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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3S5H4Y0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.649 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.586 |
CLV_PCSK_PC7_1 | 27 | 33 | PF00082 | 0.625 |
DOC_CKS1_1 | 176 | 181 | PF01111 | 0.550 |
DOC_CYCLIN_RxL_1 | 145 | 155 | PF00134 | 0.392 |
DOC_CYCLIN_RxL_1 | 27 | 39 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 145 | 152 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 214 | 223 | PF00069 | 0.578 |
DOC_MAPK_gen_1 | 241 | 249 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 266 | 275 | PF00069 | 0.580 |
DOC_PP1_RVXF_1 | 146 | 153 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 160 | 166 | PF00149 | 0.544 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.482 |
DOC_PP4_FxxP_1 | 173 | 176 | PF00568 | 0.395 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.556 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 203 | 212 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 214 | 220 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 295 | 304 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 43 | 53 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 57 | 67 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.768 |
LIG_BIR_III_2 | 113 | 117 | PF00653 | 0.545 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.432 |
LIG_EVH1_2 | 116 | 120 | PF00568 | 0.601 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.543 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.662 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.604 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.492 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.618 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.660 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.593 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.609 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.544 |
LIG_LIR_Apic_2 | 172 | 176 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.390 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.373 |
LIG_SH3_1 | 32 | 38 | PF00018 | 0.594 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.538 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.707 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 245 | 252 | PF11976 | 0.598 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.453 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.509 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.590 |
LIG_TRFH_1 | 120 | 124 | PF08558 | 0.605 |
LIG_WW_1 | 2 | 5 | PF00397 | 0.554 |
MOD_CDC14_SPxK_1 | 101 | 104 | PF00782 | 0.732 |
MOD_CDC14_SPxK_1 | 74 | 77 | PF00782 | 0.683 |
MOD_CDK_SPK_2 | 196 | 201 | PF00069 | 0.660 |
MOD_CDK_SPK_2 | 308 | 313 | PF00069 | 0.497 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.683 |
MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.714 |
MOD_CDK_SPxxK_3 | 196 | 203 | PF00069 | 0.590 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.775 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.716 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.692 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.590 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.648 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.611 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.685 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.456 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.444 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.647 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.718 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.495 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.604 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.770 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.778 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.469 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.744 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.678 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.475 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.582 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.723 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.679 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.569 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.722 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.711 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.524 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.511 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.565 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.665 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.721 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.717 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.626 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.492 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.583 |
MOD_PIKK_1 | 284 | 290 | PF00454 | 0.555 |
MOD_PK_1 | 231 | 237 | PF00069 | 0.506 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.537 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.600 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.581 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.766 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.607 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.719 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.775 |
MOD_PKB_1 | 201 | 209 | PF00069 | 0.598 |
MOD_PKB_1 | 241 | 249 | PF00069 | 0.717 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.514 |
MOD_Plk_2-3 | 251 | 257 | PF00069 | 0.661 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.513 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.510 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.721 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.513 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.531 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.664 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.496 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.610 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.683 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.737 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.660 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.646 |
TRG_Pf-PMV_PEXEL_1 | 231 | 236 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 32 | 37 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NLG5 | Trypanosomatidae | 36% | 100% |
A0A3R7LQ19 | Trypanosoma rangeli | 33% | 100% |
A4H3B3 | Leishmania braziliensis | 63% | 100% |
A4HRL1 | Leishmania infantum | 99% | 100% |
C9ZIZ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AC83 | Leishmania major | 88% | 100% |
E9AJH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |