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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B4E0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 451 | 453 | PF00082 | 0.664 |
CLV_PCSK_PC1ET2_1 | 477 | 479 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.460 |
DOC_CYCLIN_RxL_1 | 140 | 152 | PF00134 | 0.433 |
DOC_CYCLIN_RxL_1 | 353 | 364 | PF00134 | 0.415 |
DOC_CYCLIN_yCln2_LP_2 | 380 | 386 | PF00134 | 0.477 |
DOC_MAPK_DCC_7 | 102 | 110 | PF00069 | 0.431 |
DOC_MAPK_DCC_7 | 144 | 153 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 102 | 110 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 142 | 151 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 102 | 110 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 144 | 153 | PF00069 | 0.444 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.427 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.447 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 156 | 166 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 406 | 413 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 452 | 457 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 458 | 463 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 478 | 483 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 6 | 15 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.444 |
LIG_CtBP_PxDLS_1 | 385 | 389 | PF00389 | 0.472 |
LIG_deltaCOP1_diTrp_1 | 301 | 307 | PF00928 | 0.509 |
LIG_EVH1_1 | 332 | 336 | PF00568 | 0.480 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.444 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.694 |
LIG_LIR_Apic_2 | 11 | 17 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 21 | 25 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 299 | 310 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.434 |
LIG_LYPXL_yS_3 | 362 | 365 | PF13949 | 0.446 |
LIG_PCNA_yPIPBox_3 | 116 | 126 | PF02747 | 0.428 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.426 |
LIG_Pex14_2 | 134 | 138 | PF04695 | 0.409 |
LIG_Pex14_2 | 307 | 311 | PF04695 | 0.571 |
LIG_PTB_Apo_2 | 38 | 45 | PF02174 | 0.443 |
LIG_REV1ctd_RIR_1 | 1 | 10 | PF16727 | 0.464 |
LIG_REV1ctd_RIR_1 | 131 | 139 | PF16727 | 0.415 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.424 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.425 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.397 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.481 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.647 |
LIG_SH2_STAT3 | 259 | 262 | PF00017 | 0.619 |
LIG_SH2_STAT3 | 347 | 350 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.464 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.449 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.570 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.499 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.451 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.704 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.681 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.445 |
LIG_TRFH_1 | 195 | 199 | PF08558 | 0.601 |
LIG_TYR_ITIM | 352 | 357 | PF00017 | 0.455 |
LIG_TYR_ITIM | 360 | 365 | PF00017 | 0.389 |
LIG_TYR_ITSM | 119 | 126 | PF00017 | 0.420 |
MOD_CDK_SPK_2 | 401 | 406 | PF00069 | 0.560 |
MOD_CDK_SPK_2 | 424 | 429 | PF00069 | 0.546 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.443 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.636 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.403 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.589 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.669 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.446 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.426 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.490 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.590 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.444 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.558 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.649 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.473 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.430 |
MOD_N-GLC_1 | 266 | 271 | PF02516 | 0.603 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.621 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.435 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.431 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.447 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.426 |
MOD_NEK2_2 | 25 | 30 | PF00069 | 0.446 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.443 |
MOD_NEK2_2 | 97 | 102 | PF00069 | 0.407 |
MOD_OFUCOSY | 76 | 81 | PF10250 | 0.439 |
MOD_OFUCOSY | 95 | 101 | PF10250 | 0.379 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.494 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.697 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.724 |
MOD_PKA_1 | 451 | 457 | PF00069 | 0.646 |
MOD_PKA_1 | 477 | 483 | PF00069 | 0.528 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.546 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.617 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.699 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.517 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.528 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.444 |
MOD_PKB_1 | 142 | 150 | PF00069 | 0.432 |
MOD_PKB_1 | 64 | 72 | PF00069 | 0.460 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.428 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.605 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.418 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.471 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.443 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.527 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.459 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.557 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.606 |
MOD_SUMO_for_1 | 470 | 473 | PF00179 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 462 | 464 | PF00400 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I737 | Leptomonas seymouri | 46% | 100% |
A0A3Q8IHR4 | Leishmania donovani | 78% | 100% |
A4HM09 | Leishmania braziliensis | 62% | 100% |
A4I9E1 | Leishmania infantum | 79% | 100% |
Q4Q3N7 | Leishmania major | 76% | 100% |