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: A4H8N3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.527 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.524 |
DEG_APCC_DBOX_1 | 295 | 303 | PF00400 | 0.437 |
DEG_SCF_TRCP1_1 | 168 | 174 | PF00400 | 0.719 |
DOC_CYCLIN_RxL_1 | 293 | 303 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 144 | 152 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 405 | 415 | PF00069 | 0.631 |
DOC_MAPK_MEF2A_6 | 119 | 126 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 408 | 417 | PF00069 | 0.546 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.501 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.721 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.502 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 222 | 226 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 45 | 52 | PF00244 | 0.656 |
LIG_Actin_WH2_2 | 428 | 444 | PF00022 | 0.443 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.600 |
LIG_CSL_BTD_1 | 87 | 90 | PF09270 | 0.521 |
LIG_eIF4E_1 | 482 | 488 | PF01652 | 0.432 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.635 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.690 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.569 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.514 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.677 |
LIG_LIR_Apic_2 | 381 | 385 | PF02991 | 0.521 |
LIG_LIR_Apic_2 | 479 | 485 | PF02991 | 0.656 |
LIG_LIR_Apic_2 | 84 | 90 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 242 | 252 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 424 | 428 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.711 |
LIG_LYPXL_S_1 | 189 | 193 | PF13949 | 0.511 |
LIG_LYPXL_yS_3 | 190 | 193 | PF13949 | 0.508 |
LIG_NRBOX | 342 | 348 | PF00104 | 0.470 |
LIG_PCNA_PIPBox_1 | 400 | 409 | PF02747 | 0.529 |
LIG_PCNA_yPIPBox_3 | 396 | 407 | PF02747 | 0.521 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.529 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.547 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.605 |
LIG_SH2_CRK | 407 | 411 | PF00017 | 0.500 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.598 |
LIG_SH2_NCK_1 | 382 | 386 | PF00017 | 0.560 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.679 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.508 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.730 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.692 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.611 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.611 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.568 |
LIG_TRFH_1 | 501 | 505 | PF08558 | 0.562 |
LIG_TYR_ITIM | 330 | 335 | PF00017 | 0.543 |
LIG_TYR_ITIM | 426 | 431 | PF00017 | 0.581 |
LIG_UBA3_1 | 142 | 147 | PF00899 | 0.597 |
LIG_UBA3_1 | 487 | 496 | PF00899 | 0.629 |
LIG_WRC_WIRS_1 | 422 | 427 | PF05994 | 0.357 |
MOD_CDK_SPxxK_3 | 194 | 201 | PF00069 | 0.519 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.551 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.705 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.582 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.554 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.684 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.573 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.671 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.537 |
MOD_CMANNOS | 387 | 390 | PF00535 | 0.631 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.539 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.449 |
MOD_GlcNHglycan | 167 | 171 | PF01048 | 0.708 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.635 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.621 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.475 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.588 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.642 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.671 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.744 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.720 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.637 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.519 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.733 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.691 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.597 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.537 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.669 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.568 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.464 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.721 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.687 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.488 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.720 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.603 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.503 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.435 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.757 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.725 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.654 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.534 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.502 |
MOD_NEK2_2 | 437 | 442 | PF00069 | 0.480 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.682 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.689 |
MOD_PK_1 | 248 | 254 | PF00069 | 0.496 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.557 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.458 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.713 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.559 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.599 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.608 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.591 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.771 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.555 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.759 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.425 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.681 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.488 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.600 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.392 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.546 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.587 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.745 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.570 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.496 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.693 |
MOD_SUMO_rev_2 | 359 | 367 | PF00179 | 0.651 |
TRG_DiLeu_BaEn_1 | 231 | 236 | PF01217 | 0.504 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.556 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 395 | 398 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 296 | 301 | PF00026 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM4 | Leptomonas seymouri | 69% | 100% |
A0A0S4KPP2 | Bodo saltans | 33% | 100% |
A0A1X0NYW7 | Trypanosomatidae | 44% | 100% |
A0A3S7WU15 | Leishmania donovani | 83% | 99% |
A0A422NAT9 | Trypanosoma rangeli | 44% | 100% |
A4HX03 | Leishmania infantum | 83% | 99% |
C9ZW04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AQR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QER0 | Leishmania major | 80% | 100% |