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: E9AMC8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.682 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.579 |
DEG_SCF_FBW7_1 | 208 | 214 | PF00400 | 0.541 |
DEG_SCF_FBW7_1 | 22 | 29 | PF00400 | 0.604 |
DEG_SCF_TRCP1_1 | 167 | 172 | PF00400 | 0.575 |
DOC_CKS1_1 | 208 | 213 | PF01111 | 0.539 |
DOC_CYCLIN_RxL_1 | 277 | 286 | PF00134 | 0.615 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.633 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.660 |
DOC_PP4_FxxP_1 | 138 | 141 | PF00568 | 0.588 |
DOC_PP4_MxPP_1 | 17 | 20 | PF00568 | 0.650 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.669 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 83 | 91 | PF00244 | 0.609 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.655 |
LIG_EVH1_2 | 30 | 34 | PF00568 | 0.573 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.710 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.664 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.636 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.567 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.611 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.640 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.649 |
LIG_Integrin_isoDGR_2 | 364 | 366 | PF01839 | 0.521 |
LIG_Integrin_RGD_1 | 269 | 271 | PF01839 | 0.524 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 337 | 348 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.649 |
LIG_MYND_3 | 205 | 209 | PF01753 | 0.522 |
LIG_NRBOX | 98 | 104 | PF00104 | 0.556 |
LIG_PDZ_Class_2 | 393 | 398 | PF00595 | 0.620 |
LIG_Pex14_1 | 336 | 340 | PF04695 | 0.655 |
LIG_RPA_C_Fungi | 104 | 116 | PF08784 | 0.496 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.646 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.737 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.663 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.654 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.528 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 392 | 397 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.626 |
LIG_ULM_U2AF65_1 | 218 | 224 | PF00076 | 0.640 |
LIG_WRC_WIRS_1 | 91 | 96 | PF05994 | 0.571 |
MOD_CDC14_SPxK_1 | 80 | 83 | PF00782 | 0.573 |
MOD_CDK_SPxK_1 | 77 | 83 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 300 | 307 | PF00069 | 0.645 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.659 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.575 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.659 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.616 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.683 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.649 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.679 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.766 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.699 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.656 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.606 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.611 |
MOD_CMANNOS | 223 | 226 | PF00535 | 0.683 |
MOD_Cter_Amidation | 364 | 367 | PF01082 | 0.523 |
MOD_DYRK1A_RPxSP_1 | 92 | 96 | PF00069 | 0.451 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.716 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.656 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.676 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.655 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.600 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.603 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.578 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.649 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.602 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.622 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.569 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.656 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.672 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.603 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.644 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.593 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.571 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.678 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.606 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.574 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.754 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.552 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.596 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.666 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.672 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.657 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.726 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.450 |
MOD_PKA_1 | 218 | 224 | PF00069 | 0.640 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.762 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.645 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.617 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.500 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.567 |
MOD_PKB_1 | 220 | 228 | PF00069 | 0.528 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.666 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.529 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.639 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.747 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.695 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.770 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.620 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.626 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.671 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.644 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.499 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.550 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.661 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.488 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.646 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.502 |
TRG_NES_CRM1_1 | 194 | 209 | PF08389 | 0.617 |
TRG_NLS_MonoExtC_3 | 217 | 222 | PF00514 | 0.640 |
TRG_NLS_MonoExtN_4 | 217 | 223 | PF00514 | 0.681 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H653 | Leishmania donovani | 76% | 100% |
A4H5B6 | Leishmania braziliensis | 54% | 100% |
A4HTJ7 | Leishmania infantum | 76% | 96% |
Q4QIC0 | Leishmania major | 79% | 100% |