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: A4HCP9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.559 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.767 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.765 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.690 |
CLV_PCSK_PC7_1 | 273 | 279 | PF00082 | 0.473 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.561 |
DEG_APCC_DBOX_1 | 182 | 190 | PF00400 | 0.458 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.529 |
DOC_AGCK_PIF_2 | 295 | 300 | PF00069 | 0.580 |
DOC_CKS1_1 | 133 | 138 | PF01111 | 0.389 |
DOC_MAPK_gen_1 | 208 | 217 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 59 | 68 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 211 | 219 | PF00069 | 0.755 |
DOC_MAPK_MEF2A_6 | 62 | 70 | PF00069 | 0.540 |
DOC_PP1_RVXF_1 | 176 | 182 | PF00149 | 0.550 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.598 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.521 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.680 |
DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.617 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.588 |
LIG_CAP-Gly_1 | 294 | 300 | PF01302 | 0.574 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.555 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.444 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.607 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.605 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.530 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.672 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.624 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.608 |
LIG_LIR_Apic_2 | 130 | 136 | PF02991 | 0.569 |
LIG_LIR_Apic_2 | 218 | 222 | PF02991 | 0.530 |
LIG_LIR_Apic_2 | 55 | 61 | PF02991 | 0.652 |
LIG_LIR_Apic_2 | 78 | 82 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 147 | 151 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.639 |
LIG_Pex14_1 | 148 | 152 | PF04695 | 0.416 |
LIG_SH2_GRB2like | 112 | 115 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.668 |
LIG_TRAF2_1 | 15 | 18 | PF00917 | 0.713 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.608 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.467 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.332 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.708 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.611 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.595 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.546 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.584 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.591 |
MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.744 |
MOD_Cter_Amidation | 27 | 30 | PF01082 | 0.654 |
MOD_Cter_Amidation | 32 | 35 | PF01082 | 0.657 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.705 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.690 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.713 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.729 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.476 |
MOD_LATS_1 | 281 | 287 | PF00433 | 0.740 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.659 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.469 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.310 |
MOD_PKA_1 | 34 | 40 | PF00069 | 0.689 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.726 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.684 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.523 |
MOD_Plk_2-3 | 125 | 131 | PF00069 | 0.493 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.579 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.428 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.704 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.584 |
MOD_SUMO_rev_2 | 142 | 147 | PF00179 | 0.347 |
MOD_SUMO_rev_2 | 261 | 270 | PF00179 | 0.444 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.528 |
TRG_NLS_Bipartite_1 | 196 | 215 | PF00514 | 0.460 |
TRG_NLS_MonoExtN_4 | 208 | 215 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P555 | Leptomonas seymouri | 58% | 86% |
A0A0S4IRA8 | Bodo saltans | 25% | 95% |
A0A1X0NX54 | Trypanosomatidae | 37% | 100% |
A0A3Q8IAW9 | Leishmania donovani | 73% | 100% |
A0A422NW66 | Trypanosoma rangeli | 42% | 100% |
A4I075 | Leishmania infantum | 73% | 100% |
C9ZUZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AW38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4QBD9 | Leishmania major | 71% | 100% |