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: 35 |
NetGPI | no | yes: 0, no: 35 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: Q4Q1U8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.669 |
CLV_Separin_Metazoa | 53 | 57 | PF03568 | 0.694 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.546 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.444 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.270 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.626 |
DOC_CYCLIN_RxL_1 | 139 | 147 | PF00134 | 0.629 |
DOC_CYCLIN_yCln2_LP_2 | 434 | 440 | PF00134 | 0.333 |
DOC_CYCLIN_yCln2_LP_2 | 568 | 574 | PF00134 | 0.363 |
DOC_MAPK_DCC_7 | 395 | 405 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 177 | 186 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 341 | 351 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 123 | 130 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.557 |
DOC_PP2B_LxvP_1 | 434 | 437 | PF13499 | 0.403 |
DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.487 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.475 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.787 |
LIG_14-3-3_CanoR_1 | 312 | 320 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 390 | 395 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 487 | 494 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 536 | 542 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.633 |
LIG_Actin_WH2_2 | 349 | 366 | PF00022 | 0.380 |
LIG_BIR_III_4 | 550 | 554 | PF00653 | 0.428 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.449 |
LIG_Clathr_ClatBox_1 | 351 | 355 | PF01394 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 575 | 578 | PF00928 | 0.347 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.603 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.525 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.429 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.754 |
LIG_Integrin_RGD_1 | 68 | 70 | PF01839 | 0.507 |
LIG_LIR_Apic_2 | 452 | 457 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 116 | 121 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 507 | 516 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 116 | 120 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 507 | 511 | PF02991 | 0.431 |
LIG_PDZ_Class_2 | 587 | 592 | PF00595 | 0.426 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.576 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.404 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.461 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 569 | 573 | PF00017 | 0.409 |
LIG_SH2_PTP2 | 117 | 120 | PF00017 | 0.566 |
LIG_SH2_SRC | 467 | 470 | PF00017 | 0.504 |
LIG_SH2_SRC | 569 | 572 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.370 |
LIG_SH3_2 | 527 | 532 | PF14604 | 0.392 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.649 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.424 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.700 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.395 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.697 |
LIG_SUMO_SIM_anti_2 | 168 | 174 | PF11976 | 0.554 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 347 | 353 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 419 | 426 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 473 | 479 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 419 | 426 | PF11976 | 0.432 |
LIG_TYR_ITIM | 506 | 511 | PF00017 | 0.540 |
LIG_TYR_ITIM | 567 | 572 | PF00017 | 0.468 |
LIG_UBA3_1 | 118 | 123 | PF00899 | 0.582 |
MOD_CAAXbox | 589 | 592 | PF01239 | 0.533 |
MOD_CDC14_SPxK_1 | 529 | 532 | PF00782 | 0.452 |
MOD_CDC14_SPxK_1 | 7 | 10 | PF00782 | 0.636 |
MOD_CDK_SPK_2 | 4 | 9 | PF00069 | 0.647 |
MOD_CDK_SPxK_1 | 4 | 10 | PF00069 | 0.645 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.482 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.615 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.538 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.494 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.685 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.480 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.679 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.533 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.577 |
MOD_Cter_Amidation | 57 | 60 | PF01082 | 0.643 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.579 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.498 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.613 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.651 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.666 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.530 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.587 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.639 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.490 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.532 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.599 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.633 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.522 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.402 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.516 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.649 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.564 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.647 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.712 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.598 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.612 |
MOD_PKB_1 | 406 | 414 | PF00069 | 0.444 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.541 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.520 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.543 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.522 |
MOD_Plk_2-3 | 202 | 208 | PF00069 | 0.437 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.552 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.627 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.411 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.602 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.597 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.650 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.460 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.482 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_1 | 182 | 187 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_1 | 188 | 193 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_1 | 419 | 424 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 517 | 519 | PF00400 | 0.579 |
TRG_NES_CRM1_1 | 191 | 204 | PF08389 | 0.538 |
TRG_NES_CRM1_1 | 361 | 376 | PF08389 | 0.439 |
TRG_NLS_MonoExtN_4 | 140 | 145 | PF00514 | 0.659 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 63% | 90% |
A0A0N1PB02 | Leptomonas seymouri | 40% | 90% |
A0A0S4J6C6 | Bodo saltans | 33% | 91% |
A0A1X0P9A6 | Trypanosomatidae | 36% | 87% |
A0A3Q8IHH1 | Leishmania donovani | 87% | 81% |
A0A3R7K2Y9 | Trypanosoma rangeli | 39% | 86% |
A0A3S5H668 | Leishmania donovani | 39% | 100% |
A0A3S5H669 | Leishmania donovani | 38% | 93% |
A0A3S7X835 | Leishmania donovani | 39% | 100% |
A4H5C9 | Leishmania braziliensis | 38% | 100% |
A4H5D0 | Leishmania braziliensis | 40% | 99% |
A4HAZ7 | Leishmania braziliensis | 41% | 100% |
A4HAZ9 | Leishmania braziliensis | 42% | 95% |
A4HB01 | Leishmania braziliensis | 42% | 100% |
A4HTM0 | Leishmania infantum | 38% | 100% |
A4HTM1 | Leishmania infantum | 38% | 93% |
A4IA57 | Leishmania infantum | 39% | 100% |
C6K3V8 | Leptomonas seymouri | 38% | 98% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 88% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 94% |
E8NHF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 97% |
E8NHR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E8NHS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 93% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
Q4Q2R4 | Leishmania major | 40% | 100% |
Q4Q310 | Leishmania major | 99% | 89% |
Q4Q312 | Leishmania major | 99% | 89% |
Q4Q340 | Leishmania major | 99% | 89% |
Q4Q342 | Leishmania major | 100% | 89% |
Q4QI90 | Leishmania major | 38% | 93% |
Q4QI91 | Leishmania major | 38% | 100% |