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: E9AYI8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.624 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.597 |
DOC_CYCLIN_yCln2_LP_2 | 284 | 290 | PF00134 | 0.442 |
DOC_MAPK_MEF2A_6 | 181 | 189 | PF00069 | 0.661 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.610 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.392 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.583 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.547 |
LIG_14-3-3_CanoR_1 | 200 | 208 | PF00244 | 0.616 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.625 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.633 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.504 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.448 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.622 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.556 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.697 |
LIG_LIR_Apic_2 | 154 | 159 | PF02991 | 0.641 |
LIG_LIR_LC3C_4 | 229 | 233 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.528 |
LIG_Pex14_2 | 297 | 301 | PF04695 | 0.401 |
LIG_SH2_PTP2 | 56 | 59 | PF00017 | 0.556 |
LIG_SH2_SRC | 56 | 59 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.591 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.488 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.659 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.484 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.551 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.579 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.602 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.500 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.534 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.657 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.498 |
MOD_CDK_SPK_2 | 207 | 212 | PF00069 | 0.676 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.494 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.726 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.668 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.651 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.762 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.684 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.648 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.634 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.709 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.627 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.598 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.640 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.567 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.660 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.687 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.733 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.642 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.716 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.621 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.720 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.561 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.581 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.587 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.742 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.594 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.570 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.585 |
MOD_LATS_1 | 161 | 167 | PF00433 | 0.640 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.509 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.440 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.638 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.461 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.587 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.589 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.606 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.592 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.627 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.808 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.441 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.462 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.708 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.699 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.594 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.704 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.645 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.563 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.441 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.564 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.546 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.674 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBU5 | Leptomonas seymouri | 46% | 97% |
A0A3S7X039 | Leishmania donovani | 87% | 100% |
A4HF52 | Leishmania braziliensis | 66% | 100% |
A4I2D6 | Leishmania infantum | 87% | 100% |
Q4Q8Y4 | Leishmania major | 84% | 100% |