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: E9AIJ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.545 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.400 |
CLV_PCSK_PC7_1 | 234 | 240 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.437 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.420 |
DEG_SPOP_SBC_1 | 153 | 157 | PF00917 | 0.515 |
DOC_CYCLIN_RxL_1 | 234 | 244 | PF00134 | 0.540 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 119 | 127 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 298 | 308 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 63 | 71 | PF00244 | 0.544 |
LIG_APCC_ABBA_1 | 258 | 263 | PF00400 | 0.529 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.534 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.553 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.544 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.520 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.402 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.691 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.660 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.379 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.425 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.411 |
LIG_NRBOX | 254 | 260 | PF00104 | 0.400 |
LIG_Pex14_1 | 35 | 39 | PF04695 | 0.559 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.378 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.652 |
LIG_SUMO_SIM_anti_2 | 267 | 273 | PF11976 | 0.576 |
MOD_CDK_SPxK_1 | 187 | 193 | PF00069 | 0.584 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.668 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.572 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.608 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.712 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.659 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.617 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.705 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.666 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.501 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.521 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.612 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.708 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.733 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.561 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.626 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.665 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.495 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.632 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.720 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.675 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.541 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.664 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.440 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.600 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.596 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.445 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.556 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.499 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.443 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.392 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.392 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.549 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.609 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.362 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.580 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.628 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.629 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.633 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.517 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.693 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.610 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.645 |
MOD_SUMO_rev_2 | 110 | 120 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 52 | 61 | PF00179 | 0.571 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 111 | 116 | PF00026 | 0.572 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WW39 | Leishmania donovani | 62% | 70% |
A4HYY2 | Leishmania infantum | 62% | 70% |
E9AUS8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 70% |
Q4QCQ5 | Leishmania major | 62% | 100% |