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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A4IDZ6
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 | 192 | 196 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.761 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.699 |
CLV_PCSK_PC7_1 | 173 | 179 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.478 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.551 |
DEG_SPOP_SBC_1 | 300 | 304 | PF00917 | 0.692 |
DOC_ANK_TNKS_1 | 231 | 238 | PF00023 | 0.538 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.533 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.579 |
DOC_MAPK_gen_1 | 104 | 113 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 139 | 147 | PF00069 | 0.592 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.723 |
DOC_USP7_UBL2_3 | 164 | 168 | PF12436 | 0.650 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 173 | 180 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 40 | 50 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.505 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_2 | 43 | 49 | PF00533 | 0.400 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.626 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.642 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.699 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.395 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.508 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.495 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.620 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.366 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 83 | 89 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.401 |
LIG_PDZ_Class_2 | 342 | 347 | PF00595 | 0.560 |
LIG_PTAP_UEV_1 | 153 | 158 | PF05743 | 0.506 |
LIG_PTB_Apo_2 | 92 | 99 | PF02174 | 0.376 |
LIG_Rb_LxCxE_1 | 18 | 35 | PF01857 | 0.493 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.481 |
LIG_SH3_1 | 151 | 157 | PF00018 | 0.614 |
LIG_SH3_2 | 146 | 151 | PF14604 | 0.623 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.537 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.685 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.596 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.711 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.591 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.496 |
LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.588 |
LIG_UBA3_1 | 55 | 59 | PF00899 | 0.454 |
MOD_CDK_SPK_2 | 332 | 337 | PF00069 | 0.599 |
MOD_CDK_SPK_2 | 99 | 104 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 99 | 106 | PF00069 | 0.463 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.660 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.681 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.695 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.778 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.643 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.355 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.526 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.518 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.377 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.443 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.645 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.687 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.726 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.686 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.506 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.636 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.732 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.754 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.714 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.448 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.758 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.565 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.471 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.644 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.534 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.576 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.345 |
MOD_PKA_1 | 152 | 158 | PF00069 | 0.513 |
MOD_PKA_1 | 202 | 208 | PF00069 | 0.676 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.429 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.515 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.714 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.565 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.723 |
MOD_PKB_1 | 239 | 247 | PF00069 | 0.571 |
MOD_PKB_1 | 39 | 47 | PF00069 | 0.335 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.457 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.587 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.520 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.676 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.716 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.717 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.652 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.554 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 271 | 278 | PF00179 | 0.664 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.621 |
TRG_NLS_Bipartite_1 | 151 | 170 | PF00514 | 0.719 |
TRG_NLS_MonoExtC_3 | 165 | 170 | PF00514 | 0.697 |
TRG_NLS_MonoExtN_4 | 149 | 155 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 164 | 170 | PF00514 | 0.718 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 241 | 246 | PF00026 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 248 | 253 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 48 | 52 | PF00026 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P908 | Leptomonas seymouri | 47% | 97% |
A0A1X0NMA4 | Trypanosomatidae | 28% | 100% |
A0A3Q8IGP8 | Leishmania donovani | 100% | 100% |
A0A3R7NVJ3 | Trypanosoma rangeli | 29% | 100% |
A4HQA0 | Leishmania braziliensis | 68% | 99% |
D0A409 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AU18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q0H7 | Leishmania major | 88% | 100% |