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: Q4Q0K3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.774 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.730 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.460 |
DEG_SPOP_SBC_1 | 188 | 192 | PF00917 | 0.757 |
DOC_CYCLIN_RxL_1 | 43 | 53 | PF00134 | 0.552 |
DOC_MAPK_gen_1 | 43 | 52 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 214 | 222 | PF00069 | 0.541 |
DOC_MIT_MIM_1 | 7 | 17 | PF04212 | 0.450 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.431 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.757 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 338 | 343 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.400 |
LIG_Actin_WH2_2 | 191 | 206 | PF00022 | 0.687 |
LIG_APCC_ABBA_1 | 331 | 336 | PF00400 | 0.620 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.529 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.601 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.424 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.485 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.716 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.606 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.694 |
LIG_LIR_Gen_1 | 157 | 162 | PF02991 | 0.716 |
LIG_LIR_Gen_1 | 172 | 179 | PF02991 | 0.728 |
LIG_LIR_Gen_1 | 276 | 286 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 325 | 334 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.602 |
LIG_MYND_1 | 201 | 205 | PF01753 | 0.682 |
LIG_Pex14_2 | 261 | 265 | PF04695 | 0.536 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.629 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.716 |
LIG_SH2_GRB2like | 279 | 282 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.489 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.554 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.716 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.579 |
LIG_SH2_STAT3 | 307 | 310 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.533 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.711 |
LIG_SUMO_SIM_anti_2 | 174 | 180 | PF11976 | 0.757 |
LIG_SUMO_SIM_anti_2 | 6 | 12 | PF11976 | 0.448 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 99 | 104 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 76 | 83 | PF11976 | 0.524 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.547 |
LIG_TRAF2_1 | 352 | 355 | PF00917 | 0.632 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.718 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.719 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.469 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.522 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.784 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.524 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.593 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.632 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.760 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.551 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.513 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.566 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.661 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.692 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.553 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.606 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.430 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.625 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.606 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.483 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.671 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.406 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.371 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.692 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.563 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.726 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.473 |
MOD_PKA_1 | 312 | 318 | PF00069 | 0.590 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.398 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.725 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.673 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.462 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.561 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.567 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.639 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.546 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.523 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.486 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.700 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.754 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.719 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.435 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.634 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.517 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.506 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.523 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.719 |
MOD_SUMO_for_1 | 352 | 355 | PF00179 | 0.690 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.395 |
TRG_DiLeu_BaEn_4 | 146 | 152 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.716 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.651 |
TRG_Pf-PMV_PEXEL_1 | 48 | 53 | PF00026 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P9D5 | Leptomonas seymouri | 73% | 99% |
A0A3R7RKF3 | Trypanosoma rangeli | 36% | 100% |
A0A3S7XBW0 | Leishmania donovani | 94% | 100% |
A4HQ74 | Leishmania braziliensis | 81% | 100% |
A4IDX2 | Leishmania infantum | 95% | 100% |
D0A445 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ATZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5B3M7 | Trypanosoma cruzi | 36% | 100% |