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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HQA0
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.470 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.491 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.601 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.740 |
DOC_ANK_TNKS_1 | 228 | 235 | PF00023 | 0.583 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.648 |
DOC_CKS1_1 | 317 | 322 | PF01111 | 0.715 |
DOC_CKS1_1 | 337 | 342 | PF01111 | 0.429 |
DOC_MAPK_gen_1 | 104 | 113 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 242 | 251 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.647 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.527 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.777 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.673 |
DOC_USP7_UBL2_3 | 173 | 177 | PF12436 | 0.603 |
DOC_USP7_UBL2_3 | 199 | 203 | PF12436 | 0.619 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 236 | 241 | PF00244 | 0.619 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.594 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.669 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.715 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.600 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.792 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.612 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.445 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 83 | 91 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.435 |
LIG_PDZ_Class_2 | 340 | 345 | PF00595 | 0.676 |
LIG_Rb_LxCxE_1 | 18 | 35 | PF01857 | 0.530 |
LIG_REV1ctd_RIR_1 | 85 | 94 | PF16727 | 0.337 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.618 |
LIG_SH3_1 | 151 | 157 | PF00018 | 0.749 |
LIG_SH3_2 | 146 | 151 | PF14604 | 0.769 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.602 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.600 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.734 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.744 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.535 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.645 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.557 |
LIG_UBA3_1 | 55 | 59 | PF00899 | 0.588 |
LIG_WRC_WIRS_1 | 284 | 289 | PF05994 | 0.546 |
MOD_CDC14_SPxK_1 | 10 | 13 | PF00782 | 0.412 |
MOD_CDK_SPK_2 | 99 | 104 | PF00069 | 0.611 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.425 |
MOD_CDK_SPxxK_3 | 99 | 106 | PF00069 | 0.553 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.798 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.739 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.571 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.756 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.726 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.725 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.352 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.547 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.599 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.553 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.793 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.450 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.595 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.790 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.778 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.484 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.735 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.549 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.744 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.712 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.821 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.804 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.735 |
MOD_LATS_1 | 136 | 142 | PF00433 | 0.451 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.492 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.794 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.554 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.553 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.804 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.622 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.508 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.743 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.583 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.467 |
MOD_PKB_1 | 236 | 244 | PF00069 | 0.633 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.499 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.466 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.546 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.464 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.702 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.686 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.568 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.767 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.744 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.736 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.783 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.676 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.425 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 262 | 265 | PF00179 | 0.462 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 162 | 170 | PF00179 | 0.537 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 229 | 232 | PF00400 | 0.589 |
TRG_NLS_Bipartite_1 | 138 | 155 | PF00514 | 0.724 |
TRG_NLS_MonoExtN_4 | 149 | 155 | PF00514 | 0.683 |
TRG_NLS_MonoExtN_4 | 165 | 172 | PF00514 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P908 | Leptomonas seymouri | 52% | 97% |
A0A1X0NMA4 | Trypanosomatidae | 32% | 100% |
A0A3Q8IGP8 | Leishmania donovani | 68% | 99% |
A4IDZ6 | Leishmania infantum | 68% | 99% |
D0A409 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AU18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 99% |
Q4Q0H7 | Leishmania major | 70% | 100% |