Kinetoplastid-unique proteins with many disordered segments and a hydrophobic C-terminal region.
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9ADV3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.475 |
CLV_PCSK_PC7_1 | 484 | 490 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.484 |
DEG_APCC_DBOX_1 | 130 | 138 | PF00400 | 0.687 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.707 |
DOC_CDC14_PxL_1 | 445 | 453 | PF14671 | 0.425 |
DOC_CKS1_1 | 10 | 15 | PF01111 | 0.702 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.545 |
DOC_CYCLIN_RxL_1 | 368 | 377 | PF00134 | 0.644 |
DOC_CYCLIN_yCln2_LP_2 | 451 | 457 | PF00134 | 0.259 |
DOC_MAPK_gen_1 | 48 | 55 | PF00069 | 0.645 |
DOC_PP1_SILK_1 | 297 | 302 | PF00149 | 0.525 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.616 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.695 |
DOC_PP4_FxxP_1 | 468 | 471 | PF00568 | 0.341 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 206 | 210 | PF12436 | 0.675 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.673 |
LIG_14-3-3_CanoR_1 | 385 | 393 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 396 | 404 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 84 | 89 | PF00244 | 0.682 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.588 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.730 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.589 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.526 |
LIG_BRCT_BRCA1_2 | 32 | 38 | PF00533 | 0.613 |
LIG_deltaCOP1_diTrp_1 | 410 | 415 | PF00928 | 0.300 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.741 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.599 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.682 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.491 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.340 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.717 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.691 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.579 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.647 |
LIG_FXI_DFP_1 | 388 | 392 | PF00024 | 0.384 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.725 |
LIG_LIR_Gen_1 | 225 | 235 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 354 | 361 | PF02991 | 0.741 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 409 | 419 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.384 |
LIG_Pex14_1 | 411 | 415 | PF04695 | 0.300 |
LIG_SH2_CRK | 107 | 111 | PF00017 | 0.734 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.620 |
LIG_SH2_CRK | 288 | 292 | PF00017 | 0.597 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.593 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.625 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 107 | 111 | PF00017 | 0.659 |
LIG_SH2_NCK_1 | 288 | 292 | PF00017 | 0.622 |
LIG_SH2_PTP2 | 21 | 24 | PF00017 | 0.578 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.578 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 425 | 428 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.422 |
LIG_SH3_1 | 107 | 113 | PF00018 | 0.642 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.659 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.768 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.631 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.625 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.715 |
LIG_SH3_4 | 206 | 213 | PF00018 | 0.659 |
LIG_SUMO_SIM_anti_2 | 289 | 295 | PF11976 | 0.568 |
LIG_SUMO_SIM_anti_2 | 460 | 465 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 470 | 476 | PF11976 | 0.344 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.665 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.594 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.601 |
LIG_TYR_ITIM | 369 | 374 | PF00017 | 0.621 |
LIG_TYR_ITIM | 414 | 419 | PF00017 | 0.300 |
LIG_WW_3 | 14 | 18 | PF00397 | 0.620 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.759 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.620 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.729 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.699 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.619 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.476 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.711 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.667 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.691 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.566 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.720 |
MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.460 |
MOD_GlcNHglycan | 101 | 105 | PF01048 | 0.503 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.527 |
MOD_GlcNHglycan | 119 | 123 | PF01048 | 0.444 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.514 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.533 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.420 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.508 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.674 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.604 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.671 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.613 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.335 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.707 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.718 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.626 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.385 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.694 |
MOD_PK_1 | 61 | 67 | PF00069 | 0.654 |
MOD_PK_1 | 84 | 90 | PF00069 | 0.700 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.707 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.592 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.643 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.671 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.626 |
MOD_PKB_1 | 82 | 90 | PF00069 | 0.643 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.657 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.677 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.728 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.578 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.656 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.621 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.515 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.732 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.671 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.786 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.542 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.664 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.669 |
MOD_SUMO_rev_2 | 213 | 219 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 319 | 326 | PF00179 | 0.648 |
MOD_SUMO_rev_2 | 354 | 363 | PF00179 | 0.659 |
TRG_DiLeu_BaEn_1 | 365 | 370 | PF01217 | 0.662 |
TRG_DiLeu_BaEn_2 | 31 | 37 | PF01217 | 0.620 |
TRG_DiLeu_BaLyEn_6 | 468 | 473 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 372 | 377 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF35 | Leptomonas seymouri | 68% | 87% |
A0A0S4JJG2 | Bodo saltans | 34% | 100% |
A0A3Q8IF28 | Leishmania donovani | 94% | 86% |
A4HHA7 | Leishmania braziliensis | 82% | 100% |
A4I4F3 | Leishmania infantum | 94% | 86% |
C9ZLK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 99% |
E9ALX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 86% |
V5BH52 | Trypanosoma cruzi | 40% | 96% |