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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4H659
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.520 |
CLV_Separin_Metazoa | 9 | 13 | PF03568 | 0.558 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.257 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.568 |
DEG_SPOP_SBC_1 | 25 | 29 | PF00917 | 0.569 |
DOC_CKS1_1 | 91 | 96 | PF01111 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 91 | 97 | PF00134 | 0.589 |
DOC_MAPK_FxFP_2 | 63 | 66 | PF00069 | 0.679 |
DOC_MAPK_gen_1 | 61 | 70 | PF00069 | 0.653 |
DOC_MAPK_HePTP_8 | 58 | 70 | PF00069 | 0.580 |
DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.698 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.750 |
DOC_USP7_UBL2_3 | 110 | 114 | PF12436 | 0.612 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.696 |
DOC_USP7_UBL2_3 | 376 | 380 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 12 | 22 | PF00244 | 0.775 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.396 |
LIG_Clathr_ClatBox_1 | 313 | 317 | PF01394 | 0.419 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.428 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.381 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.625 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.704 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.661 |
LIG_LIR_Gen_1 | 183 | 192 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 242 | 253 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.508 |
LIG_Pex14_1 | 287 | 291 | PF04695 | 0.357 |
LIG_PTB_Apo_2 | 287 | 294 | PF02174 | 0.436 |
LIG_PTB_Phospho_1 | 287 | 293 | PF10480 | 0.435 |
LIG_SH2_CRK | 192 | 196 | PF00017 | 0.497 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.195 |
LIG_SH2_GRB2like | 185 | 188 | PF00017 | 0.612 |
LIG_SH2_NCK_1 | 192 | 196 | PF00017 | 0.439 |
LIG_SH2_SRC | 318 | 321 | PF00017 | 0.195 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.537 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.648 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.589 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.676 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.306 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.495 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.817 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.434 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.423 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.649 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.761 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.710 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.400 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.597 |
MOD_GlcNHglycan | 123 | 128 | PF01048 | 0.430 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.483 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.287 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.363 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.812 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.718 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.434 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.475 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.644 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.762 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.763 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.299 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.317 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.318 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.274 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.585 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.783 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.671 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.740 |
MOD_PK_1 | 64 | 70 | PF00069 | 0.637 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.641 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.744 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.681 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.330 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.677 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.239 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.493 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.594 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.731 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.292 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.718 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.727 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.703 |
MOD_SUMO_for_1 | 38 | 41 | PF00179 | 0.568 |
TRG_DiLeu_BaEn_4 | 216 | 222 | PF01217 | 0.368 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.701 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILE4 | Leptomonas seymouri | 55% | 99% |
A0A0S4ILW7 | Bodo saltans | 47% | 100% |
A0A1X0NQ98 | Trypanosomatidae | 52% | 100% |
A0A3S5IS56 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WR67 | Leishmania donovani | 80% | 100% |
A4HUH9 | Leishmania infantum | 81% | 100% |
C9ZVK4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AN77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QHE8 | Leishmania major | 78% | 98% |
V5BP48 | Trypanosoma cruzi | 51% | 100% |