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: E9AF70
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.748 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.560 |
CLV_PCSK_FUR_1 | 444 | 448 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 474 | 476 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 179 | 185 | PF00082 | 0.593 |
CLV_PCSK_PC7_1 | 376 | 382 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 443 | 449 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.627 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.625 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.457 |
DEG_SPOP_SBC_1 | 98 | 102 | PF00917 | 0.485 |
DOC_CKS1_1 | 13 | 18 | PF01111 | 0.440 |
DOC_CYCLIN_RxL_1 | 397 | 405 | PF00134 | 0.498 |
DOC_CYCLIN_yClb1_LxF_4 | 478 | 483 | PF00134 | 0.657 |
DOC_MAPK_DCC_7 | 185 | 195 | PF00069 | 0.798 |
DOC_MAPK_gen_1 | 187 | 195 | PF00069 | 0.704 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 474 | 483 | PF00069 | 0.642 |
DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.704 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 193 | 209 | PF00069 | 0.774 |
DOC_PP1_RVXF_1 | 478 | 484 | PF00149 | 0.657 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.433 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.432 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.461 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.674 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.545 |
DOC_USP7_UBL2_3 | 183 | 187 | PF12436 | 0.713 |
DOC_USP7_UBL2_3 | 221 | 225 | PF12436 | 0.706 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.632 |
DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.519 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.464 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 448 | 454 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.457 |
LIG_Actin_WH2_2 | 350 | 367 | PF00022 | 0.634 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.453 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.739 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.575 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.676 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.730 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.685 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.815 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.611 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.515 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.582 |
LIG_Integrin_RGD_1 | 296 | 298 | PF01839 | 0.616 |
LIG_LIR_Gen_1 | 27 | 38 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 452 | 461 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.558 |
LIG_MLH1_MIPbox_1 | 26 | 30 | PF16413 | 0.453 |
LIG_MYND_1 | 320 | 324 | PF01753 | 0.601 |
LIG_MYND_1 | 38 | 42 | PF01753 | 0.424 |
LIG_Pex14_2 | 120 | 124 | PF04695 | 0.590 |
LIG_REV1ctd_RIR_1 | 351 | 360 | PF16727 | 0.535 |
LIG_SH2_PTP2 | 390 | 393 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.552 |
LIG_SH2_STAT3 | 457 | 460 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.521 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.432 |
LIG_SUMO_SIM_anti_2 | 18 | 24 | PF11976 | 0.457 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.410 |
LIG_UBA3_1 | 114 | 122 | PF00899 | 0.722 |
LIG_WRC_WIRS_1 | 426 | 431 | PF05994 | 0.653 |
MOD_CDK_SPxxK_3 | 12 | 19 | PF00069 | 0.444 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.719 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.469 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.451 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.690 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.786 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.678 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.588 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.681 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.372 |
MOD_Cter_Amidation | 147 | 150 | PF01082 | 0.623 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.758 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.602 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.448 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.570 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.565 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.497 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.687 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.776 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.477 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.586 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.653 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.479 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.484 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.477 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.483 |
MOD_LATS_1 | 97 | 103 | PF00433 | 0.485 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.477 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.478 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.621 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.520 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.580 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.452 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.744 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.469 |
MOD_PK_1 | 24 | 30 | PF00069 | 0.453 |
MOD_PKA_1 | 355 | 361 | PF00069 | 0.533 |
MOD_PKA_1 | 463 | 469 | PF00069 | 0.469 |
MOD_PKA_1 | 61 | 67 | PF00069 | 0.483 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.808 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.662 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.588 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.483 |
MOD_PKB_1 | 447 | 455 | PF00069 | 0.708 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.479 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.476 |
MOD_Plk_2-3 | 415 | 421 | PF00069 | 0.682 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.453 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.636 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.654 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.501 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.441 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.469 |
MOD_SUMO_for_1 | 224 | 227 | PF00179 | 0.785 |
MOD_SUMO_rev_2 | 246 | 255 | PF00179 | 0.788 |
MOD_SUMO_rev_2 | 330 | 338 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.452 |
TRG_NLS_Bipartite_1 | 133 | 153 | PF00514 | 0.580 |
TRG_NLS_Bipartite_1 | 172 | 188 | PF00514 | 0.680 |
TRG_NLS_Bipartite_1 | 207 | 223 | PF00514 | 0.625 |
TRG_NLS_Bipartite_1 | 463 | 478 | PF00514 | 0.556 |
TRG_NLS_MonoCore_2 | 183 | 188 | PF00514 | 0.576 |
TRG_NLS_MonoCore_2 | 217 | 222 | PF00514 | 0.688 |
TRG_NLS_MonoExtC_3 | 124 | 129 | PF00514 | 0.665 |
TRG_NLS_MonoExtC_3 | 182 | 187 | PF00514 | 0.580 |
TRG_NLS_MonoExtC_3 | 206 | 211 | PF00514 | 0.621 |
TRG_NLS_MonoExtN_4 | 122 | 129 | PF00514 | 0.670 |
TRG_NLS_MonoExtN_4 | 183 | 188 | PF00514 | 0.602 |
TRG_NLS_MonoExtN_4 | 218 | 223 | PF00514 | 0.699 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 480 | 484 | PF00026 | 0.624 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P943 | Leptomonas seymouri | 64% | 100% |
A0A3S7X9B6 | Leishmania donovani | 93% | 100% |
A4HMS0 | Leishmania braziliensis | 80% | 100% |
A4IBF6 | Leishmania infantum | 93% | 100% |
E9B6C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |