | PF01048 | 0.692 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.815 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.580 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.526 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.734 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.646 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.523 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.471 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.554 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.687 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.524 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.638 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.830 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.430 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.471 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.557 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.599 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.542 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.534 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.513 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.481 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.518 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.435 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.510 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.426 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.598 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.636 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.427 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.490 |
MOD_PIKK_1 | 418 | 424 | PF00454 | 0.625 |
MOD_PK_1 | 327 | 333 | PF00069 | 0.403 |
MOD_PKA_1 | 232 | 238 | PF00069 | 0.560 |
MOD_PKA_1 | 541 | 547 | PF00069 | 0.625 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.685 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.596 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.429 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.505 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.543 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.599 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.621 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.533 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.420 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.543 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.534 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.479 |
MOD_Plk_2-3 | 385 | 391 | PF00069 | 0.518 |
MOD_Plk_2-3 | 405 | 411 | PF00069 | 0.602 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.666 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.420 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.602 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.756 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.622 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.485 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.525 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.534 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.441 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.695 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.659 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.735 |
MOD_SUMO_for_1 | 117 | 120 | PF00179 | 0.465 |
MOD_SUMO_rev_2 | 104 | 109 | PF00179 | 0.390 |
MOD_SUMO_rev_2 | 139 | 149 | PF00179 | 0.686 |
MOD_SUMO_rev_2 | 33 | 38 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_4 | 104 | 110 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_4 | 145 | 151 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.644 |
TRG_ER_diLys_1 | 574 | 578 | PF00400 | 0.491 |
TRG_NES_CRM1_1 | 108 | 120 | PF08389 | 0.502 |
TRG_NLS_MonoExtC_3 | 358 | 363 | PF00514 | 0.501 |
TRG_NLS_MonoExtN_4 | 538 | 545 | PF00514 | 0.684 |
TRG_NLS_MonoExtN_4 | 87 | 93 | PF00514 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1J1 | Leptomonas seymouri | 53% | 98% |
A0A3S5H7R3 | Leishmania donovani | 77% | 98% |
A4I7M4 | Leishmania infantum | 76% | 98% |
E9B2I1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |
Q4Q5M5 | Leishmania major | 76% | 100% |