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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4HFI7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.356 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.601 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.410 |
CLV_PCSK_PC7_1 | 375 | 381 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.338 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.369 |
DOC_CYCLIN_RxL_1 | 39 | 49 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 325 | 333 | PF00069 | 0.553 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.561 |
DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.689 |
DOC_USP7_UBL2_3 | 321 | 325 | PF12436 | 0.601 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 181 | 188 | PF00244 | 0.444 |
LIG_APCC_ABBA_1 | 366 | 371 | PF00400 | 0.328 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.375 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.338 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.673 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.333 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.502 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.579 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 3 | 7 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.392 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.513 |
LIG_PCNA_TLS_4 | 294 | 301 | PF02747 | 0.336 |
LIG_PDZ_Class_2 | 462 | 467 | PF00595 | 0.584 |
LIG_Rb_LxCxE_1 | 25 | 47 | PF01857 | 0.314 |
LIG_RPA_C_Fungi | 365 | 377 | PF08784 | 0.544 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.491 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.477 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.644 |
LIG_SH2_STAT3 | 300 | 303 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 37 | 40 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.483 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.555 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.419 |
LIG_SUMO_SIM_par_1 | 455 | 461 | PF11976 | 0.486 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.494 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.589 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.497 |
LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.464 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.316 |
LIG_ULM_U2AF65_1 | 239 | 244 | PF00076 | 0.677 |
MOD_CDC14_SPxK_1 | 20 | 23 | PF00782 | 0.689 |
MOD_CDK_SPK_2 | 17 | 22 | PF00069 | 0.509 |
MOD_CDK_SPxK_1 | 17 | 23 | PF00069 | 0.663 |
MOD_CDK_SPxxK_3 | 17 | 24 | PF00069 | 0.631 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.704 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.762 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.697 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.564 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.603 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.576 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.544 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.571 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.572 |
MOD_Cter_Amidation | 13 | 16 | PF01082 | 0.504 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.682 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.646 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.504 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.641 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.489 |
MOD_N-GLC_2 | 437 | 439 | PF02516 | 0.482 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.530 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.327 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.281 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.584 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.496 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.709 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.468 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.682 |
MOD_PKA_1 | 325 | 331 | PF00069 | 0.334 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.653 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.588 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.402 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.691 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.607 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.334 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.410 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.371 |
MOD_Plk_2-3 | 210 | 216 | PF00069 | 0.544 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.589 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.737 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.697 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.557 |
MOD_SUMO_for_1 | 245 | 248 | PF00179 | 0.692 |
MOD_SUMO_for_1 | 414 | 417 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 139 | 145 | PF00179 | 0.516 |
MOD_SUMO_rev_2 | 227 | 232 | PF00179 | 0.701 |
MOD_SUMO_rev_2 | 262 | 269 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 287 | 295 | PF00179 | 0.508 |
TRG_DiLeu_BaEn_4 | 124 | 130 | PF01217 | 0.354 |
TRG_DiLeu_BaEn_4 | 292 | 298 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_4 | 73 | 79 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.356 |
TRG_NLS_Bipartite_1 | 224 | 243 | PF00514 | 0.450 |
TRG_NLS_MonoExtN_4 | 236 | 243 | PF00514 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.710 |
TRG_Pf-PMV_PEXEL_1 | 282 | 286 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILN1 | Leptomonas seymouri | 58% | 100% |
A0A1X0P3Z6 | Trypanosomatidae | 32% | 100% |
A0A3Q8IE88 | Leishmania donovani | 74% | 100% |
A0A3R7MQZ8 | Trypanosoma rangeli | 30% | 100% |
D0A5R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AD38 | Leishmania major | 73% | 99% |
E9AHD1 | Leishmania infantum | 74% | 100% |
E9AYW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
V5BE50 | Trypanosoma cruzi | 28% | 100% |