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: E9B4Y9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.672 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.588 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.491 |
CLV_PCSK_FUR_1 | 79 | 83 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.467 |
DEG_APCC_DBOX_1 | 388 | 396 | PF00400 | 0.382 |
DOC_ANK_TNKS_1 | 50 | 57 | PF00023 | 0.730 |
DOC_CKS1_1 | 183 | 188 | PF01111 | 0.730 |
DOC_CKS1_1 | 8 | 13 | PF01111 | 0.654 |
DOC_CYCLIN_RxL_1 | 405 | 416 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 388 | 394 | PF00134 | 0.335 |
DOC_MAPK_gen_1 | 370 | 382 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 375 | 384 | PF00069 | 0.236 |
DOC_PP2B_LxvP_1 | 388 | 391 | PF13499 | 0.335 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.766 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.713 |
DOC_PP4_FxxP_1 | 8 | 11 | PF00568 | 0.651 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.677 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.780 |
LIG_14-3-3_CanoR_1 | 108 | 117 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 143 | 151 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 197 | 202 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 236 | 241 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 279 | 284 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 356 | 362 | PF00244 | 0.780 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.708 |
LIG_Actin_WH2_2 | 118 | 136 | PF00022 | 0.727 |
LIG_Actin_WH2_2 | 381 | 398 | PF00022 | 0.372 |
LIG_BIR_III_2 | 195 | 199 | PF00653 | 0.729 |
LIG_BIR_III_4 | 245 | 249 | PF00653 | 0.603 |
LIG_BRCT_BRCA1_1 | 144 | 148 | PF00533 | 0.631 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.751 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.677 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.585 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.647 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.673 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.744 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.642 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.637 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.786 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.682 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.722 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.776 |
LIG_LIR_Apic_2 | 114 | 119 | PF02991 | 0.714 |
LIG_LIR_Apic_2 | 258 | 264 | PF02991 | 0.716 |
LIG_LIR_Apic_2 | 5 | 11 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 201 | 208 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 290 | 300 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.378 |
LIG_NRBOX | 405 | 411 | PF00104 | 0.431 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.785 |
LIG_SUMO_SIM_anti_2 | 24 | 29 | PF11976 | 0.689 |
LIG_SUMO_SIM_par_1 | 408 | 413 | PF11976 | 0.457 |
LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.620 |
LIG_WW_3 | 10 | 14 | PF00397 | 0.717 |
MOD_CDK_SPK_2 | 74 | 79 | PF00069 | 0.774 |
MOD_CDK_SPK_2 | 98 | 103 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.663 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.768 |
MOD_CDK_SPxxK_3 | 74 | 81 | PF00069 | 0.686 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.715 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.769 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.782 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.704 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.614 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.702 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.676 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.704 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.833 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.694 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.593 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.638 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.382 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.505 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.526 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.590 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.565 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.614 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.492 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.650 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.802 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.747 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.766 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.633 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.776 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.675 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.737 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.645 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.715 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.671 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.582 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.679 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.712 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.723 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.610 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.462 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.518 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.447 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.481 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.559 |
MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.393 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.686 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.745 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.736 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.728 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.347 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.358 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.658 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.621 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.725 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.468 |
MOD_PK_1 | 236 | 242 | PF00069 | 0.757 |
MOD_PK_1 | 279 | 285 | PF00069 | 0.658 |
MOD_PK_1 | 375 | 381 | PF00069 | 0.294 |
MOD_PKA_1 | 371 | 377 | PF00069 | 0.624 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.669 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.783 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.786 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.782 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.771 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.630 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.624 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.719 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.721 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.602 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.648 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.760 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.596 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.735 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.738 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.389 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.721 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.660 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.707 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.758 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.637 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.767 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.676 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.679 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.740 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.781 |
MOD_SUMO_rev_2 | 256 | 262 | PF00179 | 0.698 |
TRG_DiLeu_BaEn_1 | 405 | 410 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 372 | 377 | PF01217 | 0.577 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.725 |
TRG_NES_CRM1_1 | 24 | 37 | PF08389 | 0.680 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8U0 | Leptomonas seymouri | 30% | 95% |
A0A3Q8IHI2 | Leishmania donovani | 84% | 100% |
A4HBI6 | Leishmania braziliensis | 56% | 100% |
A4I9Y1 | Leishmania infantum | 84% | 100% |
Q4Q2Z7 | Leishmania major | 80% | 100% |