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: E9AF37
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.558 |
CLV_MEL_PAP_1 | 36 | 42 | PF00089 | 0.632 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.546 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.661 |
DOC_CKS1_1 | 249 | 254 | PF01111 | 0.649 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.603 |
DOC_MAPK_gen_1 | 377 | 385 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 79 | 86 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 26 | 32 | PF00149 | 0.550 |
DOC_PP2B_PxIxI_1 | 434 | 440 | PF00149 | 0.492 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.654 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.585 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 126 | 134 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 236 | 245 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 276 | 281 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 379 | 384 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 97 | 103 | PF00244 | 0.629 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.574 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.625 |
LIG_deltaCOP1_diTrp_1 | 335 | 341 | PF00928 | 0.526 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.574 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.583 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.571 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.606 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.631 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.607 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.749 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 335 | 343 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.600 |
LIG_LYPXL_yS_3 | 354 | 357 | PF13949 | 0.520 |
LIG_MYND_1 | 9 | 13 | PF01753 | 0.706 |
LIG_NRBOX | 418 | 424 | PF00104 | 0.536 |
LIG_NRBOX | 51 | 57 | PF00104 | 0.531 |
LIG_PCNA_yPIPBox_3 | 170 | 184 | PF02747 | 0.551 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.521 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.537 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.595 |
LIG_SH2_NCK_1 | 230 | 234 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 387 | 390 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.544 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.675 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.653 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.530 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 171 | 177 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 47 | 54 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 47 | 54 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 80 | 85 | PF11976 | 0.561 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.662 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.558 |
MOD_CDK_SPxxK_3 | 5 | 12 | PF00069 | 0.571 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.552 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.615 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.618 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.524 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.565 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.605 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.597 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.679 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.551 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.725 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.606 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.646 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.698 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.681 |
MOD_CMANNOS | 336 | 339 | PF00535 | 0.521 |
MOD_CMANNOS | 460 | 463 | PF00535 | 0.539 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.593 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.563 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.726 |
MOD_GlcNHglycan | 207 | 211 | PF01048 | 0.585 |
MOD_GlcNHglycan | 296 | 300 | PF01048 | 0.621 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.798 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.638 |
MOD_GlcNHglycan | 398 | 403 | PF01048 | 0.584 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.572 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.623 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.578 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.580 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.620 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.641 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.627 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.671 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.660 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.595 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.598 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.657 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.678 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.576 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.573 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.555 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.501 |
MOD_NEK2_2 | 454 | 459 | PF00069 | 0.572 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.520 |
MOD_PKA_1 | 38 | 44 | PF00069 | 0.628 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.672 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.549 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.559 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.671 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.628 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.633 |
MOD_PKB_1 | 293 | 301 | PF00069 | 0.540 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.515 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.577 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.580 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.551 |
MOD_Plk_2-3 | 168 | 174 | PF00069 | 0.593 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.586 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.678 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.702 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.536 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.532 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.565 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.589 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.521 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.710 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.605 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.677 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.720 |
MOD_SUMO_rev_2 | 20 | 29 | PF00179 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 481 | 486 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.504 |
TRG_NLS_MonoExtC_3 | 36 | 42 | PF00514 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 219 | 223 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSZ3 | Leptomonas seymouri | 47% | 99% |
A0A3Q8IHZ9 | Leishmania donovani | 87% | 100% |
A4HMN5 | Leishmania braziliensis | 69% | 100% |
E9AHV4 | Leishmania infantum | 87% | 100% |
E9B692 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |