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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HBZ0
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.552 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.514 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.496 |
CLV_PCSK_PC7_1 | 296 | 302 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.526 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.464 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.736 |
DOC_CYCLIN_RxL_1 | 44 | 53 | PF00134 | 0.531 |
DOC_MAPK_gen_1 | 118 | 128 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 7 | 16 | PF00069 | 0.637 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.402 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.635 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 47 | 55 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 9 | 17 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.554 |
LIG_Actin_WH2_2 | 237 | 254 | PF00022 | 0.441 |
LIG_BH_BH3_1 | 47 | 63 | PF00452 | 0.497 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.464 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.486 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.354 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.549 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.450 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.329 |
LIG_LIR_Apic_2 | 127 | 131 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 265 | 272 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.330 |
LIG_RPA_C_Fungi | 231 | 243 | PF08784 | 0.257 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.312 |
LIG_SH2_GRB2like | 307 | 310 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.517 |
LIG_SH3_2 | 201 | 206 | PF14604 | 0.325 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.580 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.562 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.561 |
LIG_SH3_CIN85_PxpxPR_1 | 190 | 195 | PF14604 | 0.455 |
LIG_TYR_ITIM | 305 | 310 | PF00017 | 0.328 |
MOD_CDK_SPK_2 | 150 | 155 | PF00069 | 0.499 |
MOD_CDK_SPK_2 | 190 | 195 | PF00069 | 0.455 |
MOD_CDK_SPxxK_3 | 299 | 306 | PF00069 | 0.374 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.690 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.685 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.515 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.586 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.468 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.501 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.458 |
MOD_Cter_Amidation | 233 | 236 | PF01082 | 0.260 |
MOD_DYRK1A_RPxSP_1 | 215 | 219 | PF00069 | 0.277 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.744 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.708 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.577 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.239 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.661 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.655 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.694 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.677 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.641 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.231 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.455 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.508 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.705 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.481 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.574 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.389 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.414 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.645 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.540 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.505 |
MOD_PK_1 | 301 | 307 | PF00069 | 0.418 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.579 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.430 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.621 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.453 |
MOD_PKB_1 | 290 | 298 | PF00069 | 0.464 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.448 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.467 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.478 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.483 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.404 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.703 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.693 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.667 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.240 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.633 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.501 |
MOD_SUMO_rev_2 | 71 | 81 | PF00179 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 192 | 197 | PF01217 | 0.568 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 108 | 110 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3G8 | Leptomonas seymouri | 62% | 100% |
A0A0S4ILQ9 | Bodo saltans | 37% | 100% |
A0A1X0NI95 | Trypanosomatidae | 39% | 100% |
A0A3Q8IAY8 | Leishmania donovani | 67% | 75% |
A4HZD8 | Leishmania infantum | 67% | 68% |
D0A147 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AVC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 72% |
Q4QC54 | Leishmania major | 71% | 100% |
V5BHB7 | Trypanosoma cruzi | 44% | 100% |