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: E9ATZ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.409 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.772 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.709 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.467 |
DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.667 |
DEG_SPOP_SBC_1 | 188 | 192 | PF00917 | 0.755 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.541 |
DOC_CYCLIN_RxL_1 | 43 | 53 | PF00134 | 0.560 |
DOC_MAPK_gen_1 | 43 | 52 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 214 | 222 | PF00069 | 0.508 |
DOC_MIT_MIM_1 | 7 | 17 | PF04212 | 0.461 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.434 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.675 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.755 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 338 | 343 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.406 |
LIG_Actin_WH2_2 | 191 | 206 | PF00022 | 0.685 |
LIG_APCC_ABBA_1 | 331 | 336 | PF00400 | 0.640 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.537 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.621 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.467 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.516 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.430 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.473 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.711 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.551 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.700 |
LIG_LIR_Gen_1 | 157 | 162 | PF02991 | 0.713 |
LIG_LIR_Gen_1 | 172 | 179 | PF02991 | 0.727 |
LIG_LIR_Gen_1 | 276 | 286 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 325 | 334 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.630 |
LIG_MYND_1 | 201 | 205 | PF01753 | 0.683 |
LIG_Pex14_2 | 261 | 265 | PF04695 | 0.531 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.659 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.712 |
LIG_SH2_GRB2like | 279 | 282 | PF00017 | 0.572 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.502 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.547 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.712 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.570 |
LIG_SH2_STAT3 | 307 | 310 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.397 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.666 |
LIG_SUMO_SIM_anti_2 | 174 | 180 | PF11976 | 0.757 |
LIG_SUMO_SIM_anti_2 | 6 | 12 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 99 | 104 | PF11976 | 0.534 |
LIG_TRAF2_1 | 352 | 355 | PF00917 | 0.637 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.705 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.629 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.532 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.767 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.692 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.514 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.584 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.587 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.755 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.542 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.509 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.558 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.691 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.689 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.550 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.603 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.442 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.639 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.601 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.638 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.492 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.332 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.669 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.548 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.414 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.475 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.698 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.587 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.744 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.480 |
MOD_PKA_1 | 312 | 318 | PF00069 | 0.596 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.404 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.743 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.675 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.463 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.572 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.571 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.639 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.543 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.533 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.496 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.658 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.754 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.715 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.437 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.629 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.523 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.534 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.533 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.710 |
MOD_SUMO_for_1 | 352 | 355 | PF00179 | 0.655 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.712 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.572 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 48 | 53 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P9D5 | Leptomonas seymouri | 74% | 99% |
A0A3R7RKF3 | Trypanosoma rangeli | 36% | 100% |
A0A3S7XBW0 | Leishmania donovani | 94% | 100% |
A4HQ74 | Leishmania braziliensis | 81% | 98% |
A4IDX2 | Leishmania infantum | 95% | 100% |
D0A445 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q0K3 | Leishmania major | 93% | 100% |
V5B3M7 | Trypanosoma cruzi | 35% | 100% |