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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: Q4QFW3
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005543 | phospholipid binding | 3 | 12 |
GO:0008289 | lipid binding | 2 | 12 |
GO:0035091 | phosphatidylinositol binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.738 |
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.689 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.429 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.448 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 160 | 166 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.327 |
CLV_Separin_Metazoa | 429 | 433 | PF03568 | 0.488 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.522 |
DEG_COP1_1 | 19 | 27 | PF00400 | 0.525 |
DEG_MDM2_SWIB_1 | 226 | 233 | PF02201 | 0.594 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.672 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.751 |
DOC_CYCLIN_RxL_1 | 381 | 389 | PF00134 | 0.499 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 103 | 110 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 326 | 333 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 56 | 64 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 332 | 338 | PF00149 | 0.400 |
DOC_PP4_FxxP_1 | 130 | 133 | PF00568 | 0.391 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.599 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.437 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.665 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 153 | 158 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 138 | 155 | PF00022 | 0.532 |
LIG_Actin_WH2_2 | 244 | 261 | PF00022 | 0.559 |
LIG_Actin_WH2_2 | 265 | 283 | PF00022 | 0.569 |
LIG_Actin_WH2_2 | 417 | 434 | PF00022 | 0.504 |
LIG_BIR_III_4 | 300 | 304 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.699 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.448 |
LIG_CaM_IQ_9 | 418 | 434 | PF13499 | 0.504 |
LIG_deltaCOP1_diTrp_1 | 124 | 130 | PF00928 | 0.448 |
LIG_eIF4E_1 | 70 | 76 | PF01652 | 0.470 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.526 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.420 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.516 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.543 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.546 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.575 |
LIG_LIR_Apic_2 | 123 | 128 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 19 | 25 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 69 | 73 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 325 | 335 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 436 | 446 | PF02991 | 0.686 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 168 | 172 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.311 |
LIG_NRBOX | 63 | 69 | PF00104 | 0.412 |
LIG_Pex14_1 | 125 | 129 | PF04695 | 0.448 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.440 |
LIG_Pex14_2 | 226 | 230 | PF04695 | 0.608 |
LIG_REV1ctd_RIR_1 | 190 | 200 | PF16727 | 0.642 |
LIG_REV1ctd_RIR_1 | 394 | 405 | PF16727 | 0.471 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.477 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 328 | 331 | PF00017 | 0.529 |
LIG_SH2_NCK_1 | 439 | 443 | PF00017 | 0.420 |
LIG_SH2_SRC | 232 | 235 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 378 | 382 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.217 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.448 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.761 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.465 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.586 |
LIG_SUMO_SIM_anti_2 | 347 | 353 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 59 | 66 | PF11976 | 0.470 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.596 |
LIG_TRFH_1 | 129 | 133 | PF08558 | 0.468 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.529 |
LIG_UBA3_1 | 76 | 83 | PF00899 | 0.412 |
MOD_CDK_SPxxK_3 | 75 | 82 | PF00069 | 0.470 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.637 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.519 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.576 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.547 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.437 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.670 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.587 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.634 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.392 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.668 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.541 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.527 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.547 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.366 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.448 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.588 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.670 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.410 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.539 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.584 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.362 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.416 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.647 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.470 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.308 |
MOD_N-GLC_2 | 330 | 332 | PF02516 | 0.515 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.551 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.471 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.506 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.560 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.528 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.484 |
MOD_NEK2_2 | 289 | 294 | PF00069 | 0.527 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.545 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.492 |
MOD_PK_1 | 82 | 88 | PF00069 | 0.448 |
MOD_PKA_1 | 56 | 62 | PF00069 | 0.327 |
MOD_PKA_1 | 82 | 88 | PF00069 | 0.448 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.454 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.327 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.437 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.672 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.561 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.547 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.544 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.534 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.589 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.561 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.340 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.270 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.534 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.680 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.470 |
MOD_SUMO_rev_2 | 320 | 329 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_1 | 138 | 143 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.509 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 384 | 389 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 403 | 408 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW83 | Leptomonas seymouri | 73% | 78% |
A0A0S4IZJ1 | Bodo saltans | 26% | 81% |
A0A1X0NNT5 | Trypanosomatidae | 30% | 80% |
A0A3R7LA20 | Trypanosoma rangeli | 30% | 92% |
A0A3S7WSS9 | Leishmania donovani | 98% | 100% |
A4H7I2 | Leishmania braziliensis | 91% | 100% |
A4HVW4 | Leishmania infantum | 98% | 100% |
C9ZT62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 86% |
E9APL5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5BMA1 | Trypanosoma cruzi | 30% | 91% |