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: Q4Q5M5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.805 |
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.816 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.821 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.489 |
CLV_PCSK_FUR_1 | 378 | 382 | PF00082 | 0.755 |
CLV_PCSK_FUR_1 | 87 | 91 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.832 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 549 | 551 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 476 | 478 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 549 | 551 | PF00082 | 0.735 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.496 |
CLV_PCSK_PC7_1 | 378 | 384 | PF00082 | 0.737 |
CLV_PCSK_PC7_1 | 472 | 478 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.749 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.834 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.834 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.514 |
DOC_MAPK_MEF2A_6 | 485 | 494 | PF00069 | 0.678 |
DOC_PP4_MxPP_1 | 123 | 126 | PF00568 | 0.663 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.768 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.653 |
DOC_USP7_UBL2_3 | 474 | 478 | PF12436 | 0.749 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.760 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 356 | 364 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 78 | 83 | PF00244 | 0.524 |
LIG_Actin_WH2_2 | 64 | 80 | PF00022 | 0.620 |
LIG_BIR_III_2 | 153 | 157 | PF00653 | 0.626 |
LIG_BRCT_BRCA1_1 | 266 | 270 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.647 |
LIG_deltaCOP1_diTrp_1 | 33 | 42 | PF00928 | 0.494 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.481 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.456 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.517 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.559 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.733 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.596 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.714 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.710 |
LIG_Integrin_RGD_1 | 383 | 385 | PF01839 | 0.629 |
LIG_LIR_Apic_2 | 249 | 255 | PF02991 | 0.776 |
LIG_LIR_Apic_2 | 282 | 288 | PF02991 | 0.576 |
LIG_LIR_Apic_2 | 497 | 503 | PF02991 | 0.686 |
LIG_LIR_Gen_1 | 271 | 278 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 51 | 59 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 95 | 106 | PF02991 | 0.496 |
LIG_LIR_LC3C_4 | 349 | 354 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.497 |
LIG_LYPXL_S_1 | 43 | 47 | PF13949 | 0.486 |
LIG_LYPXL_yS_3 | 44 | 47 | PF13949 | 0.499 |
LIG_PDZ_Class_3 | 581 | 586 | PF00595 | 0.640 |
LIG_Pex14_1 | 272 | 276 | PF04695 | 0.513 |
LIG_PTAP_UEV_1 | 155 | 160 | PF05743 | 0.698 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.766 |
LIG_SH2_CRK | 500 | 504 | PF00017 | 0.675 |
LIG_SH2_NCK_1 | 500 | 504 | PF00017 | 0.675 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.473 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.607 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.818 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.532 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.538 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 349 | 355 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 148 | 153 | PF11976 | 0.712 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.563 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.492 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.704 |
LIG_TYR_ITSM | 94 | 101 | PF00017 | 0.479 |
LIG_WW_3 | 126 | 130 | PF00397 | 0.704 |
MOD_CDK_SPxK_1 | 241 | 247 | PF00069 | 0.730 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.822 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.751 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.671 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.782 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.759 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.716 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.709 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.770 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.731 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.740 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.653 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.717 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.796 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.521 |
MOD_Cter_Amidation | 87 | 90 | PF01082 | 0.602 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.784 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.751 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.746 |
MOD_GlcNHglycan | 200 | 206 | PF01048 | 0.804 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.746 |
MOD_GlcNHglycan | 324 | 328 | PF01048 | 0.571 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.671 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.814 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.757 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.541 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.609 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.825 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.827 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.721 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.723 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.693 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.537 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.622 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.718 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.575 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.564 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.495 |
MOD_LATS_1 | 227 | 233 | PF00433 | 0.757 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.602 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.545 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.523 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.632 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.720 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.527 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.560 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.672 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.781 |
MOD_PKA_1 | 258 | 264 | PF00069 | 0.643 |
MOD_PKA_1 | 549 | 555 | PF00069 | 0.737 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.686 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.525 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.597 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.624 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.724 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.674 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.639 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.495 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.602 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.646 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.538 |
MOD_Plk_2-3 | 405 | 411 | PF00069 | 0.800 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.788 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.495 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.792 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.796 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.576 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.619 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.646 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.506 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.754 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.820 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.730 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.801 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.752 |
MOD_SUMO_for_1 | 117 | 120 | PF00179 | 0.571 |
MOD_SUMO_for_1 | 514 | 517 | PF00179 | 0.730 |
MOD_SUMO_rev_2 | 104 | 109 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 139 | 149 | PF00179 | 0.832 |
MOD_SUMO_rev_2 | 163 | 172 | PF00179 | 0.760 |
MOD_SUMO_rev_2 | 33 | 38 | PF00179 | 0.612 |
TRG_DiLeu_BaEn_4 | 104 | 110 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.832 |
TRG_NES_CRM1_1 | 108 | 120 | PF08389 | 0.630 |
TRG_NLS_MonoCore_2 | 450 | 455 | PF00514 | 0.763 |
TRG_NLS_MonoCore_2 | 88 | 93 | PF00514 | 0.488 |
TRG_NLS_MonoExtC_3 | 450 | 456 | PF00514 | 0.731 |
TRG_NLS_MonoExtN_4 | 546 | 553 | PF00514 | 0.817 |
TRG_NLS_MonoExtN_4 | 87 | 93 | PF00514 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.640 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1J1 | Leptomonas seymouri | 53% | 99% |
A0A3S5H7R3 | Leishmania donovani | 94% | 100% |
A4HK39 | Leishmania braziliensis | 76% | 100% |
A4I7M4 | Leishmania infantum | 94% | 100% |
E9B2I1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |