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: E9AYW2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.656 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.645 |
CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.585 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.389 |
DEG_SPOP_SBC_1 | 8 | 12 | PF00917 | 0.477 |
DOC_CYCLIN_RxL_1 | 37 | 49 | PF00134 | 0.540 |
DOC_MAPK_gen_1 | 314 | 322 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 325 | 333 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 446 | 455 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 446 | 455 | PF00069 | 0.551 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.498 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.627 |
DOC_USP7_UBL2_3 | 209 | 213 | PF12436 | 0.752 |
DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.705 |
DOC_USP7_UBL2_3 | 321 | 325 | PF12436 | 0.565 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.682 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 435 | 441 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 77 | 84 | PF00244 | 0.471 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.521 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.555 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.415 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.400 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.364 |
LIG_HP1_1 | 451 | 455 | PF01393 | 0.553 |
LIG_Integrin_isoDGR_2 | 138 | 140 | PF01839 | 0.409 |
LIG_LIR_Apic_2 | 3 | 7 | PF02991 | 0.482 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.532 |
LIG_PDZ_Class_2 | 458 | 463 | PF00595 | 0.691 |
LIG_RPA_C_Fungi | 365 | 377 | PF08784 | 0.570 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.482 |
LIG_SH2_SRC | 355 | 358 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.580 |
LIG_SH2_STAT3 | 190 | 193 | PF00017 | 0.591 |
LIG_SH2_STAT3 | 300 | 303 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.463 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.552 |
LIG_SUMO_SIM_par_1 | 451 | 457 | PF11976 | 0.617 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.538 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.428 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.552 |
LIG_TRFH_1 | 4 | 8 | PF08558 | 0.412 |
LIG_UBA3_1 | 319 | 325 | PF00899 | 0.403 |
LIG_ULM_U2AF65_1 | 239 | 244 | PF00076 | 0.698 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.724 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.754 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.550 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.359 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.411 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.749 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.706 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.517 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.511 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.610 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.629 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.545 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.456 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.598 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.515 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.608 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.523 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.653 |
MOD_PK_1 | 251 | 257 | PF00069 | 0.682 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.599 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.616 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.532 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.665 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.481 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.614 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.593 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.681 |
MOD_SUMO_for_1 | 194 | 197 | PF00179 | 0.613 |
MOD_SUMO_for_1 | 245 | 248 | PF00179 | 0.698 |
MOD_SUMO_for_1 | 408 | 411 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 11 | 20 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 136 | 145 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 227 | 233 | PF00179 | 0.724 |
MOD_SUMO_rev_2 | 288 | 295 | PF00179 | 0.587 |
TRG_DiLeu_BaEn_1 | 357 | 362 | PF01217 | 0.479 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILN1 | Leptomonas seymouri | 56% | 100% |
A0A1X0P3Z6 | Trypanosomatidae | 31% | 100% |
A0A3Q8IE88 | Leishmania donovani | 87% | 100% |
A0A3R7MQZ8 | Trypanosoma rangeli | 33% | 100% |
A4HFI7 | Leishmania braziliensis | 71% | 100% |
D0A5R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AD38 | Leishmania major | 86% | 100% |
E9AHD1 | Leishmania infantum | 87% | 100% |
V5BE50 | Trypanosoma cruzi | 28% | 100% |