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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AZ00
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.613 |
DEG_COP1_1 | 263 | 272 | PF00400 | 0.581 |
DEG_MDM2_SWIB_1 | 159 | 166 | PF02201 | 0.532 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.656 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.681 |
DEG_SPOP_SBC_1 | 221 | 225 | PF00917 | 0.548 |
DOC_AGCK_PIF_2 | 68 | 73 | PF00069 | 0.630 |
DOC_CYCLIN_RxL_1 | 143 | 153 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 35 | 45 | PF00069 | 0.603 |
DOC_MAPK_MEF2A_6 | 39 | 47 | PF00069 | 0.600 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.622 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.460 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.769 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.757 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.577 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.524 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.589 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.666 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.586 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.594 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.649 |
LIG_GBD_Chelix_1 | 235 | 243 | PF00786 | 0.693 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 263 | 272 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.697 |
LIG_NRP_CendR_1 | 278 | 280 | PF00754 | 0.626 |
LIG_Pex14_2 | 159 | 163 | PF04695 | 0.489 |
LIG_REV1ctd_RIR_1 | 71 | 79 | PF16727 | 0.538 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.601 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.429 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.555 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.512 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.579 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 271 | 277 | PF11976 | 0.611 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.675 |
MOD_CDK_SPK_2 | 141 | 146 | PF00069 | 0.370 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.715 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.740 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.597 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.695 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.734 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.592 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.663 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.672 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.547 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.590 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.706 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.677 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.631 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.639 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.684 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.773 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.717 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.488 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.727 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.645 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.549 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.623 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.701 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.777 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.737 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.510 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.774 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.635 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.368 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.719 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.584 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.619 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.592 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.586 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.368 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.579 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.606 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.542 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.489 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.541 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.698 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.697 |
TRG_DiLeu_BaEn_2 | 130 | 136 | PF01217 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.619 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6J0 | Leptomonas seymouri | 46% | 100% |
A0A1X0P427 | Trypanosomatidae | 32% | 100% |
A0A3S7X0L8 | Leishmania donovani | 87% | 100% |
A0A422N2W4 | Trypanosoma rangeli | 30% | 100% |
A4HFM2 | Leishmania braziliensis | 74% | 100% |
A4I2Q0 | Leishmania infantum | 88% | 100% |
D0A5V2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AD76 | Leishmania major | 87% | 100% |