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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4IBD6
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0022607 | cellular component assembly | 4 | 11 |
GO:0043933 | protein-containing complex organization | 4 | 11 |
GO:0051259 | protein complex oligomerization | 6 | 11 |
GO:0051260 | protein homooligomerization | 7 | 11 |
GO:0065003 | protein-containing complex assembly | 5 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.756 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.411 |
CLV_PCSK_FUR_1 | 377 | 381 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.614 |
DEG_APCC_DBOX_1 | 263 | 271 | PF00400 | 0.526 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.509 |
DOC_CDC14_PxL_1 | 233 | 241 | PF14671 | 0.420 |
DOC_CYCLIN_RxL_1 | 376 | 386 | PF00134 | 0.498 |
DOC_MAPK_gen_1 | 266 | 275 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 379 | 389 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 141 | 150 | PF00069 | 0.528 |
DOC_PP1_RVXF_1 | 377 | 384 | PF00149 | 0.376 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.291 |
DOC_SPAK_OSR1_1 | 154 | 158 | PF12202 | 0.388 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.595 |
DOC_USP7_UBL2_3 | 367 | 371 | PF12436 | 0.377 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.780 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 382 | 388 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 62 | 67 | PF00244 | 0.649 |
LIG_Actin_WH2_2 | 368 | 384 | PF00022 | 0.468 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.602 |
LIG_BIR_III_4 | 73 | 77 | PF00653 | 0.676 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.780 |
LIG_deltaCOP1_diTrp_1 | 178 | 187 | PF00928 | 0.388 |
LIG_eIF4E_1 | 213 | 219 | PF01652 | 0.370 |
LIG_eIF4E_1 | 234 | 240 | PF01652 | 0.388 |
LIG_eIF4E_1 | 297 | 303 | PF01652 | 0.312 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.303 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.388 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.319 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.326 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.436 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.458 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.553 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.426 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.553 |
LIG_LIR_Apic_2 | 153 | 158 | PF02991 | 0.294 |
LIG_LIR_Apic_2 | 179 | 185 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 311 | 322 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 349 | 357 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.335 |
LIG_NRBOX | 115 | 121 | PF00104 | 0.525 |
LIG_PTB_Apo_2 | 329 | 336 | PF02174 | 0.500 |
LIG_PTB_Apo_2 | 344 | 351 | PF02174 | 0.499 |
LIG_PTB_Phospho_1 | 329 | 335 | PF10480 | 0.493 |
LIG_RPA_C_Fungi | 87 | 99 | PF08784 | 0.550 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.388 |
LIG_SH2_GRB2like | 215 | 218 | PF00017 | 0.420 |
LIG_SH2_GRB2like | 330 | 333 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.360 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.653 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 278 | 283 | PF11976 | 0.476 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.385 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.388 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.419 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.545 |
MOD_CDC14_SPxK_1 | 261 | 264 | PF00782 | 0.503 |
MOD_CDK_SPxK_1 | 258 | 264 | PF00069 | 0.498 |
MOD_CDK_SPxxK_3 | 22 | 29 | PF00069 | 0.733 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.501 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.693 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.518 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.632 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.712 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.406 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.524 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.655 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.636 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.459 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.533 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.452 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.553 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.403 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.662 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.459 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.611 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.443 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.703 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.539 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.644 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.417 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.367 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.343 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.722 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.600 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.388 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.728 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.369 |
MOD_PKB_1 | 380 | 388 | PF00069 | 0.477 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.420 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.477 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.448 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.341 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.475 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.477 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.687 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.607 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.563 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.782 |
MOD_SUMO_for_1 | 128 | 131 | PF00179 | 0.570 |
MOD_SUMO_for_1 | 187 | 190 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 122 | 128 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_2 | 345 | 351 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.150 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C7 | Leptomonas seymouri | 68% | 89% |
A0A1X0P5J3 | Trypanosomatidae | 49% | 80% |
A0A3Q8II33 | Leishmania donovani | 100% | 100% |
A0A422P2R6 | Trypanosoma rangeli | 47% | 81% |
A4HMT5 | Leishmania braziliensis | 94% | 100% |
C9ZZ82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 80% |
E9AF92 | Leishmania major | 97% | 100% |
E9B6E7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5DUU9 | Trypanosoma cruzi | 49% | 81% |