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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4IBU9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 131 | 135 | PF00656 | 0.605 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.560 |
CLV_PCSK_FUR_1 | 309 | 313 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 109 | 111 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 307 | 313 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.526 |
DEG_APCC_DBOX_1 | 52 | 60 | PF00400 | 0.533 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.731 |
DEG_SCF_FBW7_1 | 224 | 231 | PF00400 | 0.592 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.571 |
DOC_CYCLIN_yCln2_LP_2 | 163 | 169 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.638 |
DOC_MAPK_MEF2A_6 | 109 | 116 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 48 | 56 | PF00069 | 0.638 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 95 | 103 | PF00069 | 0.559 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.523 |
DOC_PP4_FxxP_1 | 402 | 405 | PF00568 | 0.655 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.641 |
DOC_USP7_UBL2_3 | 258 | 262 | PF12436 | 0.580 |
DOC_USP7_UBL2_3 | 44 | 48 | PF12436 | 0.575 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 386 | 392 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 417 | 422 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.553 |
LIG_Actin_WH2_2 | 39 | 55 | PF00022 | 0.665 |
LIG_APCC_ABBA_1 | 291 | 296 | PF00400 | 0.537 |
LIG_BRCT_BRCA1_1 | 144 | 148 | PF00533 | 0.554 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.481 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.637 |
LIG_BRCT_BRCA1_2 | 89 | 95 | PF00533 | 0.680 |
LIG_deltaCOP1_diTrp_1 | 67 | 75 | PF00928 | 0.522 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.490 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.396 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.503 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.709 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.630 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.610 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.572 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.416 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.736 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.431 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.709 |
LIG_LIR_Apic_2 | 145 | 151 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 155 | 165 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 369 | 380 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.508 |
LIG_LYPXL_yS_3 | 205 | 208 | PF13949 | 0.429 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.391 |
LIG_PCNA_yPIPBox_3 | 29 | 37 | PF02747 | 0.578 |
LIG_PDZ_Class_1 | 417 | 422 | PF00595 | 0.716 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.500 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.463 |
LIG_SH2_GRB2like | 376 | 379 | PF00017 | 0.560 |
LIG_SH2_NCK_1 | 294 | 298 | PF00017 | 0.386 |
LIG_SH2_SRC | 294 | 297 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.683 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.679 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.707 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.520 |
LIG_SH3_2 | 330 | 335 | PF14604 | 0.521 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.467 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.469 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.450 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 321 | 328 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 180 | 186 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 207 | 212 | PF11976 | 0.567 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.493 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.655 |
LIG_TRAF2_1 | 363 | 366 | PF00917 | 0.639 |
LIG_UBA3_1 | 384 | 392 | PF00899 | 0.453 |
LIG_WRC_WIRS_1 | 251 | 256 | PF05994 | 0.549 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.525 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.747 |
LIG_WW_3 | 328 | 332 | PF00397 | 0.535 |
MOD_CDC14_SPxK_1 | 328 | 331 | PF00782 | 0.535 |
MOD_CDK_SPxK_1 | 325 | 331 | PF00069 | 0.496 |
MOD_CDK_SPxxK_3 | 325 | 332 | PF00069 | 0.501 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.647 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.657 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.330 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.457 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.734 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.534 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.417 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.717 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.632 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.764 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.692 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.468 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.433 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.741 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.474 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.613 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.643 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.686 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.682 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.565 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.678 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.429 |
MOD_NEK2_2 | 333 | 338 | PF00069 | 0.523 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.607 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.567 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.461 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.679 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.450 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.535 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.596 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.634 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.580 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.579 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.715 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 377 | 385 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.438 |
TRG_DiLeu_BaEn_2 | 70 | 76 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_4 | 158 | 164 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 307 | 310 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.644 |
TRG_NLS_MonoExtC_3 | 217 | 222 | PF00514 | 0.637 |
TRG_NLS_MonoExtN_4 | 215 | 222 | PF00514 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 394 | 398 | PF00026 | 0.690 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBR9 | Leptomonas seymouri | 69% | 90% |
A0A0S4J059 | Bodo saltans | 44% | 94% |
A0A1X0P5E2 | Trypanosomatidae | 55% | 93% |
A0A3S7X9S4 | Leishmania donovani | 100% | 100% |
A4HN81 | Leishmania braziliensis | 86% | 100% |
C9ZYR2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 92% |
E9AFN6 | Leishmania major | 94% | 100% |
E9B6T9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BCS7 | Trypanosoma cruzi | 55% | 93% |