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: Q4Q8P5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.501 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 184 | 186 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.501 |
CLV_PCSK_PC7_1 | 180 | 186 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 196 | 202 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.489 |
DOC_AGCK_PIF_1 | 111 | 116 | PF00069 | 0.342 |
DOC_CKS1_1 | 226 | 231 | PF01111 | 0.650 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.299 |
DOC_PP4_FxxP_1 | 282 | 285 | PF00568 | 0.677 |
DOC_SPAK_OSR1_1 | 136 | 140 | PF12202 | 0.412 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.523 |
DOC_USP7_MATH_2 | 211 | 217 | PF00917 | 0.481 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.299 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 136 | 142 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 111 | 129 | PF00022 | 0.412 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.566 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 133 | 137 | PF00533 | 0.412 |
LIG_deltaCOP1_diTrp_1 | 197 | 202 | PF00928 | 0.474 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.595 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.554 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.643 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.578 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.255 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.564 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.524 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.573 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.514 |
LIG_HCF-1_HBM_1 | 60 | 63 | PF13415 | 0.540 |
LIG_IBAR_NPY_1 | 241 | 243 | PF08397 | 0.523 |
LIG_LIR_Apic_2 | 281 | 285 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 70 | 76 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.311 |
LIG_PCNA_PIPBox_1 | 156 | 165 | PF02747 | 0.319 |
LIG_PDZ_Class_1 | 292 | 297 | PF00595 | 0.595 |
LIG_Pex14_1 | 198 | 202 | PF04695 | 0.467 |
LIG_Pex14_1 | 226 | 230 | PF04695 | 0.530 |
LIG_Pex14_2 | 137 | 141 | PF04695 | 0.466 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.596 |
LIG_PTB_Apo_2 | 238 | 245 | PF02174 | 0.529 |
LIG_PTB_Apo_2 | 65 | 72 | PF02174 | 0.516 |
LIG_PTB_Phospho_1 | 65 | 71 | PF10480 | 0.514 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.638 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.639 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.490 |
LIG_SH2_GRB2like | 71 | 74 | PF00017 | 0.533 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.299 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.680 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.546 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.540 |
LIG_TYR_ITSM | 226 | 233 | PF00017 | 0.623 |
LIG_WRC_WIRS_1 | 138 | 143 | PF05994 | 0.368 |
MOD_CDK_SPxK_1 | 245 | 251 | PF00069 | 0.509 |
MOD_CDK_SPxxK_3 | 266 | 273 | PF00069 | 0.614 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.308 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.388 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.474 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.637 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.602 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.255 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.582 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.426 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.462 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.622 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.685 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.329 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.652 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.609 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.426 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.589 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.480 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.631 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.414 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.244 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.253 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.388 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.473 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.638 |
MOD_NEK2_2 | 152 | 157 | PF00069 | 0.344 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.358 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.299 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.476 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.642 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.586 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.434 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.319 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.412 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.640 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.400 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.682 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.299 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.299 |
MOD_SUMO_for_1 | 264 | 267 | PF00179 | 0.606 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.627 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.543 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILT8 | Leptomonas seymouri | 69% | 99% |
A0A0S4IUG6 | Bodo saltans | 51% | 100% |
A0A1X0NVZ8 | Trypanosomatidae | 64% | 100% |
A0A3S7X178 | Leishmania donovani | 99% | 100% |
A4HG66 | Leishmania braziliensis | 92% | 100% |
A4I3A9 | Leishmania infantum | 98% | 100% |
D0A7S5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9AZI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5DAH1 | Trypanosoma cruzi | 64% | 100% |