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: Q4Q8P7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.626 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.561 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.660 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 69 | 79 | PF00244 | 0.661 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.588 |
LIG_Clathr_ClatBox_1 | 165 | 169 | PF01394 | 0.522 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.620 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.571 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.765 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.757 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.704 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.651 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.433 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.671 |
LIG_FXI_DFP_1 | 320 | 324 | PF00024 | 0.575 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 76 | 84 | PF02991 | 0.710 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.708 |
LIG_PDZ_Class_2 | 322 | 327 | PF00595 | 0.629 |
LIG_Pex14_2 | 319 | 323 | PF04695 | 0.638 |
LIG_SH3_1 | 261 | 267 | PF00018 | 0.483 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.679 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.701 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.483 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.493 |
LIG_SUMO_SIM_anti_2 | 269 | 276 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 164 | 170 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 223 | 231 | PF11976 | 0.628 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.713 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.590 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.611 |
MOD_CDK_SPxxK_3 | 14 | 21 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.549 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.643 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.675 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.673 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.522 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.698 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.573 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.724 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.673 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.437 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.670 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.631 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.539 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.668 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.646 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.706 |
MOD_GlcNHglycan | 98 | 102 | PF01048 | 0.683 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.592 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.573 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.601 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.664 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.642 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.668 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.707 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.676 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.565 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.609 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.618 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.664 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.613 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.654 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.663 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.613 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.618 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.663 |
MOD_PKB_1 | 35 | 43 | PF00069 | 0.668 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.604 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.686 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.650 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.714 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.607 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.635 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.503 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.489 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.670 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.704 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.627 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.649 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.678 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.491 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.595 |
TRG_DiLeu_BaEn_1 | 158 | 163 | PF01217 | 0.624 |
TRG_DiLeu_BaEn_3 | 269 | 275 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 161 | 166 | PF01217 | 0.648 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.685 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.613 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHW6 | Leishmania donovani | 88% | 100% |
A4HG64 | Leishmania braziliensis | 52% | 97% |
A4I396 | Leishmania infantum | 88% | 100% |
E9AZI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |