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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005743 | mitochondrial inner membrane | 5 | 5 |
GO:0019866 | organelle inner membrane | 4 | 5 |
GO:0031090 | organelle membrane | 3 | 5 |
GO:0031966 | mitochondrial membrane | 4 | 5 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8ID19
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 5 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 5 |
GO:0006878 | intracellular copper ion homeostasis | 8 | 5 |
GO:0008535 | respiratory chain complex IV assembly | 7 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0017004 | cytochrome complex assembly | 6 | 6 |
GO:0019725 | cellular homeostasis | 2 | 5 |
GO:0022607 | cellular component assembly | 4 | 6 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 5 |
GO:0033108 | mitochondrial respiratory chain complex assembly | 6 | 2 |
GO:0033617 | mitochondrial cytochrome c oxidase assembly | 7 | 2 |
GO:0042592 | homeostatic process | 3 | 5 |
GO:0043933 | protein-containing complex organization | 4 | 6 |
GO:0046916 | obsolete intracellular transition metal ion homeostasis | 7 | 5 |
GO:0048878 | chemical homeostasis | 4 | 5 |
GO:0050801 | monoatomic ion homeostasis | 5 | 5 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 5 |
GO:0055070 | copper ion homeostasis | 9 | 5 |
GO:0055076 | obsolete transition metal ion homeostasis | 8 | 5 |
GO:0055080 | monoatomic cation homeostasis | 6 | 5 |
GO:0055082 | intracellular chemical homeostasis | 3 | 5 |
GO:0065003 | protein-containing complex assembly | 5 | 6 |
GO:0065007 | biological regulation | 1 | 5 |
GO:0065008 | regulation of biological quality | 2 | 5 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
GO:0098771 | inorganic ion homeostasis | 6 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0005488 | binding | 1 | 5 |
GO:0005507 | copper ion binding | 6 | 5 |
GO:0016491 | oxidoreductase activity | 2 | 4 |
GO:0016530 | metallochaperone activity | 2 | 5 |
GO:0016531 | copper chaperone activity | 3 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
GO:0046914 | transition metal ion binding | 5 | 5 |
GO:0140104 | molecular carrier activity | 1 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.403 |
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.371 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.674 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.437 |
CLV_PCSK_FUR_1 | 180 | 184 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.658 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.415 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.674 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 398 | 407 | PF00134 | 0.634 |
DOC_MAPK_gen_1 | 180 | 188 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 227 | 235 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 227 | 235 | PF00069 | 0.504 |
DOC_MAPK_RevD_3 | 168 | 183 | PF00069 | 0.293 |
DOC_PP1_RVXF_1 | 311 | 317 | PF00149 | 0.456 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.616 |
DOC_PP4_FxxP_1 | 316 | 319 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.390 |
DOC_USP7_UBL2_3 | 256 | 260 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 145 | 154 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.429 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.576 |
LIG_CtBP_PxDLS_1 | 245 | 249 | PF00389 | 0.470 |
LIG_deltaCOP1_diTrp_1 | 265 | 271 | PF00928 | 0.456 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.732 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.344 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.467 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.364 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.364 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.481 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.459 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.512 |
LIG_LIR_Apic_2 | 197 | 201 | PF02991 | 0.710 |
LIG_LIR_Apic_2 | 265 | 269 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 351 | 360 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.477 |
LIG_PCNA_PIPBox_1 | 251 | 260 | PF02747 | 0.470 |
LIG_Pex14_1 | 163 | 167 | PF04695 | 0.311 |
LIG_Pex14_1 | 230 | 234 | PF04695 | 0.499 |
LIG_Pex14_1 | 267 | 271 | PF04695 | 0.456 |
LIG_Pex14_1 | 356 | 360 | PF04695 | 0.492 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.420 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.612 |
LIG_SUMO_SIM_par_1 | 173 | 178 | PF11976 | 0.278 |
LIG_SUMO_SIM_par_1 | 211 | 217 | PF11976 | 0.551 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.595 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.656 |
LIG_UBA3_1 | 270 | 277 | PF00899 | 0.484 |
LIG_WRC_WIRS_1 | 195 | 200 | PF05994 | 0.704 |
MOD_CDC14_SPxK_1 | 76 | 79 | PF00782 | 0.387 |
MOD_CDK_SPK_2 | 289 | 294 | PF00069 | 0.515 |
MOD_CDK_SPxK_1 | 277 | 283 | PF00069 | 0.456 |
MOD_CDK_SPxK_1 | 73 | 79 | PF00069 | 0.390 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.506 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.736 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.540 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.458 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.604 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.509 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.415 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.416 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.456 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.509 |
MOD_CMANNOS | 160 | 163 | PF00535 | 0.293 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.273 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.706 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.594 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.635 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.384 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.297 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.602 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.797 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.511 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.440 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.483 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.558 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.478 |
MOD_NEK2_2 | 426 | 431 | PF00069 | 0.755 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.385 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.456 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.591 |
MOD_PKA_1 | 219 | 225 | PF00069 | 0.470 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.406 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.465 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.535 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.443 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.505 |
MOD_Plk_2-3 | 322 | 328 | PF00069 | 0.470 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.371 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.464 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.601 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.614 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.456 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.509 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.508 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.577 |
MOD_SUMO_rev_2 | 184 | 192 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 405 | 415 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 2 | 7 | PF01217 | 0.613 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.488 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 4 | 9 | PF00026 | 0.417 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2G6 | Leptomonas seymouri | 84% | 100% |
A0A1X0P7F2 | Trypanosomatidae | 70% | 98% |
A0A3R7N2E4 | Trypanosoma rangeli | 66% | 100% |
A0A3S5H5E9 | Leishmania donovani | 38% | 100% |
A4H427 | Leishmania braziliensis | 38% | 100% |
A4HF41 | Leishmania braziliensis | 92% | 100% |
A4HSB1 | Leishmania infantum | 38% | 100% |
A4I2C5 | Leishmania infantum | 100% | 100% |
C9ZX87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9AK94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AYH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O97196 | Leishmania major | 39% | 100% |
Q4Q8Z5 | Leishmania major | 97% | 100% |
V5BA25 | Trypanosoma cruzi | 64% | 100% |