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: 34 |
NetGPI | no | yes: 0, no: 34 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
Related structures:
AlphaFold database: E8NHF8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.430 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.664 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.619 |
DOC_ANK_TNKS_1 | 564 | 571 | PF00023 | 0.313 |
DOC_CYCLIN_RxL_1 | 199 | 207 | PF00134 | 0.614 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 288 | 297 | PF00134 | 0.503 |
DOC_CYCLIN_yCln2_LP_2 | 451 | 457 | PF00134 | 0.347 |
DOC_MAPK_DCC_7 | 362 | 371 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 225 | 234 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 362 | 371 | PF00069 | 0.337 |
DOC_PP1_RVXF_1 | 267 | 273 | PF00149 | 0.533 |
DOC_PP1_RVXF_1 | 414 | 420 | PF00149 | 0.269 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.606 |
DOC_PP2B_LxvP_1 | 451 | 454 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.474 |
DOC_PP4_FxxP_1 | 595 | 598 | PF00568 | 0.238 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.313 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.785 |
LIG_14-3-3_CanoR_1 | 407 | 412 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 504 | 511 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 553 | 559 | PF00244 | 0.365 |
LIG_Actin_WH2_2 | 366 | 383 | PF00022 | 0.375 |
LIG_BIR_III_4 | 567 | 571 | PF00653 | 0.423 |
LIG_Clathr_ClatBox_1 | 134 | 138 | PF01394 | 0.633 |
LIG_Clathr_ClatBox_1 | 368 | 372 | PF01394 | 0.353 |
LIG_deltaCOP1_diTrp_1 | 591 | 595 | PF00928 | 0.340 |
LIG_DLG_GKlike_1 | 71 | 78 | PF00625 | 0.612 |
LIG_EH1_1 | 162 | 170 | PF00400 | 0.512 |
LIG_eIF4E_1 | 525 | 531 | PF01652 | 0.300 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.743 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.582 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.542 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.395 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.405 |
LIG_LIR_Apic_2 | 592 | 598 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.565 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.699 |
LIG_PDZ_Class_2 | 604 | 609 | PF00595 | 0.417 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.561 |
LIG_Rb_LxCxE_1 | 397 | 414 | PF01857 | 0.251 |
LIG_SH2_CRK | 525 | 529 | PF00017 | 0.449 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.386 |
LIG_SH2_PTP2 | 177 | 180 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.637 |
LIG_SH2_STAP1 | 484 | 488 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 525 | 529 | PF00017 | 0.330 |
LIG_SH2_STAT3 | 324 | 327 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.410 |
LIG_SH3_2 | 544 | 549 | PF14604 | 0.381 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.641 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.345 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.753 |
LIG_SH3_CIN85_PxpxPR_1 | 64 | 69 | PF14604 | 0.622 |
LIG_SUMO_SIM_anti_2 | 176 | 183 | PF11976 | 0.691 |
LIG_SUMO_SIM_anti_2 | 228 | 234 | PF11976 | 0.544 |
LIG_SUMO_SIM_anti_2 | 436 | 443 | PF11976 | 0.430 |
LIG_SUMO_SIM_anti_2 | 490 | 496 | PF11976 | 0.389 |
LIG_SUMO_SIM_anti_2 | 526 | 532 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.673 |
LIG_SUMO_SIM_par_1 | 436 | 443 | PF11976 | 0.348 |
LIG_TYR_ITIM | 523 | 528 | PF00017 | 0.420 |
LIG_TYR_ITIM | 584 | 589 | PF00017 | 0.356 |
LIG_UBA3_1 | 164 | 170 | PF00899 | 0.533 |
LIG_UBA3_1 | 252 | 260 | PF00899 | 0.471 |
MOD_CAAXbox | 606 | 609 | PF01239 | 0.423 |
MOD_CDC14_SPxK_1 | 546 | 549 | PF00782 | 0.363 |
MOD_CDC14_SPxK_1 | 67 | 70 | PF00782 | 0.712 |
MOD_CDK_SPK_2 | 64 | 69 | PF00069 | 0.711 |
MOD_CDK_SPxK_1 | 543 | 549 | PF00069 | 0.384 |
MOD_CDK_SPxK_1 | 64 | 70 | PF00069 | 0.712 |
MOD_CDK_SPxxK_3 | 64 | 71 | PF00069 | 0.625 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.749 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.624 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.429 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.356 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.577 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.411 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.304 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.533 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.317 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.463 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.421 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.521 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.539 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.481 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.407 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.470 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.472 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.723 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.623 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.649 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.712 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.782 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.452 |
MOD_PKB_1 | 423 | 431 | PF00069 | 0.363 |
MOD_PKB_1 | 69 | 77 | PF00069 | 0.616 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.650 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.633 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.608 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.442 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.319 |
MOD_Plk_2-3 | 262 | 268 | PF00069 | 0.551 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.568 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.624 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.686 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.504 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.373 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.474 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.696 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.373 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.384 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.700 |
TRG_DiLeu_BaEn_1 | 228 | 233 | PF01217 | 0.643 |
TRG_DiLeu_BaEn_1 | 242 | 247 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_1 | 436 | 441 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 413 | 418 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.677 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 422 | 425 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 515 | 518 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.681 |
TRG_NES_CRM1_1 | 251 | 264 | PF08389 | 0.622 |
TRG_NES_CRM1_1 | 378 | 393 | PF08389 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.380 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 57% | 93% |
A0A0N1PB02 | Leptomonas seymouri | 36% | 93% |
A0A0S4J6C6 | Bodo saltans | 32% | 94% |
A0A1X0P9A6 | Trypanosomatidae | 37% | 89% |
A0A3Q8IHH1 | Leishmania donovani | 74% | 83% |
A0A3R7K2Y9 | Trypanosoma rangeli | 36% | 89% |
A0A3S5H668 | Leishmania donovani | 34% | 100% |
A0A3S5H669 | Leishmania donovani | 32% | 96% |
A0A3S7X835 | Leishmania donovani | 36% | 100% |
A4H5C9 | Leishmania braziliensis | 34% | 99% |
A4H5D0 | Leishmania braziliensis | 35% | 100% |
A4HAZ7 | Leishmania braziliensis | 37% | 100% |
A4HAZ9 | Leishmania braziliensis | 39% | 100% |
A4HB01 | Leishmania braziliensis | 40% | 100% |
A4HTM0 | Leishmania infantum | 34% | 100% |
A4HTM1 | Leishmania infantum | 31% | 96% |
A4IA57 | Leishmania infantum | 37% | 100% |
C6K3V8 | Leptomonas seymouri | 34% | 100% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 90% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E8NHF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E8NHR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E8NHS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
Q4Q1U8 | Leishmania major | 75% | 100% |
Q4Q2R4 | Leishmania major | 36% | 100% |
Q4Q310 | Leishmania major | 73% | 100% |
Q4Q312 | Leishmania major | 72% | 100% |
Q4Q340 | Leishmania major | 73% | 100% |
Q4Q342 | Leishmania major | 73% | 100% |
Q4QI90 | Leishmania major | 33% | 100% |
Q4QI91 | Leishmania major | 34% | 98% |