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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QAV9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.643 |
CLV_MEL_PAP_1 | 36 | 42 | PF00089 | 0.497 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.766 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.553 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.414 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.561 |
DOC_CKS1_1 | 273 | 278 | PF01111 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 272 | 279 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 33 | 40 | PF00069 | 0.517 |
DOC_MAPK_RevD_3 | 131 | 147 | PF00069 | 0.666 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.624 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.646 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 262 | 266 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 322 | 329 | PF00244 | 0.699 |
LIG_AP2alpha_2 | 224 | 226 | PF02296 | 0.694 |
LIG_BIR_III_4 | 152 | 156 | PF00653 | 0.799 |
LIG_Clathr_ClatBox_1 | 48 | 52 | PF01394 | 0.538 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.589 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.310 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.492 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.692 |
LIG_FXI_DFP_1 | 245 | 249 | PF00024 | 0.568 |
LIG_G3BP_FGDF_1 | 243 | 248 | PF02136 | 0.450 |
LIG_LIR_Gen_1 | 10 | 21 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 224 | 234 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 247 | 253 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.489 |
LIG_LIR_LC3C_4 | 256 | 261 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.432 |
LIG_LYPXL_S_1 | 285 | 289 | PF13949 | 0.451 |
LIG_LYPXL_yS_3 | 208 | 211 | PF13949 | 0.446 |
LIG_LYPXL_yS_3 | 286 | 289 | PF13949 | 0.437 |
LIG_NRBOX | 50 | 56 | PF00104 | 0.578 |
LIG_Pex14_2 | 307 | 311 | PF04695 | 0.509 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.580 |
LIG_SH2_SRC | 185 | 188 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.454 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.694 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.726 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.486 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.556 |
LIG_SUMO_SIM_anti_2 | 255 | 262 | PF11976 | 0.439 |
LIG_SUMO_SIM_anti_2 | 46 | 52 | PF11976 | 0.454 |
LIG_SUMO_SIM_anti_2 | 63 | 68 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 291 | 297 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 46 | 52 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 56 | 63 | PF11976 | 0.556 |
LIG_TYR_ITIM | 206 | 211 | PF00017 | 0.431 |
LIG_UBA3_1 | 111 | 119 | PF00899 | 0.559 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.538 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.501 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.522 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.392 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.665 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.681 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.683 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.481 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.480 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.545 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.522 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.697 |
MOD_PK_1 | 62 | 68 | PF00069 | 0.549 |
MOD_PKA_1 | 321 | 327 | PF00069 | 0.569 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.545 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.431 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.433 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.703 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.595 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.594 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.473 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.503 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.453 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.389 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.554 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.467 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.553 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.520 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.543 |
MOD_SUMO_rev_2 | 173 | 182 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.544 |
TRG_DiLeu_BaEn_1 | 31 | 36 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 284 | 289 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 271 | 274 | PF00400 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7K8 | Leptomonas seymouri | 68% | 100% |
A0A0S4JUQ7 | Bodo saltans | 39% | 100% |
A0A1X0NIQ0 | Trypanosomatidae | 46% | 100% |
A0A3Q8IBY8 | Leishmania donovani | 94% | 100% |
E9AH33 | Leishmania infantum | 94% | 100% |
E9AWL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |