Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: A4HV54
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 14 |
GO:0003677 | DNA binding | 4 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.483 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.432 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.614 |
DEG_APCC_DBOX_1 | 223 | 231 | PF00400 | 0.535 |
DOC_CDC14_PxL_1 | 143 | 151 | PF14671 | 0.609 |
DOC_CYCLIN_RxL_1 | 206 | 218 | PF00134 | 0.655 |
DOC_CYCLIN_RxL_1 | 44 | 56 | PF00134 | 0.401 |
DOC_PP1_RVXF_1 | 137 | 144 | PF00149 | 0.677 |
DOC_USP7_UBL2_3 | 265 | 269 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.519 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.444 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_deltaCOP1_diTrp_1 | 35 | 39 | PF00928 | 0.428 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.693 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.659 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 91 | 102 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.430 |
LIG_PTB_Apo_2 | 117 | 124 | PF02174 | 0.418 |
LIG_SH2_GRB2like | 128 | 131 | PF00017 | 0.526 |
LIG_SH2_PTP2 | 47 | 50 | PF00017 | 0.446 |
LIG_SH2_PTP2 | 69 | 72 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.402 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.651 |
LIG_SUMO_SIM_anti_2 | 225 | 231 | PF11976 | 0.644 |
LIG_SUMO_SIM_par_1 | 225 | 231 | PF11976 | 0.626 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.524 |
MOD_CDC14_SPxK_1 | 121 | 124 | PF00782 | 0.433 |
MOD_CDK_SPxK_1 | 118 | 124 | PF00069 | 0.433 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.649 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.418 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.507 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.524 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.433 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.391 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.666 |
MOD_LATS_1 | 247 | 253 | PF00433 | 0.451 |
MOD_LATS_1 | 5 | 11 | PF00433 | 0.562 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.664 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.524 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.409 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.418 |
MOD_NEK2_2 | 267 | 272 | PF00069 | 0.497 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.432 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.637 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.409 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.637 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.515 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.446 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.466 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.674 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.439 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.418 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.427 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.519 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.645 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 271 | 274 | PF00400 | 0.427 |
TRG_NES_CRM1_1 | 225 | 239 | PF08389 | 0.548 |
TRG_NLS_MonoExtC_3 | 190 | 196 | PF00514 | 0.679 |
TRG_NLS_MonoExtN_4 | 190 | 195 | PF00514 | 0.676 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 224 | 228 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5T3 | Leptomonas seymouri | 87% | 100% |
A0A0S4JCN1 | Bodo saltans | 26% | 90% |
A0A0S4JLV2 | Bodo saltans | 53% | 100% |
A0A1X0NMT4 | Trypanosomatidae | 68% | 100% |
A0A3R7KK47 | Trypanosoma rangeli | 68% | 100% |
A0A3S5H6K3 | Leishmania donovani | 100% | 100% |
A4H6S6 | Leishmania braziliensis | 92% | 99% |
C9ZQD1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
D0A9C1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 72% |
E9ANT7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4QGT3 | Leishmania major | 98% | 100% |
V5BHW6 | Trypanosoma cruzi | 66% | 100% |