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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IBQ4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.508 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.689 |
DOC_CYCLIN_yCln2_LP_2 | 278 | 284 | PF00134 | 0.323 |
DOC_MAPK_MEF2A_6 | 200 | 209 | PF00069 | 0.411 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 66 | 70 | PF00244 | 0.641 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.627 |
LIG_BIR_III_4 | 276 | 280 | PF00653 | 0.348 |
LIG_BRCT_BRCA1_1 | 259 | 263 | PF00533 | 0.324 |
LIG_deltaCOP1_diTrp_1 | 99 | 109 | PF00928 | 0.325 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.433 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.587 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.699 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.388 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.263 |
LIG_LIR_Apic_2 | 135 | 139 | PF02991 | 0.392 |
LIG_LIR_Apic_2 | 172 | 177 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 190 | 201 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 214 | 222 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.480 |
LIG_MYND_1 | 60 | 64 | PF01753 | 0.483 |
LIG_NRBOX | 22 | 28 | PF00104 | 0.346 |
LIG_PCNA_PIPBox_1 | 144 | 153 | PF02747 | 0.407 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.393 |
LIG_PTB_Apo_2 | 277 | 284 | PF02174 | 0.385 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.400 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.353 |
LIG_SH2_GRB2like | 174 | 177 | PF00017 | 0.423 |
LIG_SH2_GRB2like | 193 | 196 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 136 | 140 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 174 | 178 | PF00017 | 0.426 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.402 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.340 |
LIG_SUMO_SIM_par_1 | 290 | 298 | PF11976 | 0.341 |
MOD_CDK_SPK_2 | 33 | 38 | PF00069 | 0.486 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.557 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.455 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.473 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.393 |
MOD_Cter_Amidation | 86 | 89 | PF01082 | 0.532 |
MOD_DYRK1A_RPxSP_1 | 217 | 221 | PF00069 | 0.338 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.441 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.338 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.538 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.479 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.453 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.601 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.297 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.522 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.425 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.480 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.418 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.439 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.391 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.446 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.540 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.382 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.582 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.690 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.511 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.337 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.342 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.387 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.401 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.428 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.433 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.630 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.629 |
MOD_PKB_1 | 89 | 97 | PF00069 | 0.474 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.458 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.473 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.321 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.440 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.370 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.447 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.537 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.519 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.316 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Z2 | Leptomonas seymouri | 45% | 100% |
A0A1X0P8Z8 | Trypanosomatidae | 27% | 92% |
A4H3R5 | Leishmania braziliensis | 64% | 100% |
A4I4Y4 | Leishmania infantum | 100% | 100% |
C9ZKJ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 93% |
E9AEE6 | Leishmania major | 84% | 100% |
E9ALE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
V5BSV9 | Trypanosoma cruzi | 37% | 100% |