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: 12 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: A4HMT5
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 13 |
GO:0016043 | cellular component organization | 3 | 13 |
GO:0022607 | cellular component assembly | 4 | 13 |
GO:0043933 | protein-containing complex organization | 4 | 13 |
GO:0051259 | protein complex oligomerization | 6 | 13 |
GO:0051260 | protein homooligomerization | 7 | 13 |
GO:0065003 | protein-containing complex assembly | 5 | 13 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.427 |
CLV_PCSK_FUR_1 | 327 | 331 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.449 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.615 |
DEG_APCC_DBOX_1 | 351 | 359 | PF00400 | 0.518 |
DOC_CDC14_PxL_1 | 183 | 191 | PF14671 | 0.423 |
DOC_CYCLIN_RxL_1 | 326 | 336 | PF00134 | 0.504 |
DOC_MAPK_gen_1 | 216 | 225 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 317 | 325 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 329 | 339 | PF00069 | 0.375 |
DOC_PP1_RVXF_1 | 327 | 334 | PF00149 | 0.355 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.299 |
DOC_SPAK_OSR1_1 | 104 | 108 | PF12202 | 0.346 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.597 |
DOC_USP7_UBL2_3 | 317 | 321 | PF12436 | 0.388 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 104 | 108 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 12 | 21 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 235 | 241 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 320 | 326 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.344 |
LIG_Actin_WH2_2 | 318 | 334 | PF00022 | 0.416 |
LIG_BIR_III_4 | 23 | 27 | PF00653 | 0.639 |
LIG_BRCT_BRCA1_1 | 15 | 19 | PF00533 | 0.773 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.381 |
LIG_deltaCOP1_diTrp_1 | 128 | 137 | PF00928 | 0.346 |
LIG_eIF4E_1 | 163 | 169 | PF01652 | 0.376 |
LIG_eIF4E_1 | 184 | 190 | PF01652 | 0.346 |
LIG_eIF4E_1 | 247 | 253 | PF01652 | 0.327 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.335 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.346 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.299 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.355 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.433 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.474 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.488 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.459 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.521 |
LIG_LIR_Apic_2 | 103 | 108 | PF02991 | 0.301 |
LIG_LIR_Apic_2 | 129 | 135 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 299 | 307 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.525 |
LIG_NRBOX | 65 | 71 | PF00104 | 0.493 |
LIG_PTB_Apo_2 | 279 | 286 | PF02174 | 0.508 |
LIG_PTB_Apo_2 | 294 | 301 | PF02174 | 0.509 |
LIG_PTB_Phospho_1 | 279 | 285 | PF10480 | 0.502 |
LIG_RPA_C_Fungi | 37 | 49 | PF08784 | 0.518 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.346 |
LIG_SH2_GRB2like | 165 | 168 | PF00017 | 0.349 |
LIG_SH2_GRB2like | 280 | 283 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.328 |
LIG_SUMO_SIM_anti_2 | 228 | 233 | PF11976 | 0.450 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.411 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.427 |
LIG_TRAF2_1 | 361 | 364 | PF00917 | 0.431 |
MOD_CDC14_SPxK_1 | 211 | 214 | PF00782 | 0.551 |
MOD_CDK_SPxK_1 | 208 | 214 | PF00069 | 0.544 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.354 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.684 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.533 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.738 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.516 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.420 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.531 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.495 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.419 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.423 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.722 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.458 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.452 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.560 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.489 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.684 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.721 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.354 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.270 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.612 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.396 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.499 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.397 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.431 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.385 |
MOD_PKB_1 | 330 | 338 | PF00069 | 0.490 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.423 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.453 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.296 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.395 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.453 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.489 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.571 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.759 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.597 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.565 |
MOD_SUMO_for_1 | 137 | 140 | PF00179 | 0.423 |
MOD_SUMO_for_1 | 78 | 81 | PF00179 | 0.556 |
TRG_DiLeu_BaEn_2 | 295 | 301 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.141 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 342 | 345 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C7 | Leptomonas seymouri | 71% | 79% |
A0A0S4J5F7 | Bodo saltans | 43% | 98% |
A0A0S4JC91 | Bodo saltans | 43% | 98% |
A0A1X0P5J3 | Trypanosomatidae | 49% | 70% |
A0A3Q8II33 | Leishmania donovani | 94% | 88% |
A0A422P2R6 | Trypanosoma rangeli | 47% | 71% |
A4IBD6 | Leishmania infantum | 94% | 88% |
C9ZZ82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 70% |
E9AF92 | Leishmania major | 95% | 100% |
E9B6E7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 88% |
V5DUU9 | Trypanosoma cruzi | 48% | 71% |