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: E9AJF4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.475 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.571 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.517 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.658 |
DOC_MAPK_gen_1 | 122 | 132 | PF00069 | 0.627 |
DOC_PP1_RVXF_1 | 14 | 20 | PF00149 | 0.552 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.527 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.721 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 279 | 288 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 91 | 101 | PF00244 | 0.480 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.598 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.516 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.581 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.661 |
LIG_LIR_Gen_1 | 171 | 181 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 282 | 288 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 8 | 18 | PF02991 | 0.454 |
LIG_LIR_LC3C_4 | 12 | 15 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.449 |
LIG_PDZ_Class_3 | 283 | 288 | PF00595 | 0.660 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.641 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.494 |
LIG_Sin3_3 | 114 | 121 | PF02671 | 0.493 |
LIG_SUMO_SIM_par_1 | 127 | 134 | PF11976 | 0.637 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.586 |
LIG_WRC_WIRS_1 | 170 | 175 | PF05994 | 0.557 |
MOD_CDK_SPK_2 | 137 | 142 | PF00069 | 0.662 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.595 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.605 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.754 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.700 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.809 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.620 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.596 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.584 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.657 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.606 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.697 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.657 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.685 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.760 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.608 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.776 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.635 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.594 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.618 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.607 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.629 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.596 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.707 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.677 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.650 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.705 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.634 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.614 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.587 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.701 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.689 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.480 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.662 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.665 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.661 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.625 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.693 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.642 |
MOD_NEK2_2 | 255 | 260 | PF00069 | 0.522 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.695 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.671 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.618 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.579 |
MOD_PK_1 | 125 | 131 | PF00069 | 0.627 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.675 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.616 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.671 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.504 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.600 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.629 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.692 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.629 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.639 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.679 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.574 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.652 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.635 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I318 | Leptomonas seymouri | 43% | 89% |
A0A3S5H4W5 | Leishmania donovani | 85% | 96% |
A4H385 | Leishmania braziliensis | 65% | 93% |
A4HRJ0 | Leishmania infantum | 84% | 95% |
E9AC58 | Leishmania major | 81% | 100% |