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:0030008 | TRAPP complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0099023 | vesicle tethering complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1990072 | TRAPPIII protein complex | 4 | 1 |
Related structures:
AlphaFold database: A0A3S5H5C3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.356 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.294 |
CLV_C14_Caspase3-7 | 557 | 561 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.689 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.617 |
CLV_PCSK_FUR_1 | 83 | 87 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 446 | 448 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.545 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.656 |
DEG_ODPH_VHL_1 | 512 | 525 | PF01847 | 0.456 |
DEG_SPOP_SBC_1 | 448 | 452 | PF00917 | 0.556 |
DOC_CYCLIN_RxL_1 | 173 | 182 | PF00134 | 0.411 |
DOC_CYCLIN_RxL_1 | 418 | 428 | PF00134 | 0.456 |
DOC_CYCLIN_RxL_1 | 521 | 531 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 39 | 45 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 106 | 115 | PF00069 | 0.502 |
DOC_MAPK_HePTP_8 | 285 | 297 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 108 | 117 | PF00069 | 0.662 |
DOC_MAPK_MEF2A_6 | 288 | 297 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 346 | 354 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 500 | 509 | PF00069 | 0.403 |
DOC_PP1_RVXF_1 | 220 | 227 | PF00149 | 0.302 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.302 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.354 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.427 |
DOC_PP2B_LxvP_1 | 39 | 42 | PF13499 | 0.572 |
DOC_PP2B_LxvP_1 | 568 | 571 | PF13499 | 0.482 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.667 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.785 |
LIG_14-3-3_CanoR_1 | 180 | 184 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 248 | 258 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 392 | 397 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 447 | 456 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 562 | 570 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 9 | 16 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.766 |
LIG_Actin_WH2_2 | 160 | 177 | PF00022 | 0.356 |
LIG_Actin_WH2_2 | 232 | 247 | PF00022 | 0.420 |
LIG_Actin_WH2_2 | 358 | 375 | PF00022 | 0.411 |
LIG_Actin_WH2_2 | 416 | 434 | PF00022 | 0.402 |
LIG_AP2alpha_2 | 79 | 81 | PF02296 | 0.640 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.405 |
LIG_BRCT_BRCA1_1 | 533 | 537 | PF00533 | 0.501 |
LIG_CSL_BTD_1 | 568 | 571 | PF09270 | 0.482 |
LIG_EH1_1 | 362 | 370 | PF00400 | 0.420 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.678 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.365 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.612 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.425 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.430 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.559 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.561 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.454 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.377 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.522 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.418 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.436 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.697 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.475 |
LIG_LIR_Apic_2 | 213 | 217 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 190 | 200 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 465 | 476 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 79 | 89 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 465 | 471 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 487 | 493 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.522 |
LIG_NRBOX | 524 | 530 | PF00104 | 0.444 |
LIG_PCNA_yPIPBox_3 | 414 | 424 | PF02747 | 0.378 |
LIG_PDZ_Class_2 | 631 | 636 | PF00595 | 0.447 |
LIG_Pex14_1 | 226 | 230 | PF04695 | 0.427 |
LIG_PTAP_UEV_1 | 169 | 174 | PF05743 | 0.245 |
LIG_SH2_CRK | 192 | 196 | PF00017 | 0.420 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.534 |
LIG_SH2_CRK | 518 | 522 | PF00017 | 0.404 |
LIG_SH2_NCK_1 | 192 | 196 | PF00017 | 0.420 |
LIG_SH2_PTP2 | 246 | 249 | PF00017 | 0.420 |
LIG_SH2_SRC | 215 | 218 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 192 | 196 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.323 |
LIG_SH3_1 | 473 | 479 | PF00018 | 0.525 |
LIG_SH3_2 | 170 | 175 | PF14604 | 0.411 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.706 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.445 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.410 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.729 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.429 |
LIG_SUMO_SIM_anti_2 | 538 | 543 | PF11976 | 0.403 |
LIG_SUMO_SIM_anti_2 | 554 | 560 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 572 | 579 | PF11976 | 0.558 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.245 |
MOD_CDK_SPK_2 | 387 | 392 | PF00069 | 0.423 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.803 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.427 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.447 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.359 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.391 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.790 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.529 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.624 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.445 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.669 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.766 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.398 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.457 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.696 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.607 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.752 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.318 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.438 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.382 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.390 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.557 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.339 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.652 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.473 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.645 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.574 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.625 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.453 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.336 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.385 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.576 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.495 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.401 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.802 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.494 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.448 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.699 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.696 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.410 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.429 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.345 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.539 |
MOD_N-GLC_2 | 116 | 118 | PF02516 | 0.573 |
MOD_N-GLC_2 | 333 | 335 | PF02516 | 0.245 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.687 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.335 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.431 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.345 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.376 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.466 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.506 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.476 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.418 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.655 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.739 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.767 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.427 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.467 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.591 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.512 |
MOD_PK_1 | 590 | 596 | PF00069 | 0.605 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.427 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.402 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.601 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.482 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.649 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.741 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.420 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.473 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.345 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.324 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.633 |
MOD_Plk_2-3 | 626 | 632 | PF00069 | 0.468 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.420 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.479 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.476 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.399 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.493 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.391 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.705 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.592 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.784 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 476 | 481 | PF01217 | 0.634 |
TRG_DiLeu_BaLyEn_6 | 521 | 526 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.537 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 435 | 439 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHB8 | Leptomonas seymouri | 49% | 98% |
A0A1X0NLJ7 | Trypanosomatidae | 30% | 100% |
A0A3R7LPQ4 | Trypanosoma rangeli | 29% | 100% |
A4H407 | Leishmania braziliensis | 72% | 100% |
A4HS69 | Leishmania infantum | 99% | 100% |
C9ZY64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AK56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
O97215 | Leishmania major | 90% | 100% |
V5BIB6 | Trypanosoma cruzi | 29% | 100% |