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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HI51
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.806 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.814 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.762 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.851 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.852 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.728 |
DOC_CDC14_PxL_1 | 266 | 274 | PF14671 | 0.770 |
DOC_CKS1_1 | 116 | 121 | PF01111 | 0.562 |
DOC_CKS1_1 | 300 | 305 | PF01111 | 0.540 |
DOC_CKS1_1 | 64 | 69 | PF01111 | 0.809 |
DOC_CYCLIN_yClb1_LxF_4 | 399 | 405 | PF00134 | 0.692 |
DOC_CYCLIN_yCln2_LP_2 | 150 | 156 | PF00134 | 0.743 |
DOC_CYCLIN_yCln2_LP_2 | 238 | 241 | PF00134 | 0.589 |
DOC_CYCLIN_yCln2_LP_2 | 300 | 306 | PF00134 | 0.537 |
DOC_MAPK_DCC_7 | 60 | 70 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 296 | 306 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 299 | 308 | PF00069 | 0.559 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.768 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.589 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.673 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.546 |
DOC_PP4_FxxP_1 | 404 | 407 | PF00568 | 0.702 |
DOC_PP4_FxxP_1 | 410 | 413 | PF00568 | 0.628 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.588 |
DOC_USP7_MATH_2 | 156 | 162 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.845 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.803 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.835 |
LIG_14-3-3_CanoR_1 | 197 | 201 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 69 | 78 | PF00244 | 0.701 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.696 |
LIG_CtBP_PxDLS_1 | 130 | 134 | PF00389 | 0.544 |
LIG_EVH1_1 | 113 | 117 | PF00568 | 0.564 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.605 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.588 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.685 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.552 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.573 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.749 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.695 |
LIG_HCF-1_HBM_1 | 420 | 423 | PF13415 | 0.709 |
LIG_LIR_Apic_2 | 61 | 67 | PF02991 | 0.797 |
LIG_LIR_Gen_1 | 254 | 265 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.616 |
LIG_PDZ_Class_1 | 446 | 451 | PF00595 | 0.738 |
LIG_Pex14_2 | 394 | 398 | PF04695 | 0.659 |
LIG_SH2_NCK_1 | 151 | 155 | PF00017 | 0.534 |
LIG_SH2_SRC | 151 | 154 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.566 |
LIG_SH3_1 | 274 | 280 | PF00018 | 0.805 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.697 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.743 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.566 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.819 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.693 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.617 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.825 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.576 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.699 |
LIG_SH3_CIN85_PxpxPR_1 | 110 | 115 | PF14604 | 0.564 |
LIG_SUMO_SIM_par_1 | 412 | 417 | PF11976 | 0.727 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.721 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.715 |
LIG_WRC_WIRS_1 | 391 | 396 | PF05994 | 0.438 |
LIG_WW_3 | 366 | 370 | PF00397 | 0.546 |
MOD_CDK_SPK_2 | 273 | 278 | PF00069 | 0.795 |
MOD_CDK_SPxK_1 | 63 | 69 | PF00069 | 0.805 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.549 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.720 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.604 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.639 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.711 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.739 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.584 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.734 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.723 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.721 |
MOD_DYRK1A_RPxSP_1 | 115 | 119 | PF00069 | 0.561 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.842 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.651 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.771 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.552 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.560 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.776 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.602 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.692 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.525 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.692 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.623 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.669 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.660 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.658 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.554 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.649 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.638 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.642 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.790 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.618 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.687 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.775 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.685 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.746 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.566 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.790 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.580 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.528 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.836 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.717 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.674 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.793 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.727 |
MOD_Plk_2-3 | 432 | 438 | PF00069 | 0.721 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.528 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.588 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.818 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.599 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.697 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.690 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.588 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.615 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.760 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.745 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.542 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.845 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.646 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.733 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.805 |
MOD_SUMO_rev_2 | 437 | 445 | PF00179 | 0.704 |
MOD_SUMO_rev_2 | 50 | 58 | PF00179 | 0.770 |
TRG_DiLeu_BaEn_1 | 54 | 59 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 268 | 273 | PF01217 | 0.774 |
TRG_ER_diArg_1 | 31 | 34 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.670 |
TRG_NLS_MonoExtC_3 | 30 | 35 | PF00514 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IRU8 | Leishmania donovani | 64% | 77% |
A4I5C7 | Leishmania infantum | 64% | 100% |
E9B0M5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4Q7K7 | Leishmania major | 63% | 100% |