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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9ALX7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.589 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.481 |
CLV_PCSK_PC7_1 | 564 | 570 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.776 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.676 |
DEG_APCC_DBOX_1 | 210 | 218 | PF00400 | 0.569 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.479 |
DEG_SPOP_SBC_1 | 163 | 167 | PF00917 | 0.511 |
DOC_CDC14_PxL_1 | 525 | 533 | PF14671 | 0.427 |
DOC_CKS1_1 | 303 | 308 | PF01111 | 0.376 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.511 |
DOC_CYCLIN_RxL_1 | 448 | 457 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 531 | 537 | PF00134 | 0.271 |
DOC_MAPK_gen_1 | 128 | 135 | PF00069 | 0.485 |
DOC_MAPK_RevD_3 | 414 | 430 | PF00069 | 0.420 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.471 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.524 |
DOC_PP4_FxxP_1 | 548 | 551 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.518 |
DOC_USP7_UBL2_3 | 286 | 290 | PF12436 | 0.489 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.486 |
LIG_14-3-3_CanoR_1 | 128 | 136 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 16 | 21 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 162 | 169 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 35 | 39 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 465 | 473 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 48 | 55 | PF00244 | 0.367 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_2 | 112 | 118 | PF00533 | 0.471 |
LIG_deltaCOP1_diTrp_1 | 490 | 495 | PF00928 | 0.403 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.534 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.469 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.507 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.454 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.474 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.438 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.354 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.431 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.534 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.508 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.410 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.479 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.466 |
LIG_FXI_DFP_1 | 468 | 472 | PF00024 | 0.628 |
LIG_Integrin_isoDGR_2 | 26 | 28 | PF01839 | 0.696 |
LIG_LIR_Apic_2 | 113 | 119 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 434 | 441 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 478 | 488 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 489 | 499 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 515 | 520 | PF02991 | 0.410 |
LIG_Pex14_1 | 491 | 495 | PF04695 | 0.402 |
LIG_SH2_CRK | 187 | 191 | PF00017 | 0.538 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.444 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.442 |
LIG_SH2_CRK | 385 | 389 | PF00017 | 0.473 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.473 |
LIG_SH2_CRK | 496 | 500 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 368 | 372 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 101 | 104 | PF00017 | 0.405 |
LIG_SH2_SRC | 101 | 104 | PF00017 | 0.405 |
LIG_SH2_SRC | 368 | 371 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 488 | 492 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 169 | 172 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 505 | 508 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.463 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.442 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.402 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.633 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.500 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.512 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.443 |
LIG_SH3_4 | 286 | 293 | PF00018 | 0.485 |
LIG_SUMO_SIM_anti_2 | 17 | 22 | PF11976 | 0.474 |
LIG_SUMO_SIM_anti_2 | 369 | 375 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 540 | 545 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 550 | 556 | PF11976 | 0.359 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.429 |
LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.474 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.413 |
LIG_TYR_ITIM | 449 | 454 | PF00017 | 0.473 |
LIG_TYR_ITIM | 494 | 499 | PF00017 | 0.389 |
LIG_WW_3 | 94 | 98 | PF00397 | 0.459 |
MOD_CDK_SPK_2 | 73 | 78 | PF00069 | 0.503 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.431 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.582 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.455 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.504 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.409 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.584 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.493 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.509 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.494 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.501 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.395 |
MOD_Cter_Amidation | 427 | 430 | PF01082 | 0.672 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.731 |
MOD_GlcNHglycan | 181 | 185 | PF01048 | 0.727 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.748 |
MOD_GlcNHglycan | 199 | 203 | PF01048 | 0.680 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.772 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.694 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.656 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.487 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.476 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.528 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.445 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.552 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.522 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.446 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.498 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.350 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.607 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.597 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.675 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.532 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.543 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.474 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.501 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.399 |
MOD_PK_1 | 141 | 147 | PF00069 | 0.509 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.407 |
MOD_PK_1 | 164 | 170 | PF00069 | 0.505 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.487 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.487 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.486 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.569 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.468 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.425 |
MOD_PKB_1 | 162 | 170 | PF00069 | 0.490 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.406 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.461 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.530 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.543 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.444 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.393 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.407 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.522 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.569 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.493 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.466 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.476 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.543 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.537 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.372 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.531 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.484 |
MOD_SUMO_rev_2 | 434 | 443 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 445 | 450 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_2 | 111 | 117 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 548 | 553 | PF01217 | 0.343 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 341 | 346 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 452 | 457 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF35 | Leptomonas seymouri | 69% | 100% |
A0A0S4JJG2 | Bodo saltans | 33% | 100% |
A0A3Q8IF28 | Leishmania donovani | 90% | 100% |
A4HHA7 | Leishmania braziliensis | 84% | 100% |
A4I4F3 | Leishmania infantum | 90% | 100% |
C9ZLK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ADV3 | Leishmania major | 92% | 100% |